<![CDATA[Bayside Solutions: jobboards]]> http://JOBS.BAYSIDESOLUTIONS.COM/ en-us <![CDATA[BioSpecimen Management Scientist I]]> Bayside Solutions is seeking a  BioSpecimen Management Scientist I to be part of our client’ s team in the East Bay Area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

BSM Scientist I

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Works independently to deliver simple, efficient solutions, facilitating receipt of shipments of human biological samples, verify sample integrity and data accuracy, process (centrifuge, aliquot, and pool) samples, consolidate inventory, retrieve and distribute samples, maintain inventory of supplies and ships supplies and facilitate routine activities in the build of custom panels, in close communication with team members.
  • Assumes responsibility for the accuracy, quality, and timeliness of all assigned projects, tasks and related activities, and keeps supervisor informed of project status. 
  • Assumes accountability for electronic records management and use of validated systems ensuring information is maintained in a timely manner, accurately and consistently.
  • Follows good practices in their daily tasks.

Summary of Qualifications:
  • Associate degree or certification in Biological Science or related field, or equivalent combination of education and work experience.  
  • 1+-years of related experience required, including at least 6 months of handling biological samples.
  • Understanding of good laboratory, data and documentation practices a must.
  • Experience with basic computer applications a must.
  • Ability to work in low temperatures environment, with human biological samples.
  • Ability to lift objects up to 30 lbs.
  • Good organizational, written and verbal communication and cross-functional participation skills.
  • Adaptable and meticulous; Able to work in dynamic and matrix environment, and capable of handling multiple projects.
  • Understands the importance and impact of biospecimens in research; Results and goals oriented.
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Mon, 13 Aug 2018 00:00:00 PDT 0
<![CDATA[Senior Scientist]]> Bayside Solutions is seeking a  Senior Scientist to be part of our client’ s team in the South Bay. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Senior Scientist

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Works under minimal supervision, to conduct laboratory experiments utilizing established and published procedures with advanced technical and theoretical understanding.
  • Makes recommendations to resolve problems encountered during experimental procedures.
  • Assumes responsibility for the accuracy, quality, and timeliness of experimental results.
  • Summarizes experimental results, and reviews conclusions with supervisor/project leader.
  • Communicates results of experiments in the form of reports and presentations.
  • Keeps supervisor/project leader informed of project status, particularly of significant findings and results in critical problem areas.
  • Performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g., OSHA).
  • Accurately and consistently records experimental methods, materials, and results.
  • Applies advanced technical writing skills to produce reports and documents such as summaries, SOPs, DHFs, presentations and manuscripts.
  • Participates in routine lab maintenance, lab safety, ISO, and QSR implementation.

Summary of Qualifications:
  • Bachelor’ s degree in Biological/Life Sciences, Chemistry, Biochemistry or related field, or equivalent combination of education and work-related experience.
  • Minimum of 7 - 10 years of relevant industry experience is required.
  • Ability to design and execute relevant laboratory experimentation and determine next steps within the context of overall project goals and direction.
  • Background and technique skills in biochemistry and molecular biology.
  • Hands-on experiences with PCR, and/or Microarray, and/or NGS technology. 
  • Good understanding of bioinformatics and biostatistics.
  • Good data analysis skills and good documentation skills.
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Mon, 13 Aug 2018 00:00:00 PDT 0
<![CDATA[Labware Technician]]> Bayside Solutions is seeking a Labware Technician to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Labware Technician

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Support the shared manufacturing services department by working effectively within the group to meet department goals, objectives and tasks to achieve the desired results.
  • Work with Supervisor and Lead to prioritize tasks and assignments and make recommendations to maximize efficiency and productivity based on shift needs.
  • Follow department policies and adhere to the clients Good Document Practices.
  • Support the SMS values of Execution, Unity, and Resilience.
  • Work with senior technicians and leads to prioritize tasks, assignments, and make recommendations to maximize efficiency and productivity based on shift needs.
  • Rigorous inventory management and ability to communicate with customers in a professional manner.
  • Support the shift by completing required training in all areas of Equipment Preparation, Stock Solutions, and Preweigh within the specified training curriculum.
  • Responsible for cleaning, sterilizing, and prepping glassware and parts used in the manufacturing environment.
  • Accountable for completing all assigned tasks, which include media preparation, filtration, sterile pipetting, CIP, SIP, sub-aliquoting powders liquids into smaller containers while working with an ERP system and an MES system.
  • Obtain materials for manufacturing operations, and follow a production schedule.
  • This position requires working within a cGMP facility and the technician will be required to wear a plant dedicated uniform (polyester) and a full coverall (Tyvek – flashspun high-density polyethylene fibers) over the plant uniform.
  • No makeup or nail polish is allowed when gowned.
  • Technician must be able to use hand sanitizer (alcohol), hair/beard covers, and be comfortable with working with and around powered industrial trucks (motorized pallet jacks).

Summary of Qualifications:
  • Minimum of a high school degree with some college-level course work in biological science, physical sciences or at least 2 years of relevant experience; BA/BS in life/physical sciences or equivalent preferred.
  • Must possess good problem solving, mechanical aptitude, interpersonal communication and team skills.
  • Must be a self-starter with strong focus on quality, details and results.
  • Possess effective time management and organizational skills.
  • Must be able to be flexible in work assignments, work weekends, off shifts and overtime as required.
  • Possess proficiency in business applications including inventory control systems. 
  • Must be able to lift up to 40 lbs and stand for extended periods of time.
  • Technician must have a high standard for safety and the highest level of attention to detail.
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Mon, 13 Aug 2018 00:00:00 PDT 0
<![CDATA[Research Associate, Histology]]> Bayside Solutions is seeking a Research Associate, Histology to be part of our client’ s team in Redwood City. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate, Histology:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Responsible for tissue processing (FFPE and fresh frozen) and slide preparation.
  • Proper maintenance/tracking of collected samples and slides.
  • Conduct immunohistochemical and immunofluorescent staining on mammalian tissue sections.
  • Produce experimental results using microscopy.
  • Coordinate activities with project team members.
  • Collaborate with project team members to discuss experiments and data.
  • General lab duties such as preparation of reagents and stocking of supplies.
  • Follow laboratory safety guidelines and practices.

Summary of Qualifications:
  • Bachelors of Science or Masters in biology or related discipline with at least 2 years of lab experience.
  • Experience in tissue processing, histological slide preparation, and immunohistochemical and immunofluorescent staining in mammalian tissues required.
  • Must have excellent organization and planning skills and the ability to work under timeline in a fast-paced environment.
  • Excellent written and oral communication skills.
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Mon, 13 Aug 2018 00:00:00 PDT 0
<![CDATA[Quality Systems Specialist]]> Bayside Solutions is seeking a Quality Systems Specialist to be part of our client’ s team in the Fremont area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Quality Systems Specialist

Job Benefits:
  • An opportunity to join a genomics sequencing organization. 
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Facilitate / lead risk assessments and author summary report.
  • Use ICH Q9 / ISO 14971 principles and risk management methods / tools to facilitate risk assessments (e.g. FMEA, Fault Tree Analysis, etc.).
  • Proactively leads initiatives to improve quality systems in the organization (for example, developing SOPs and KPIs for the business).
  • Identifies, designs, and implements process and system improvements.
  • Preparation for Metric / Management Reviews – Compile metrics, create slide decks and update performance boards.
  • Supports initiatives to improve quality systems in the organization.
  • Implements process and system improvements.
  • Maintain and make improvements to Quality Risk Management share room and associated QRM resources (e.g. Risk Registry, Periodic Review tracker, etc.).
  • Author and revise QRM work instructions, and risk assessment and summary report templates.
  • Perform other administrative duties in support of the QRM program as needed.

Required Qualifications:
  • Requires a Bachelor' s degree, from an accredited institution, in Microbiology, Biology, Chemistry (Or closely related degree with these core courses as the foundation).
  • Requires 6-8 years of pharmaceutical Quality Assurance / Systems experience.
  • Practical knowledge of ICH Q9 and ISO 14971.
  • Experience facilitating and leading risk assessments using risk management methods and tools.
  • Experience leading projects with history of achieving results and outstanding outcomes; must possess strong organizational skills and be able to self-motivate and work independently.
  • Solid knowledge of relevant regulations and guidance required in order to act as a resource for colleagues.
  • Must possess excellent verbal and written communication skills; strong interpersonal skills absolutely required.
  • Familiarity with Quality Management Systems and related regulatory guidelines.
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Mon, 13 Aug 2018 00:00:00 PDT 0
<![CDATA[Process Scientist II]]> Bayside Solutions is seeking a Process Scientist II to be part of our client’ s team in the Fremont area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Process Scientist II

Job Benefits:
  • An opportunity to join a genomics sequencing organization. 
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Candidate must have strong protein purification skills to perform developmental scientific work in support of an innovative project under the supervision of a Senior Scientist.
  • The role will function within the Protein Science group at the client’ s site alongside a team of other scientists, engineers, post-doctoral students, and interns with a wide spectrum of skill sets.
  • The position will apply scientific principles, process knowledge and independent thinking to lead an innovation project.
  • The day to day scientific duties of the position will be to perform literature search, design and execute experiments, analyze data, document experiments, build process economics model and predictive mathematical model.
  • The position may interface with other functional team such as bioprocess engineering group to contribute to continuous processing platform.

Required Qualifications:
  • M.S. with 2+ experience or Ph.D. with 0 years of experience from an accredited institution in biotechnology, chemical engineering, or biological / pharmaceutical sciences required.
  • Experience with UFDF or related membrane filtration is desirable.
  • Prior experience of modeling is a plus.
  • Computational skills of Matlab or related software is a plus
  • Good written and oral communication skills.
  • Ability to work in a team environment.
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Mon, 13 Aug 2018 00:00:00 PDT 0
<![CDATA[Project Coordinator II]]> Bayside Solutions is seeking Project Coordinator II to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Project Coordinator II

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Responsible for creating and maintaining Project Team master calendars.
  • Responsible for creating and maintaining Project Team distribution lists.
  • Extensive calendaring and meeting coordination, for Project Team as well as assigned key project team members.
  • Arranges and coordinates logistical support for meetings, events, and activities both on and off-site.
  • Travel arrangement preparation, including pro-active calendaring of complex meetings, including being the point of contact for guests and presenters.
  • Processing of assigned team members’ expense reports.
  • Responsible for working with Project Management to coordinate and minute regularly scheduled Project team meetings, including preparation of agendas, capturing and issuance of meeting minutes.
  • Order catering and office supplies for a variety of meetings and events, greet visitors, disseminate information.
  • Ensures the purchase of required office, computer, and telecommunications equipment to support the Project Team.
  • Assist in planning of teambuilding and collaboration activities for the Project Team
  • Identify and anticipate needs of the group and plan work activities accordingly.
  • Look for areas of activity overlap with co-workers and leverage resources to maximize time, resources and dissemination of information.
  • Additional responsibilities include filing, photocopying and distribution of documents, disseminating of incoming mail, and generally providing administrative assistance as necessary.

Required Qualifications:
  • Bachelor’ s degree is highly preferred or an AA degree with equivalent experience required.
  • 5+ years’ experience as a senior level administrative assistant in a fast-paced environment.
  • 2+ years of project management / project documentation coordination experience.
  • 2+ years’ experience in construction or design engineering coordination position is preferred.
  • Experience in working with remote teams is preferred.
  • Self-starter with excellent time management and organizational skills with proactive approach that is results-focused.
  • Demonstrated ability to work in a team-oriented, collaborative environment.
  • Demonstrated ability to communicate clearly and professionally, both verbally and in writing.
  • Advanced knowledge and experience using and maintaining electronic document management systems.
  • Strong administrative technical skills using MS Word, Excel, PowerPoint, Corporate Time Calendar required.
  • Demonstrated effective time management and organizational skills.
  • Demonstrated change management skills, as well as versatility in responding to change.
  • Demonstrated project coordination and workflow management skills.
  • Demonstrates a sense of urgency and proactive approach that is results-focused.
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Mon, 13 Aug 2018 00:00:00 PDT 0
<![CDATA[Study Start-Up Specialist I]]> Bayside Solutions is seeking Study Start-Up Specialist I to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Study Start-Up Specialist I:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Coordinates, guides and assists with all start up activities prior to site activation
  • Review, analyze and collate metrics to ensure processes are in place that drive efficiency and reduction of timelines across start up and contracts negotiation 
  • Ensures all start up information & requirements are kept up to date in a central repository for project teams 
  • Assists with label preparation and approval (local label representative) for studies in collaboration with local regulatory department 
  • Tracks metrics and study start-up timelines to identify trends and opportunities for improvement
  • Ensure adherence and compliance with local regulatory requirements and associated documentation

Required Qualifications:
  • University Degree preferably in a medical/science-related field
  • Prior work experience demonstrating knowledge and understanding of clinical trials, such as that obtained in a clinical trial monitor capacity, and experience managing projects
  • Demonstrated knowledge and understanding of ICH-GCP, the regulatory, ethics and contractual requirements for starting clinical trials in relevant country
  • Demonstrated competence in analysis, planning and problem solving.
  • Excellent communications skills including the ability to state opinions clearly, ask questions, seek clarification, communicate facts objectively, challenge when appropriate, and pursue issues to resolution
  • Ability to present clear messages from complex information/data to all levels in the organization in both written and spoken English
  • Experience working as part of a team with a proven ability to make an active contribution to the team' s performance and teamwork
  • Able to make effective decisions, self-motivated, assertive, and displays initiative
  • Proven project management and organizational skills and the ability to prioritize and manage multiple tasks with flexibility
  • Demonstrated computer literacy, usage of MS Office software, web-based systems and databases
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Fri, 10 Aug 2018 00:00:00 PDT 0
<![CDATA[Post Doc Fellow]]> Bayside Solutions is seeking a Post Doc Fellow to be part of our client’ s team in the Fremont area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Post Doc Fellow:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Develop mass spectrometry (MS) methods to support process development
  • Carry detailed characterization of proteins using HPLCMS including but not limited to, host cell protein analyses, sequence variant analysis, and quantitative proteomics analysis
  • Provide guidance to the project team with MS knowledges to review experimental protocols, results and reports from the external collaborators
  • Execute protein analytical work in a fast pace environment
  • Perform data analysis and interpretation, and making internal technical presentations
  • Participate project meeting with leading discussion for MS topics
  • Work in a highly interdisciplinary and collaborative environment as part of the Process Science team

Summary of Qualifications:
  • PhD with 0+ year’ s industry experience in protein analytics
  • Extensive experience with MS with 5+ years’ experience
  • Hands-on experience in protein analytics, with experience in 1 or 2 of the above described analytical assays
  • Good written and oral communication skills
  • Ability to work in a team environment

 

 
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Fri, 10 Aug 2018 00:00:00 PDT 0
<![CDATA[Sr. Maintenance Technician:]]> Bayside Solutions is seeking a Sr. Maintenance Technician to be part of our client’ s team in the Fremont area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Sr. Maintenance Technician:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Performs maintenance on site equipment and systems according to detailed work instructions, including some unique and highly complex assets such as autoclaves, Parts washers, WFI, fermentation vessels, Chromo Columns, Liquid handling modules, and tangential flow filtration skids, Records results in Enterprise
  • Identifies out-of-scope conditions and perform corrective actions Communicates results as required by SOP and lead identification of root cause and remediation of failures
  • Maintains equipment by providing troubleshooting to ensure equipment performance is reliable and meets expectations
  • Performs preventive, corrective, or emergency work orders and respond to service calls while the plant is in operation, which may include off-shift periods and weekends
  • Corrective work may include replacing electrical or powered component, including multiple phase motors
  • Assists in the troubleshooting to better understand deviations from proper operation 
  • Maintains and ensures documentation, both written and electronic, is accurate, complete and factual as required by policies, procedures, and regulatory guidelines
  • Documents activities supporting maintenance best practices to ensure that continuous improvement activities have adequate and reliable data for analysis
  • Ensures equipment/system documentation requirements are completely and properly documented in the Enterprise Asset Management System (EAM)
  •   Reviews and provides final approval (closing) on technician work orders
  • Develops or guides the development of metrics and information to be used in root cause analysis (RCA) meetings
  • Reviews and analyzes data collected by self or others in order to ensure proper documentation and adherence to procedures
  • Reviews updated or modified SOP' s and job plans procedures developed by other Technicians or contractors

Summary of Qualifications:
  • High School Diploma  or GED
  • Understanding of equipment start-up and project support.
  • Working knowledge of schematics, P&ID drawings, and ISA symbols & numbering                                                                   
  • Demonstrated ability to effectively maintain, troubleshoot and repair mechanical systems and equipment               
  • Requires a strong electrical, mechanical and technical aptitude
  • Ability and willingness to maintain accurate records
  • Attention to detail, safety, quality and customer requirements
  • Demonstrate a high level of personal motivation and initiative
  • Ability to adapt and be flexible with daily work assignment changes as well as a continuously improving work environment
  • Ability to make decisions within the scope of operating policies and procedures

 

 
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Fri, 10 Aug 2018 00:00:00 PDT 0
<![CDATA[BioRepository Technician]]> Bayside Solutions is seeking a  BioRepository Technician to be part of our client’ s team in the East Bay Area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

BioRepository Technician:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Performs BioRepository Management duties for BioSpecimen Management, with meticulous attention to details.
  • Works independently to receive shipments of human biological samples, verify sample integrity and data accuracy, process (centrifuge, aliquot, and pool) samples, consolidate inventory, retrieve and distribute samples, ship specimen collection supplies to partners, and monitor laboratory supply inventory.
  • Follows departmental work instructions, SOP’ s, OSHA safety regulations and GLPs to perform assigned tasks.
  • Duties include handling hazardous biological materials (BSL-2) as described above.
  • Works independently in a validated Laboratory Information Management System (LIMS), maintaining documentation in accordance with established procedures; performs basic database queries and creates new requests as needed.
  • Maintains a high level of organization to independently manage all aspects of complex service requests and thinks creatively to resolve challenges as encountered.
  • Works independently to communicate with diverse stakeholders, internal and external to Roche, regarding biological material shipments, schedules and discrepancies identified during the verification process.
  • Participates in laboratory certification and accreditation management activities, audit preparation, and team member recruitment activities.
  • Participates in required training related to position; takes personal responsibility for being current in all training activities.
  • Manages daily activities/responsibilities and assignments to meet business needs; establishes priorities using inputs from business requirements and/or internal customer needs.

Summary of Qualifications:
  • HS diploma or GED required; some undergraduate biological science coursework or Certificate (e.g. Lab Tech, EMT, LPN) preferred.
  • At least 6 months of handling human biological samples required.
  • Requires work with dry ice, -80 degree freezers, and human biological samples.
  • Ability to lift objects up to 30 lbs.
  • Good organizational skills are essential
  • Must be detail-oriented.
  • Results and goal-oriented.
  • Good written and verbal communication skills; able to read, write and speak English.
  • Ability to work in a fast paced and dynamic environment with efficiency; capable of handling multiple projects.
  • Good interpersonal skills and the ability to consistently project a positive and professional attitude.
  • Passionate about the importance of biorepository management.
  • Proficient in using e-mail and a basic knowledge and willingness to perfect understanding of Microsoft Word and Excel.
  • Must be a self-starter with a strong work ethic and adaptability.
  • Ability to work independently and as a team member.

 
]]>
Thu, 09 Aug 2018 00:00:00 PDT 0
<![CDATA[Project Manager IV]]> Bayside Solutions is seeking Project Manager IV to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Project Manager IV:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Ensure improvement methodology and tools are utilized effectively to maximize benefits
  • Deliver project goals on budget and on schedule
  • Develop conceptual customer needs into an approved project charter
  • Analyze business, process and systems performance, and identify improvement opportunities
  • Develop, evaluate and manage business case and cost/benefit analyses
  • Provide decision support and recommendations to select best options Communicate proactively with stakeholders and senior management regarding progress, issues and plans for resolution
  • Develop and use project plans to coordinate participants and track and report progress
  • Leverage industry research and analysis; serve as advocate & role model for integrating best practices into the organization
  • Operate with a high degree of autonomy and professionalism; successfully prioritize workload in accordance with business goals

Required Qualifications:
  • BS/BA (Engineering/Science preferred). Minimum 7 years of related analytical and business experience working in a complex
  • Minimum 3 years Project Management experience. Experience with implementation of process improvement initiatives
  • Ability to influence with or without authority, facilitate groups with diverse perspectives, bring teams to consensus/alignment
  • Takes accountability for actions, drives results, and learns from mistakes
  • Makes quality decisions and resolved problems rapidly
  • Ability to communicate effectively up and down, at all levels of the organization, teach and present complex and/or new ideas with clarity and simplicity
  • Excellent planning and prioritization skills with the ability to multitask and adapt
  • Able to synthesize large amount of information
  • Ability to define problem statement clearly and accurately and apply structured and disciplined methodology to identify data-driven root causes
  • Innovative and effective in solution development, risk mitigation, and execution
]]>
Thu, 09 Aug 2018 00:00:00 PDT 0
<![CDATA[Call Center Representative]]> Bayside Solutions is seeking a Call Center Representative to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world’ s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Call Center Representative -  Case Manager

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life-threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Provides customer focused reimbursement support to patients, pharmacists, physicians and internal sales force.
  • Educates, informs, and assists patients and providers to navigate through the reimbursement process for the assigned product.
  • Identifies barriers to reimbursement and continually identifies and recommends program efficiencies to the Supervisor to promote high quality of work by Access Solutions/GATCF staff.
  • Identifies and facilitates referrals to alternative coverage options and financial assistance programs for patients who are underinsured or require copy assistance.
  • Establishes relationships with appropriate stakeholders including internal & external partners.
  • May conduct necessary benefits, coverage and payer research/investigations to ensure appropriate resources, compliance with payer appeal policies, practices, timelines.
  • Educates, informs and generally assists patients and their families, as well as other related external or internal parties on how to navigate the appeals process.
  • This position may require some travel and flexibility in work shift
  • Periodic mandatory overtime throughout the year is required. This may include, but is not limited to, high referral season, new product or system launches, enrollment renewals, new line extensions, or any unexpected surge in volume or backlog situations.
  • Workdays are M-F, but may include weekends as needed.

Summary of Qualifications:
  • High school diploma or AA with five years of working experience is acceptable.
  • Bachelor’ s degree is highly preferred with one to two years of experience.
  • A minimum of 1-2 years of data entry is preferred.
  • Proficient in all aspects of reimbursement (i.e., benefit investigations, payer reimbursement policies, regulatory and administrative rules).
  • Demonstrates effective problem-solving skills and provides excellent customer service.
  • Excellent investigational and analytical skills with a proven ability to communicate effectively in both written and verbal format.
  • Ability to work collaboratively in a team structure and responsibly delegates next steps to appropriate team members.
  • Must be able to work in a fast paced environment, multitask, and maintain attention to detail.
  • Must have a reliable mode of transportation.
  • Must be able to work effectively under pressure and prioritize tasks.
  • Must be able to follow written Standard Operating Procedure.
  • Recommended experience with Mac operating systems.
]]>
Thu, 09 Aug 2018 00:00:00 PDT 0
<![CDATA[Scientist I]]> Bayside Solutions is seeking a Scientist I to be part of our client’ s team in the Fremont area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Scientist I:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Execute cell culture process development and optimization experiments using various vessels such as shake flasks, Wave and bench scale bioreactors, stainless steel and single use pilot scale bioreactors for the production of monoclonal antibodies and other recombinant proteins.
  • Monitor and evaluate mammalian cell culture performance in experiments utilizing various instruments such as cell counters, blood gas and chemistry analyzers, and others.
  • Prepare stock solutions and media for mammalian cell culture as needed.
  • Perform other lab support activities such as basic equipment maintenance, troubleshooting and lab organization.
  • Communicate own work effectively.
  • Occasional weekend work determined by project and experiment demand.

  Summary of Qualifications:
  • BS with 0-2 years’ experience in biochemical engineering, bioengineering, chemical engineering, biotechnology, life sciences, or related fields.
  • Fundamental understanding of biochemistry, cell biology, biotechnology, or chemical engineering.
  • Hands on experience with aseptic techniques is a must.
  • Mammalian cell culture lab experience strongly desired.
  • Experience in Microsoft Office tools including Word, Excel, and PowerPoint is a must; Experience in experiment design and data analysis using statistical tools and software is a plus.
  • Experience working in GMP and on harvest process is also a plus.

 

 

 
]]>
Thu, 09 Aug 2018 00:00:00 PDT 0
<![CDATA[Biosample Research Scientist]]> Bayside Solutions is seeking a Biosample  Research Scientist to be part of our client’ s team in South San Francisco. This is an opportunity to work with a great Biotechnology company focused on the discovery and development of therapies for patients with neurodegenerative diseases, including Alzheimer’ s disease, Parkinson’ s disease, ALS and others.

Our client was founded by scientists, industry experts and investors who share the vision that recent scientific insights into the genetic causes and biological processes underlying neurodegenerative disease, together with new translational medicine tools, offer an unprecedented opportunity to discover and develop effective medicines. Denali is rigorously pursuing a science-driven approach to translational medicine and clinical development.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Biomarker Research Scientist

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Isolate white blood cells / PBMCs from human blood by rigorously following a standardized procedure
  • Organize and maintain a sample biorepository, including accessioning samples in an electronic database, labeling / barcoding, and reconciling with physical cold chain storage
  • Participate in migration to Laboratory Information Management System (LIMS)

Required Qualifications:
  • Willing to work some Saturdays and evening hours with minimum 24 hours advance notice of timing
  • BS/MS with at least 2 years of academic or industry laboratory experience
  • Experience working with human whole blood including isolation of PBMCs
  • High attention to detail and organizational skills
  • Strong written and oral communication skills
  • General computer skills (including Excel)
  • Ability to multi-task, ask questions, and excel in a dynamic work environment

 
]]>
Wed, 08 Aug 2018 00:00:00 PDT 0
<![CDATA[Manufacturing Bioprocess Technician]]> Bayside Solutions is seeking a Manufacturing Bioprocess Technician to be part of our client’ s team in the Vacaville. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Manufacturing Bioprocess Technician:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Support the Manufacturing department by working effectively to meet department goals, objectives and tasks to achieve desired results.
  • Responsible for completing assigned tasks which include cleaning, sterilizing, and prepping parts used in the manufacturing environment.
  • Provides timely and accurate verbal and written communications of processing updates, discrepant events, and scheduling delays.
  • Work with senior technicians and leads to prioritize tasks and assignments and make recommendations to maximize efficiency and productivity based on shift needs.
  • May also include stocking, inventory and environmental monitoring.

Summary of Qualifications:
  • Bachelor' s Degree in Life Sciences or Engineering, or equivalent education with a minimum of 2 years of work experience will be considered as well.
  • Must possess solid  problem solving, interpersonal communication, and team-based skills.
  • Demonstrated experience and knowledge of working in a GMP environment compliantly and safely.
  • General skills:   working with pressurized systems / high temperatures / acidic & basic solutions, follow Standard Operating Procedures (SOPs), making manual connections.
  • Specific skills:   chromatography/TFF/UFDF processing, preparing buffer/media solutions, chromatography column packing, SAP, Trackwise.
  • Must be a self-starter with strong focus on quality, details, results and application of cGMP.
  • Must be able to work weekends and off shift.

 
]]>
Wed, 08 Aug 2018 00:00:00 PDT 0
<![CDATA[Research Associate]]> Bayside Solutions is seeking an Research Associate to be part of our client’ s team in South San Francisco. This is an opportunity to work with a great Biotechnology company focused on the discovery and development of therapies for patients with neurodegenerative diseases, including Alzheimer’ s disease, Parkinson’ s disease, ALS and others.

Our client was founded by scientists, industry experts and investors who share the vision that recent scientific insights into the genetic causes and biological processes underlying neurodegenerative disease, together with new translational medicine tools, offer an unprecedented opportunity to discover and develop effective medicines. They are rigorously pursuing a science-driven approach to translational medicine and clinical development.

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research  Associate

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Handling rodents.
  • Observation and reporting of animal health, cage change outs, assembling clean cages or preparing cage components for disposal/recycling.
  • Cleaning vivarium holding rooms and associated storage spaces.
  • Keeping inventory and restocking of vivarium supplies, biohazard disposal, record keeping, and general housekeeping.

Required Qualifications:
  • Previous work in an animal facility is necessary with at least 2 years of experience. 
  • Knowledge of disposable caging systems, blood collection, measurements of body weights, and data capturing software is desirable. 
  • Strong verbal and written communication skills are required. 
  • Must be able to lift 50lbs in order to perform routine lifting and loading/unloading of supplies. 
  • Must also be able to work independently and with little supervision. 
  • Position may require occasional weekend health checks. 
  • AALAS certification strongly preferred but not required.

 
]]>
Wed, 08 Aug 2018 00:00:00 PDT 0
<![CDATA[Quality Control Analyst]]> Bayside Solutions is seeking a Quality Control Analyst to be part of our Client’ s team in the Peninsula. This is an opportunity to work with a molecular diagnostics company that engages in the detection and monitoring of life threatening viral diseases in the areas of cervical cancer, HIV/AIDS, hepatitis, breast and ovarian cancer, and organ transplant rejection.

The company also provides personalizing HIV testing; HPV OncoTect; incellCount CD4/CD8 reagent, which is intended for flow cytometry based analysis in lysed human whole blood samples; fixation/permeabilization products; and hybridization core reagents, including fixation permeabilization solutions, phosphate buffered saline, buffers for hybridization, and sodium citrate solutions.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Quality Control Analyst

Job Benefits:
  • An opportunity to join a company focused on the development and delivery of novel, targeted drugs for treating a variety of therapeutic areas.
  • Work for a company that is local to the bay area, in the beautiful South San Francisco area.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Receive and inspect production materials, perform functional testing, and document conformance to specifications.
  • Perform hands-on laboratory testing for product incoming quality control of reagents.
  • Trend QC and product performance results.
  • Design and perform stability studies to verify product shelf life; write study reports to summarize results.
  • Conduct technical studies to support Quality Control and Manufacturing documents.
  • Perform internal manufacturing procedures e.g. product labeling and assembly.
  • Assist with Design Transfer documentation for the Design History File of new products.
  • Write non conformance reports and corrective and preventive actions reports as needed.
  • Perform monthly inventory of products for accounting.
  • Assist in offsite storage facility management.
  • Act as a back-up for shipping related activities.

Required Qualifications:
  • BS in Biochemistry, Molecular Cell Biology or related field.
  • Minimum of 1 year of Quality Control experience in a scientific industry.
  • Good understanding of FDA QSR (cGMP) and ISO 13485, 9001.
  • Laboratory experience. Proficient in using basic lab equipment (micro-pipettors, microcentrifuge, cell analyzer).
  • Knowledge and experience in GMP, GDP, GLP.
  • Effective computer skills, especially proficient in Excel and Word. 
  • Effective problem solving, troubleshooting and analytical skills.
  • Flow cytometry experience is a plus.
]]>
Wed, 08 Aug 2018 00:00:00 PDT 0
<![CDATA[Manufacturing Associate I]]> Bayside Solutions is seeking a Manufacturing Associate I to be part of our client’ s team in the Fremont area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Manufacturing Associate I:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Prepare a variety of media and stock solutions that are transferred from tank to bag or tank to tank in order to support cell culture main operations to facilitate proper cellular growth per SOP
  • Able to follow SOP’ s to perform routine cleaning activities of parts and equipment using manual cleaning methods, designated parts washers, Clean-In-Place (CIP) and COP(Clean-Out-Of-Place) systems. As well as collecting rinse water samples and performing swabs on required equipment for testing
  • Execute proper documentation and measures to initiate changing over of parts and equipment to be released for use
  • Performs a majority of operations in a cGMP clean room environment.
  • Practices ergonomic safety and use appropriate personal protective equipment (PPE) in all operations
  • Documents execution of operations through the Bio Manufacturing Execution System (BioMES), batch record and equipment use logbook using Good Documentation Practices (GDP). Interchanging between electronic and paper documentation procedures
  • Performs internal support duties including stocking consumables/materials, updating controlled SOP binders, appropriately discarding expired reagents, recognizing and reporting process and equipment anomalies
  • Reports any issues related to manufacturing performance, process and safety to the team lead or Manager in order to ensure safety and compliance with regulations and cGMPs and to facilitate continuous process improvement
  • Participates in training and development opportunities in order to gain an understanding of SOPs,
  • Performs routine housekeeping of the manufacturing plant using the 5S organization methodology by using appropriate equipment safety signage, labeling of parts-in-process, sweeping water pools to the floor drain, and picking up parts from the floor
  • Collaborates within team and department in order to follow best practices and meet department goals

  Summary of Qualifications:
  • Requires a High School Diploma or equivalent plus four (4) years closely related technical experience, preferably in a pharmaceutical or chemicals manufacturing environment
  • An Associates Degree with a minimum of two (2) years closely related technical experience, preferably in a pharmaceutical or chemicals manufacturing environment; or a Bachelors’ degree, preferably in a science or engineering field is preferred with 1+ years of GMP exp
  • Experience working with established GMP procedures and bulk manufacturing
  • Technical knowledge of manufacturing systems, methods and procedures Understanding of cell culture processes
  • Possess effective troubleshooting skills with equipment
  • Demonstrated ability to be organized and work well in small work groups
  • Demonstrated mathematical skills, including the ability to perform addition, subtraction, multiplication, division, and conversions
  • Detail oriented
  • Experiences in related biotechnology/pharmaceutical industry strongly preferred
  • Must be able to learn and perform basic computer operations such as MS Office and Outlook and other computer based software
  • Preferred skills include experience in: Mammalian cell culture, Bio Manufacturing, Execution System (BioMES), Process Control System DeltaV, Laboratory Management Information System (LIMS)

 

 

 
]]>
Wed, 08 Aug 2018 00:00:00 PDT 0
<![CDATA[Project Manager I]]> Bayside Solutions is seeking a Project Manager I to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Project Manager I:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Develops and maintains a system to track EDIS-related resourcing data across Pharma R&D, including gathering current resource information, tracking changes, and escalating issues with resource allocation to the EDIS leadership
  • Supports EDIS leadership in annual budget planning and develops and maintains a system to track EDIS-related spend across the project portfolio throughout the year
  • Supports project-related activities and milestone tracking to help maintain a high-quality, accurate, and transparent EDIS portfolio plan
  • Supports in the preparation, execution, and follow up for EDIS leadership team meetings and presentations, including presentations, agenda planning, minutes, and action-item tracking as needed
  • Understands and represents EDIS objectives and values within the Program and across the Roche group
  • Partner closely with EDIS data standards work stream lead, to coordinate all EDIS data standards related activities, including but not limited to:
  • Setting agenda and arranging speakers during weekly calls.
  • Liaising with other EDIS project teams on an on-going basis to help ensure a strong partnership with data standards work stream participants is fostered and maintained.
  • Maintain an EDIS data standards roadmap, and help to ensure all key milestones and deliverables are achieved.
  • Coordinate all aspects associated with annual global F2F workshop for EDIS work stream participants, including logistics, agenda, and team-building activities.

Qualifications:
  • Minimum: BS/MS or equivalent, with 3+ years of related experience in a fast-paced, project-based environment, pharma or biotech experience preferred
  • Strong project management skills, including roadmap development, resource/budget tracking, and meeting planning
  • Experience working in a global, multi-cultural, cross-functional environment
  • Excellent interpersonal skills with the ability to develop important relationships with customers and key stakeholders
  • Results and detail-oriented
  • Facility with MS Project tools (word, excel, PPT, etc.) a must
  • Ability to work with various levels within the organization and to collaborate within a complex, dynamic environment, handling multiple tasks and priorities
  • Ability to identify issues that could impact timely completion of group activities, and develop strategies and provide recommendations to address problems
  • Self-motivated and able to deal successfully with ambiguity
  • Ability to travel internationally as required
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Wed, 08 Aug 2018 00:00:00 PDT 0
<![CDATA[Maintenance Mechanic II]]> Bayside Solutions is seeking a Maintenance Mechanic II to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Maintenance Mechanic II:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Responsible for the motor, pump and valve maintenance for specific fermentation and purification equipment
  • Experience with the maintenance of production equipment, rather than Operational experience
  • Maintenance, repair, fault diagnosis and troubleshooting of manufacturing process equipment, support equipment, utility equipment and systems, and HVAC/R equipment and systems
  • Timely completion of tasks and workorders with appropriate documentation according to standard operating procedures, applicable standards, guidelines, practices, and policies
  • Safe operation of tools and shop equipment, and safe execution of work in the field
  • Confined Space Entry in accordance with all applicable laws, regulations, and policies
  • Knowledge of cGMP, good documentation practices, and able to follow Standard Operating Procedures (SOP' s)
  • Basic computer and data entry skills
  • Ability to read and understand Piping and Instrumentation Drawings
  • Able to work off hours up to 12hrs shifts
  • Able to lift at least 35lbs

Qualifications:
  • High School Diploma or GED
  • Minimum of two years’ experience in an industrial maintenance or operation environment is required
  • Documented completion of technical or trade courses is a plus. -Bio-Tech  or pharmaceutical experience
  • Working knowledge of various pumps, mechanical seals, motors, and laboratory equipment (such as autoclaves and washers)
  • Ability to safely operate shop equipment
  • Confined Space Entry capable and willing in accordance with all applicable laws, regulations, and policies
  • Ability to read and understand Piping and Instrumentation Drawings
  • Ability to complete tasks by following Standard Operating Procedures
  • Basic computer skills, with the ability to utilize programs such as Microsoft Word and Excel, as well as email

 
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Wed, 08 Aug 2018 00:00:00 PDT 0
<![CDATA[Research Associate I]]> Bayside Solutions is seeking a Research Associate I to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate I:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Develop and routinely employ bioanalytical methods for the quantitative and qualitative analysis of new chemical entities and their metabolites in plasma, tissues, and other
    biological matrices.
  • Interpret and provide bioanalytical results to project teams in support of drug discovery and development.
  • Work as a member of the bioanalytical group and will be responsible for sample preparation, tissue homogenization, sample extraction techniques (e.g. LLE, SPE, and PP), data acquisition on a triple-quadrupole platform (Sciex API5500, etc), and data processing using Analyst and Watson-LIMS.

Summary of Qualifications:
  • BS or MS in a relevant scientific discipline chemistry, biochemistry, etc with typical relevant experience of 0-3 years.
  • Proven ability to independently design and  execute experiments by LC-MS/MS in support of drug discovery and early development programs in a fast-paced environment.
  • Good understanding of preclinical ADME and bioanalytical techniques.
  • Ability to assist in troubleshooting when instrument or assay problems arise.
  • Responsibilities will include basic bioanalytical research, electronic laboratory notebook keeping and communication of results to project teams.
  • Experience with independent operation of various LC-MS platforms and automated liquid handlers is preferred.
  • Possess excellent oral and written communication skills.
]]>
Tue, 07 Aug 2018 00:00:00 PDT 0
<![CDATA[Lab Tech Ops]]> Bayside Solutions is seeking a  Lab Tech Ops to be part of our client’ s team in the East Bay Area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.
 

You can find additional information on our company website at www.baysidesolutions.com

Lab Tech Ops:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Performs labeling and kit assembly operations consistent with quality standards
  • Follows all department work instructions and safety regulations and executes all manufacturing activities in accordance with cGMP/cGDP/cGLP guidelines
  • Visually inspects products for defects and conformance to quality standards
  • Completes necessary packaging documentation (production manufacturing records) and associated SAP transactions to ensure all components meet requirements pertaining to lot numbers, expiration dates, intermediates, reconciliation, etc
  • Cleans work area and decontaminates work surfaces in accordance with defined procedures and performs duties in accordance with all safety regulatory requirements
  • Performs general/routine maintenance/upkeep of the packaging area and packaging lines
  • Performs material handling activities according to defined procedures, which includes picking, issuing, stock transfer and receipt transactions.

Summary of Qualifications:
  • High school diploma or Associates Degree in a related field 
  • 1-3 years manufacturing experience, preferably with labeling and packaging experience in the pharmaceutical or medical device industry

 
]]>
Tue, 07 Aug 2018 00:00:00 PDT 0
<![CDATA[Analytical Development, Sr. Associate/Scientist I]]> Bayside Solutions is seeking an Analytical Development, Sr. Associate/Scientist I to be a part of our partner’ s team in the Newark  area. This is an opportunity to work within a life-changing biotechnology company poised to change the neuromodulator aesthetic and therapeutic product categories.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

 

Analytical Development, Sr. Associate/Scientist I Job Benefits:

Job Benefits:
  • An opportunity to join a bio-technology company developing and delivering next-generation neuromodulator, daxibotulinumtoxinA, and highly purified botulinum toxin  type  A.
  • Work for a company that likes to dream and think big! They are local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Regularly apply basic theory and principles from one’ s technical expertise to develop, optimize, and transfer analytical assays for product characterization, lot release, and stability testing.
  • Coordinate and conduct routine testing support for other groups within  Development and Manufacturing Functions.
  • Perform routine instrument/equipment maintenance and calibration checks to ensure the proper function and compliant use.
  • Provide regular progress updates to manager and present data to internal and external audiences in a succinct and well organized manner.
  • Author test methods and development reports.
  • Serve as subject matter expert for at least one technical area and train other laboratory personnel on the use and maintenance of equipment.
  • Lead technical transfer of assays to and from contract test laboratories or to QC.
  • Plan experiments with limited manager oversight and work independently to achieve deliverables with minimal instruction.
  • Develop and implement laboratory policies for critical reagents, data management, organizational performance, and continuous improvement.
  • Maintain laboratory notebooks and forms consistent with Good Documentation Practices.
  • Maintain adequate supplies of laboratory reagents and coordinate biohazard and chemical waste disposal.

Required Qualifications:
  • Chemistry or Biological Science degree:  bachelors with 8+ years, masters with 6+ years, or doctorate with 2+ years of experience in biopharmaceutical analytical development.
  • Solid training in general laboratory practices (e.g., buffer preparation, sample dilution, micro-pipetting).
  • Experience in the development and optimization of assays for pharmaceutical characterization.
  • Experience in one or more of the following areas, including training and troubleshooting experience: o Chromatography or capillary electrophoresis o Mass spectrometry o Immunochemical assays o Spectroscopy o Cell based assays
  • Working knowledge of cGMP practices and ICH guidelines.
  • Excellent planning and organizational skills with good documentation, record management habits, and attention to detail.
  • Proficient with Microsoft-based applications (Word, Excel, PowerPoint, Outlook)

 
]]>
Mon, 06 Aug 2018 00:00:00 PDT 0
<![CDATA[Administrative Associate 4]]> Bayside Solutions is seeking an Administrative Associate 4 to be part of our client’ s team. This is an opportunity to work with a private research university in the South Bay, California.  This Client is known for its academic strength, wealth, proximity to Silicon Valley, and ranking as one of the world' s top-ten universities

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Administrative Associate 4

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life-threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Advanced computer skills and demonstrated experience with office software and email applications. 
  • Demonstrated success in following through and completing projects. 
  • Excellent organizational skills and attention to detail. 
  • Strong verbal and written communication skills. 
  • Excellent customer service and interpersonal skills. 
  • Ability to prioritize, multi-task, and assign work to others. 
  • Ability to take initiative and ownership of projects. 
  • Ability to routinely and independently exercise sound judgment in making decisions. 

Summary of Qualifications:
  • Experience working in global programs and with global constituencies and visitors.
  • 4+ years’ experience as Administrative Assistant 
    Strong financial and expenses experience.
  • Pre- and post-award grants management experience.
  • Bachelor' s degree highly preferred.

 
]]>
Mon, 06 Aug 2018 00:00:00 PDT 0
<![CDATA[Production Support Manager]]> UAT Production Support Manager

Location: Austin, TX or Sunnyvale, CA

Principal Duties and Responsibilities include but are not limited to: 
  • Understanding and driving technical root cause analysis across multiple systems to ensure issues are resolved
  • Collaborate with different teams in the Company to improve operational process.
  • Provide support to Managers across Company for systems improvement changes and testing.
  • Accountable for developing metrics and reports on frequency of production issues relating to systems.
  • Identifying Issues related to System GAPS
  • Own the development training materials, process documentation and process improvement
  • Work closely with Multiple teams for successful execution of UAT Plan

Qualifications
  • Must have a Bachelor’ s Degree with 5 years of User Acceptance Testing experience
  • Experience working on multiple projects providing production support and participating in UAT (creation, execution and resolution of issues)
  • Experience with ERP and Supply Chain systems
  • Experience setting up an infrastructure of metrics to optimize issue resolution
  • Excellent analytical skills to investigate and drive issues found in UAT activities
  • Exceptional organization, documentation and presentation skills
]]>
Fri, 03 Aug 2018 00:00:00 PDT 0
<![CDATA[Pharmacology Associate II]]> Our client in Menlo Park is looking to have a Pharmacology Associate II join their growing team!

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Pharmacology Associate II

Job Benefits:
  • An opportunity to significantly impart the future of the company’ s operations
  • A competitive base salary
  • On the job training, both in person/online

Summary of Responsibilities:
  • Competent skills in laboratory animal science, work closely with the members of Preclinical Development to evaluate therapeutic candidates in animal models
  • Demonstrate proficiency in all commonly utilized rodent biomethods
  • Knowledge of laboratory animal health and welfare, as well as an understanding of Preclinical drug development processes, are essential

Required Qualifications:
  • The ideal candidate will possess a minimum of 3-5 years experience executing Preclinical in vivo studies.
  • Perform administrations via IP, IM, SC, IV, intravitreal and
  • Experience with animal model development, preferably ocular disease models
  • Ability to assist with the write-up of study protocols and reports
  • subretinal routes
  • Perform blood collection via submandibular, retro-orbital, and cardiocentesis routes
  • Perform necropsy and tissue collection for Non-GLP preclinical studies
  • Experience establishing, and maintaining, study sample inventories in a cross-functional team setting
  • Experience establishing, and maintaining, a laboratory supply inventory system; setting up vendor accounts, placing and receiving orders, tracking usage and anticipating supply needs
  • Proficiency in Microsoft Word, Excel, PowerPoint and GraphPad Prism
  • Understanding of program timelines, with emphasis on specific deliverables
  • Working knowledge of Gene Therapy, specifically AAV Vectors
  • Experience with ocular disease models; performing regular ocular examinations and imaging utilizing slit lamp, fundus microscope, optical coherence tomography (OCT), and electroretinography (ERG) ophthalmic equipment
  • Experience conducting tissue isolation, fixation, preparation of tissue sections, tissue staining including immunohistochemistry and ELISA-based assays
  • Must be willing to travel between Menlo Park, CA and the offsite Vivarium, located in Mountain View, CA
]]>
Fri, 03 Aug 2018 00:00:00 PDT 0
<![CDATA[Materials Specialist]]> Bayside Solutions is seeking a Materials Specialist to be part of our client’ s team in the South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Materials Specialist:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Responsible for the accurate receipt, verification, record keeping, distribution, and shipment of materials and goods.
  • Acceptance of incoming materials by ensuring paperwork is accurate and materials are received in good conditions.
  • Prepare receiving documents, route receiving information, prepare outgoing shipments, observe proper handling, storage and/or temperature requirements.
  • Provide for internal distribution of Good Manufacturing Practicesmaterials to company facilities.
  • Pack materials for proper shipping conditions.
  • Prepare shipping documents and manifests for hazardous materials.
  • Perform x-ray scanning of packages.
  • Process and receive radioactive materials, apply proper placards, perform campus pick-ups of outgoing shipments, and apply asset tags to capital equipment.
  • Maintain equipment and work areas for cleanliness.
  • Operate material handling equipment in a safe and appropriate manner.
  • Independently follows Current Good Manufacturing Practice procedures.
  • Clearly understands the importance of accurate GMP documentation.
  • Observe all health and safety guidelines.

Summary of Qualifications:
  • Adjust to schedule changes, work overtime as necessary and float between groups as needed to support operations.
  • Ensure that all work is completed by end of day.
  • Utilize time wisely to maximize productivity.
  • Serve as a liaison between customers and warehouse staff.
  • Proficient in Word, Excel, gDocs for data entry.
  • Communicate clearly, both verbally and in writing.
  • Meet timeline commitments and inform others of status, issues, and customer requests as necessary.
  • Adheres to appropriate laws, GNE regulations and programs, and documentation procedures.
  • Adhere to safety safety guidelines as required for your area.
  • Complete training records in a timely manner. Individual will be driving company vans and/or bobtail trucks.
  • Forklift certification is a plus.
  • Previous Experience with packaging and x-ray equipment.
  • Attention to detail.
  • Adherence to safety procedures.
  • Excellent communication skills; proficient in Word and Excel.
]]>
Thu, 02 Aug 2018 00:00:00 PDT 0
<![CDATA[Laboratory Animal Technician]]> Bayside Solutions is seeking a Laboratory Animal Technician to be a part of our Client’ s team in South San Francisco. This is a unique opportunity to join a growing team of business professionals focused on providing novel drugs to help significantly improve the lives of patients with various disorders and rare diseases. 

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com

Laboratory Animal Technician

Summary of Responsibilities:  
  • The primary responsibility for this position is to conduct PK experiments for small molecule drug discovery projects in laboratory animals
  • Dosing, sample collection and laboratory operations to process biological specimens.
  • Additional responsibilities will include study documentation, planning, and preparation of data collection forms.

Required Qualifications:  
  • Strong animal handling skills. Must be dedicated to providing humane animal care in accordance with all relevant regulations & current practice standards.
  • Ability to dose drugs to rats and mice by multiple delivery routes, including oral gavage, intravenous injection and intraperitoneal injection.
  • Blood collection from cannulated rats.
  • Blood collection from rats/mice by retro-orbital or tail vein bleeding or cardiac puncture.
  • Harvesting of different tissues/organs from mice and rats.
  • At least 3 years vivarium experience and familiarity with working within an animal research facility.
  • Must have good interpersonal and communications skills; able to work effectively with variety of people; high degree of professional integrity; strong work ethic.
  • LAT certification or equivalent is preferred
]]>
Thu, 02 Aug 2018 00:00:00 PDT 0
<![CDATA[Research Associate, BioAnalytical Testing I]]> Bayside Solutions is seeking a Research Associate, BioAnalytical Testing I to be part of our client’ s team in Marin County. This is an opportunity to work with one of the largest Biopharmaceutical companies in the world developing innovative medicine to improve the quality of patients’ lives.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate, BioAnalytical Testing I:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Perform quantitative and semi-quantitative assays on non-clinical and clinical samples such as but not limited to serum, plasma, and urine, including immunoassays (ELISA) for therapeutic protein concentration and antibodies to therapeutic proteins, enzymatic activity assays, and glycosaminoglycans determinations.
  • Assist in development and qualification of new test methods as needed to reach company milestones.
  • Prepare or revise SOPs and departmental forms, assay worksheets, deviation investigations and associated GLP documentation.
  • Ensure GLP-compliant sample handling, assay performance and laboratory operations through adherence to SOPs and departmental practices
  • Interact with Corporate Compliance regarding data auditing
  •   Participate in internal and external inspections and audits

Required Qualifications:
  • Bachelor’ s degree or equivalent experience with clinical assays or other quantitative analytical methods in a biological or biochemical field.
  • Required: At least 2 years of experience in a bioanalytical laboratory, research laboratory, or biotechnology company performing bioanalytical assays.
  • Skills with ELISA and other analytical methods in a GLP-compliant environment, or equivalent analytical experience in a regulated lab environment
  • Experience with GLP or GMP documentation and testing.
  • Excellent writing and verbal communications skills.
]]>
Thu, 02 Aug 2018 00:00:00 PDT 0
<![CDATA[Process Scientist I]]> Bayside Solutions is seeking a Process Scientist I to be part of our client’ s team in the Fremont area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Process Scientist I:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Execute cell culture process development and optimization experiments using various vessels such as shake flasks, Wave and bench scale bioreactors, stainless steel and single use pilot scale bioreactors for the production of monoclonal antibodies and other recombinant proteins. Monitor and evaluate mammalian cell culture performance in experiments utilizing various instruments such as cell counters, blood gas and chemistry analyzers, and others.
  • Prepare stock solutions and media for mammalian cell culture as needed.
  • Perform other lab support activities such as basic equipment maintenance, troubleshooting and lab organization.
  • Communicate own work effectively.
  • Occasional weekend work determined by project and experiment demand

  Summary of Qualifications:
  • BS with 0-2 years’ experience in biochemical engineering, bioengineering, chemical engineering, biotechnology, life sciences, or related fields.
  • Fundamental understanding of biochemistry, cell biology, biotechnology, or chemical engineering.
  • Hands on experience with aseptic techniques is a must.
  • Mammalian cell culture lab experience strongly desired.
  • Strong communication and organization skills; be able to multi-task; be highly self-motivated, flexible, be able to collaborate and work effectively in teams.
  • Experience in Microsoft Office tools including Word, Excel, and PowerPoint is a must; Experience in experiment design and data analysis using statistical tools and software is a plus.
  • Experience working in GMP and on harvest process is also a plus.
]]>
Thu, 02 Aug 2018 00:00:00 PDT 0
<![CDATA[Senior Mechanical Engineer]]> Bayside Solutions is seeking a Senior Mechanical Engineer to be a part of our partner’ s team in the San Francisco East Bay Area. This is an opportunity to work with a Biotechnology company focused on providing fast acting therapeutic relief through a proprietary transdermal system.

Our partner’ s culture is fosters creativity, execution, accountability, urgency, and transparency. These are aspects of that are essential for establishing a robust portfolio of products that they have in development.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Job Benefits:
  • An opportunity to join a patient-focused organization aimed at developing existing therapeutics to be applied to their drug delivery system.
  • Work for a company that is local to the bay area and recognized as a leader of innovation
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K

Summary of Responsibilities:
  • Develops new components and device configurations. Makes improvements to the existing device design
  • Provides guidance and oversees the manufacturing processes for device components and assembly at CMO’ s
  • Prepares and executes feasibility studies on new components.
  • Conducts design reviews and follows device design control requirements during development and implementation of new designs
  • Leads all Solid Works design activities
  • Provides administrator role for CAD files in Solid Works PDM

Required Qualifications:
  • B.S. in Mechanical Engineering
  • 7+ years’ experience designing equipment preferably in a GMP environment
  • Previous medical device or pharmaceutical experience
  • Familiarity with design control fundamentals
  • Excellent interpersonal skills to allow effective participation in project teams.
  • Self-motivated person with initiative to complete tasks independently.
  • Excellent oral and written communication skills.
  • Experience with injection molding part design and manufacture
  • Experience in equipment validation
  • Experience designing and drafting with Solid Works
  • Experience using Solid Works PDM or similar
  • Desire to work in a hands-on environment
  • The candidate must be a detail-oriented, fast troubleshooter and bring a positive, open minded attitude with a willingness to learn.
  • Willingness to work in a clean room environment and interface with manufacturing personnel.

 
]]>
Thu, 02 Aug 2018 00:00:00 PDT 0
<![CDATA[Sr. Research Associate, Process Development]]> Our client in Menlo Park is looking to have a Sr. Research Associate, Process Development join their growing team!

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Sr. Research Associate, Process Development

Job Benefits:
  • An opportunity to significantly impart the future of the company’ s operations
  • A competitive base salary
  • On the job training, both in person/online

Summary of Responsibilities:
  • Help with manufacturing of AAV through the downstream purification process (cell lysate to final formulation)
  • Streamline current processes
  • Work hands-on to develop, optimize, and scale-up downstream processes for the purification of AAV vectors from small to large scale purification systems in a laboratory setting
  • Design and execute experiments following appropriate laboratory procedures and produce competent and reproducible results to a high technical standard
  • Appropriately analyze data, interpret results, and maintain accurate records with minimum supervision
  • Interact with Assay Development, QC, QA, and pre-clinical group
  • Develop novel AAV manufacturing processes with the highest quality according to corporate timelines in order to advance Adverum Biotech’ s product pipeline
  • Ensure a safe work place in compliance with the company and EH&S' rules and regulations
  • Keep current with advances in downstream processes for viral vector production

  Required Qualifications:
  • MS with 2-4 years of experience or BS with 4+ years of experience in Chemical Engineering, Biochemistry, Cell & Molecular Biology or related life science fields
  • Gene therapy viral vector production experience is required
  • Expertise in AAV or other gene therapy vector expression in mammalian cells via transient transfection is a plus
  • Hands-on experience with density-gradient ultracentrifugation is highly desirable
  • Experience with protein purification including hands on experience with TFF (Hollow Fiber / Cassettes) UF/DF, GE AKTA (Avant, Pilot), chromatography at small/pilot/large scale is a plus
  • Proficiency in general molecular biology techniques including ELISA, qPCR, BCA
  • Western Blot and Silver Stain experience is preferred but not required
  • Experience drafting SOPs, Batch records, reports, and protocols is preferred

 
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Wed, 01 Aug 2018 00:00:00 PDT 0
<![CDATA[HR Assistant]]> Bayside Solutions is seeking a HR Assistant to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

HR Assistant

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Upload and scan new hire documents as well as a variety of employee documents into the eFile database creating an electronic employee file
  •   Retrieve files from off-site storage facility as needed; purge I-9 documents on a monthly basis
  • Perform pre-hire functions weekly in Taleo and I-9 database
  • Assist at new hire orientation weekly
  • Review and prepare Proprietary Agreements for signature
  • Organize file room on a regular basis
  • Miscellaneous tasks and project work as needed

Qualifications:
  • SAP experience
  • Prior experience working in a Human Resources department (2 years) is preferred
  • General office/administrative experience
  • Computer skills (Word, Excel, Powerpoint,)
  • Experience with Workday, Taleo or another ATS is preferred as well as various databases
  • Also required are excellent analytical, documentation, and written/verbal communication skills
  • Deadlines are very important in this position and prioritization and time management experience is a must
  • The ideal candidate must have a proven track record of showing discretion and maintaining confidentiality
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Wed, 01 Aug 2018 00:00:00 PDT 0
<![CDATA[Quality Assurance Specialist]]> QA Engineer/Test Analyst-  Automation 

Financial Investments

San Mateo, CA

The QA Specialist works closely with business users and the project team to analyze business requirements in order to create project test scenarios and provide feedback on the actual system implementation of the business logic.   The QA Specialist will create test plans, test cases, and will participate in user acceptance testing to ensure that the highest quality products are released to production.

Responsibilities
  • Expert experience with one of the following (Test Complete, HP QTP, Silktest)
  • Writing and executing SQL scripting
  • Participate in business requirements documentation reviews to extract test scenarios
  • Work closely with Application Development Group to promote software quality standards
  • Coordinate with the Projects and Application Development teams to drive product quality
  • Work closely with the Projects Group to replicate customer issues and application use cases
  • Design, document and execute test procedures
  • Conduct test entry reviews and record and document test results
  • Investigate, recommend, implement and manage testing tools

 Qualification
  • 3+ year' s  experience testing software in a structured setting
  • Bachelor’ s degree or equivalent combination of experience and education
  • Experience testing Microsoft Dynamics solutions
  • Ability to define problems, collect data, establish facts, and draw valid conclusions
  • Broad experience designing and maintaining automated tests
  • Experience with standard software tools for test case management and defect tracking
  • In-depth knowledge of best practices for the Software Development Life Cycle

 
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Wed, 01 Aug 2018 00:00:00 PDT 0
<![CDATA[Research Project Manager]]> Bayside Solutions is seeking a  Research Project Manager to be part of our client’ s team in the East Bay Area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com

Research Project Manager:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Project leadership – takes responsibility for understanding at a basic level the business and scientific objectives of the sponsors and collaborators, and for coordinating all members of the team associated with a project
  • Project planning – documents at a high level the major objectives and milestones associated with a project, members of the project team and their roles and commitment level on the project, and works with scientific/technical team lead(s) to map out tasks and timelines to achieve the goals
  • Project communication – establishes and coordinates the events and methods associated with communicating project information
  • Project delivery – provides ongoing monitoring and documentation of objectives, priorities, resources, decision points, and sponsor satisfaction. Facitilates decision making as needed
  • Project administration – accounting activities associated with projects, including weekly or monthly reporting as needed

Summary of Qualifications:
  • Scientific research, particularly molecular biology and genomics or in digital pathology
  • Software design, development and support, preferably in image science algorithm software development
  • Project management, preferably agile/iterative methods
]]>
Wed, 01 Aug 2018 00:00:00 PDT 0
<![CDATA[Technical Support Specialist]]> Bayside Solutions is seeking a Technical Support Specialist  to be a part of our partner’ s team in the South Bay Area.

Our partner’ s culture is professional and hard working. They foster longevity and stability within their organization.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Technical Support Specialist

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Key member of the product marketing team providing technical support and effective communication of the use for the product lines.
  • Receive and process inquiries from customers; analyze and resolve customer problems.
  • Identify and distribute product information according to customer needs
  • Manage technical information resources, including database of scientific references, bibliographies, and tables.
  • Act as a technical resource to our international distributors.
  • Data entry: accurately collect and enter customer contact information and scientific data to corresponding databases (SalesLogix CRM and EndNote reference database).
  • Study scientific literature to identify key experimental methods and emerging trends of use.
  • Assist in the generation of technical and promotional product literature (i.e., newsletters, fact sheets, etc.).
  • Participate and contribute to the implementation of product training workshops.
  • Represent client at tradeshows, conferences and events.
  • Perform ad hoc marketing projects.
  • Ability to use of both hands for extended periods of time while performing regular tasks for in-taking orders, including typing and writing.
  • Ability to lift, move and handle materials weighing up to 25 lbs unassisted. Ability to reach overhead.
  • Ability to speak and hear clearly, particularly on the phone or headset.
  • Willingness to travel as needed (10%).

Required Qualifications:
  • BA/BS Degree in Science Related Field Job Experience.
  • 6 months to 2 years of experience in scientific laboratory environment.
  • 6 months to 2 years of Life Science technical support or customer service experience.
  • Excellent communication skills with the ability to speak and write with clarity and structure.
  • Goal oriented with excellent follow through on actions and tasks.
  • Highly driven, independent worker with a strong motivation to succeed. Demonstrated customer service and organizational skills.
  • Demonstrated knowledge and working understanding of life science research, including scientific method • Ability to perform insightful and resourceful problem solving.
  • Proficient with Microsoft Word, Excel, and PowerPoint. Knowledge of reference databases (i.e., EndNote) a plus.
  • Have an understanding of confidentiality.
  • Fluency in languages other than English a plus.
  • Flexible in handling change, meeting a standard of excellence, persistent in pursuing goals despite obstacles and setbacks. Self-awareness of how behaviors can affect our team.
]]>
Tue, 31 Jul 2018 00:00:00 PDT 0
<![CDATA[Manager, Regulatory Affair CMC IV]]> Bayside Solutions is seeking a Manager, Regulatory Affairs CMC IV to be part of our client’ s team in San Rafael. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Manager, Regulatory Affairs CMC IV:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Coordinating the planning, preparation and submission of global regulatory CMC-related submissions for clinical and commercial products such as: post approval variations, Marketing Application(s), Annual Reports, Clinical Trial Applications, and amendments.
  • Developing and/or reviewing regulatory documents to ensure that all submissions are complete, accurate and meet relevant requirements.
  • Creating timelines and tracking deliverables to timelines to ensure that all submissions are submitted on-time.
  • Performing regulatory research and drafting reports summarizing regulatory requirements.
  • Proactively identifying issues and suggesting appropriate strategies to mitigate risks.
  • Ensuring consistent and appropriate communication within the department and with other functional areas.
  • Interfacing with global Regulatory partners, internal cross functional teams, and consultants.
  • Assisting in the preparation for meetings with global regulatory authorities.
  • Attending relevant functional area and project team meetings.
  • Develop excellent relationships with internal functional groups, contract manufacturing organizations, and corporate partners.

Summary of Qualifications
  • BA/BS degree in life sciences, chemistry, molecular biology, or similar is desirable. Advanced degree is a plus.
  • At least  5 years of experience in Regulatory Affairs or a related function such as Quality, Process Development in a global pharmaceutical and/or Biotechnology Company (preferably with exposure to biologic products).
  • Thorough understanding of relevant drug development regulations and guidelines (ie, FDA regulations and ICH guidelines) as well as an understanding of CGMP.
  • Outstanding interpersonal and communication (written and verbal) skills is required.
  • Strong writing and editing skills for technical documentation.
  • Experience with devices or combination products a plus (ie, HFA evaluations, FMEAs).
  • Effective task planning and coordination abilities.
  • Proficient with computer and standard software programs.
]]>
Tue, 31 Jul 2018 00:00:00 PDT 0
<![CDATA[Drug Safety Associate]]> Bayside Solutions is seeking a Drug Safety Associate to be a part of our Client’ s team in South San Francisco. This is a unique opportunity to join a growing team of professionals focused on the treatment of diseases that affect the functionality of an individual.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

 

Drug Safety Associate

Job Benefits:
  • Opportunities to grow and develop within Drug Safety; training from a team of experienced professionals.
  • Competitive compensation and work-life balance.
  • This position is eligible for medical, vision, and dental benefits, paid sick time and 401k.

Summary of Responsibilities:
  • Triages and maintains the Drug Safety box
  • Updates and distributes list of pending cases to Safety team
  • Updates and maintains the SAE tracker
  • Updates and maintains the Case description tracker for medical monitors
  • Maintains the Drug Safety folder in the shared drive
  • Assists in preparing the monthly SAE listing for distribution to the DMC
  • Serves as first level of Quality Control for draft case narratives and queries prior to sending to Drug Safety Manager (DSM) for second QC
  • Sends notification receipt emails to Parexel
  • Assists the DSM in maintaining Issues log with vendors, etc.
  • Assists in preparing ad hoc reports
  • Sends the BLINDED MedWatch  report to CK Regulatory (all reports) and DMC (Initials only) after DSM’ s review and approval

Requirements:
  • Degree in life sciences. Health care professional (pharmacy, nursing or equivalent) is strongly preferred
  • 3 to 5 years of experience in drug safety is strongly preferred
  • Knowledge of adverse event regulatory reporting requirements
  • Experience with drug safety databases, case processing and MedDRA coding concepts
  • Attention to quality focusing on details with enthusiasm toward ways to improve processes
  • Demonstrated ability to work effectively, collaboratively under minimal supervision with a sense of urgency in a dynamic, cross-function matrix environment
  • Ability to solve complex problems and set priorities to complete work
  • Proficiency in the use of relevant computer systems including MS Word, Excel, PowerPoint, and Outlook
  • Safety data base knowledge preferred
  • Strong interpersonal, written and oral communication skills and professionalism

 
]]>
Tue, 31 Jul 2018 00:00:00 PDT 0
<![CDATA[Senior Research Associate]]> Bayside Solutions is seeking a Senior Research Associate to be part of our Client’ s team in San Francisco. This is an opportunity to work with a local Biopharmaceutical start up company, who focus on developing oncology therapeutics across a broad range of tumor types. 

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

 

Senior Research Associate

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize consumable devices that enable leading-edge medical research.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Design and execute experimental efforts in close collaboration with our academic and corporate partners
  • Investigate key target biology mechanisms and test the effects of our novel drugs at both the cellular and molecular level  
  • Develop research projects, cell based assays and implementing new technology
  • Experience in lab operations and be responsible for daily lab operation

Job Qualifications:
  • Bachelor’ s degree with 6+ years of scientific experience in the biopharmaceutical industry or a Master’ s degree with 3+ years of experience
  • Degree in Cellular Biology, Pharmacology or a related field is required
  • Experience in oncology research and in vitro models is essential
  • Experience conducting and developing quantitative human cell-based assays is required
  • Experience conducting and developing quantitative human cell-based assays is required
    • flow cytometry and fluorescence microscopy
    • luminescence and fluorescence-based cell assays
    • CRISPR, si/shRNA based knockdown methods
  • Experience with immune-assays is required
    • western blotting, ELISA and agarose gels
    •   Immunoprecipitation assays
  • Experience with mammalian tissue culture, both adherent and suspension
  • Hands-on proficiency with laboratory automation and microplate-based assay formats is highly desirable
     

 

 
]]>
Fri, 27 Jul 2018 00:00:00 PDT 0
<![CDATA[Research Associate]]> Bayside Solutions is seeking a Research Associate to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world’ s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life-threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • We seek an outstanding candidate to join our Automation Group in Small Molecule Analytical Development, in Small Molecule Pharmaceutical Sciences.
  • Responsibilities include designing and developing a high-throughput screening (HTS) system for excipient chemical compatibility and formulation optimization to support early-phase drug development.
  • Other duties include chemical reactions, salt/crystallinity/polymorph screening, solid state characterization, solubility determinations, and other analytical research studies.
  • The successful candidate will accomplish our mission through innovation, collaboration with our subject matter experts, creative problem-solving, Design of Experiments, and use of state-of-the-art technology including robotic laboratory systems, XRPD, microscopy, UHPLC, mass spectrometry, chiral separations, supercritical fluid chromatography (SFC) and other analytical instruments.

Summary of Qualifications:
  • BS/MS in a relevant scientific discipline (chemistry or chemical engineering, pharmaceutics preferred) with 2 – 6 years’ experience in small molecule chemistry within the pharmaceutical industry.
  • Candidates must have good knowledge of analytical and organic chemistry.
  • A background in lab automation, chromatography (HPLC and data handling/reporting), knowledge of pharmaceutics, solid state characterization or drug discovery are desirable.
  • Candidates should have good problem solving / communication skills, and ability to work in a collaborative team environment.
  • The position requires good organizational and communication skills and the ability to work well as part of a team.
]]>
Fri, 27 Jul 2018 00:00:00 PDT 0
<![CDATA[Associate Scientist, Gene Therapy]]> Our client in Menlo Park is looking to have an Associate Scientist, Gene Therapy join their growing team!

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

 

Associate Scientist, Gene Therapy

Job Benefits:
  • An opportunity to significantly impart the future of the company’ s operations
  • A competitive base salary
  • On the job training, both in person/online

 

Summary of Responsibilities:
  • Develop AAV capsids and/or regulatory cassettes to improve and/or limit transgene expression to certain tissues
  • Independently design and execute experiments following appropriate laboratory procedures and produce competent and reproducible results to a high technical standard
  • Appropriately analyze and interpret results, and communicate scientific data
  • Maintain accurate records with minimum supervision
  • Participate in the development of assays for the characterization of AAV vector products, particularly in terms of expression upon gene transfer, in vitro (in vivo a plus)

 

  Required Qualifications:
  • Ph.D. in the Biomedical Sciences, biochemistry, virology or other relevant discipline. For Scientist position, 2+ years of relevant research experience after advanced degree.
  • Background in the area of gene therapy (in particular of AAV vectors) is a plus
  • Broad knowledge base in molecular biology, biochemistry and immunology
  • Scientific competency as demonstrated by strong publication record in peer-reviewed journals
  • Expertise in a variety of laboratory techniques such as recombinant DNA technology, including qPCR, vectorology, DNA/RNA isolation and analysis; sterile tissue culture techniques; biochemical techniques including, Western Blot, flow cytometry, immunofluorescence, and ELISA
  • Experience with in vivo animal models is preferred and know-how with the baculovirus expression system is a plus
  • Detail oriented with excellent time management skills
  • Must be proactive, co-operative, and willing to work in a small team environment
  • Excellent verbal and written communication skills
]]>
Fri, 27 Jul 2018 00:00:00 PDT 0
<![CDATA[Front Office Assistant]]> Bayside Solutions is seeking a Front Office Assistant to be part of our client’ s team. This is an opportunity to work with a private research university in the South Bay, California.  This Client is known for its academic strength, wealth, proximity to Silicon Valley, and ranking as one of the world' s top-ten universities

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Front Office Assistant

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life-threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Greet Students, staff and other guests when they come into the office. 
  • Answer office phones and respond to questions, referring to the FDS when necessary.
  • Send out mass email notifications
  • Learn and relay complex Housing policies and procedures.
  • Assist students with lockouts by signing out a board key and/or temporary building access card.
  • Sign out hand trucks and vacuums, tracking all activity in the respective log
  • Provide office coverage during the lunch hours and for meetings.
  • Notify students via email of any misdirected mail brought into the office.
  • Prepare keys and other check in materials per instruction of the FDS.
  • Check students in and out, tracking activity via registration cards.
  • Assist the FDS with regular key inventories.
  • Submit in work orders, rekey requests, and other maintenance requests into the system.
  • Assist the FDS with quarter-opening and quarter-closing duties, as necessary.

 

Summary of Qualifications:
  • High school diploma or AA with working experience is acceptable.
  • Successful applicants will be focused, possess a solid attention to detail, and have a personable and welcoming presence.
  • Strong email, phone, and in-person customer service experience essential.
  • Hotel Front Desk/Concierge experience would be a plus.
  • Clear, concise, effective communication with individuals and groups of diverse backgrounds essential.
  • Must be computer-literate and able to learn new systems quickly.
  • Ability to work in fast paced environment with interruptions throughout the day.

 
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Fri, 27 Jul 2018 00:00:00 PDT 0
<![CDATA[Manufacturing Associate I]]> Bayside Solutions is seeking a Manufacturing Associate I to be part of our client’ s team in the Fremont area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Manufacturing Associate I:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Prepare a variety of media and stock solutions that are transferred from tank to bag or tank to tank in order to support cell culture main operations to facilitate proper cellular growth per SOP.
  • Able to follow SOP’ s to perform routine cleaning activities of parts and equipment using manual cleaning methods, designated parts washers, Clean-In-Place (CIP) and COP(Clean-Out-Of-Place) systems.
  • Collect rinse water samples and performing swabs on required equipment for testing.
  • Execute proper documentation and measures to initiate changing over of parts and equipment to be released for use.
  • Performs a majority of operations in a cGMP clean room environment.
  • Practices ergonomic safety and use appropriate personal protective equipment (PPE) in all operations.
  • Documents execution of operations through the Bio Manufacturing Execution System (BioMES), batch record and equipment use logbook using Good Documentation Practices (GDP).
  • Interchanging between electronic and paper documentation procedures.
  • Performs internal support duties including stocking consumables/materials, updating controlled SOP binders, appropriately discarding expired reagents, recognizing and reporting process and equipment anomalies.
  • Reports any issues related to manufacturing performance, process and safety to the team lead or Manager in order to ensure safety and compliance with regulations and cGMPs and to facilitate continuous process improvement.
  • Participates in training and development opportunities in order to gain an understanding of SOPs.
  • Performs routine housekeeping of the manufacturing plant using the 5S organization methodology by using appropriate equipment safety signage, labeling of parts-in-process, sweeping water pools to the floor drain, and picking up parts from the floor.
  • Collaborates within team and department in order to follow best practices and meet department goals.

Summary of Qualifications:
  • Requires a High School Diploma or equivalent plus four (4) years closely related technical experience, preferably in a pharmaceutical or chemicals manufacturing environment.
  • Associates Degree with a minimum of two (2) years closely related technical experience, preferably in a pharmaceutical or chemicals manufacturing environment; or a Bachelors’ degree, preferably in a science or engineering field is preferred with 1+ years of GMP experience.
  • Experience working with established GMP procedures and bulk manufacturing.
  • Technical knowledge of manufacturing systems, methods and procedures.
  • Understanding of cell culture processes. Possess effective troubleshooting skills with equipment and/or process. 
  • Demonstrated ability to be organized and work well in  small work groups. 
  • Must be able to assist in trouble shooting activities and repairs to production equipment under the guidance of more experienced  technicians. 
  • Demonstrated mathematical skills, including the ability to perform addition, subtraction, multiplication, division, and conversions.
  • Detail oriented. Demonstrated ability to read,  comprehend, and follow written instructions. 
  • Demonstrated written and verbal communication skills are required.
  • Must be able to work in a team environment. 
  • Experiences in related biotechnology/pharmaceutical industry strongly preferred
  • Must be able to learn and perform basic computer operations  such as MS Office and Outlook and other computer based software.
  • Preferred skills include experience in: Current Good  Manufacturing Practices, Mammalian cell culture, Bio Manufacturing Execution System (BioMES), Process Control System DeltaV, Laboratory Management Information System (LIMS). 
  • Requires physical activity such as almost constant  standing, walking, eyestrain, etc. Must be able to occasionally lift up to  25 lbs.
  • Works regularly under desirable conditions with some moderately disagreeable conditions in the manufacturing setting.
  • Position requires constant use of computer terminals and routine /  repetitive work.
  • Requires concentration as errors might  cause minor to moderate delays, confusion, or expense to correct; the position has some contact with other departments and the associate must be  able to discuss issues and ideas with an open mind and even temper.
]]>
Fri, 27 Jul 2018 00:00:00 PDT 0
<![CDATA[Research Associate II]]> Bayside Solutions is seeking a Research Associate II to be part of our client’ s team in the South San Francisco area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate II:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Work in the biophysics group supporting projects using Surface Plasmon Resonance (SPR).
  • Provide fragment screens, hit validation, SAR, and mechanism of action studies to support early stage research and discovery programs. 
  • Independently develop, validate, perform, analyze and interpret SPR experiments. 

Summary of Qualifications:
  • BS or MS in Biochemistry, Biophysics, or a related field, preferably.
  • At least 3 years of relevant experience using biophysical or biochemical methods for small molecule drug discovery projects.
  • Quantitative experience in at least 1 biophysical technique (SPR, NMR, crystallography, etc.) and have a solid background in protein biochemistry and biophysics.
  • While the work will be heavily SPR-driven previous experience with that technology is not required as long as the candidate has a significant background in rigorous precision measurement.
  • Individuals with strong organization and communication skills and the ability to work well as part of a team are strongly sought.
]]>
Fri, 27 Jul 2018 00:00:00 PDT 0
<![CDATA[Research Associate I]]> Bayside Solutions is seeking a Research Assistant to be part of our client’ s team in Novato. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Assistant:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Primary responsibility is support for the Assay Services subgroup within Analytical Chem.
  • Documentation of samples received for analysis and performance of a variety of analytical assays with adherence to strict timelines.
  • Assays may include enzyme activity, total protein, cell-based bioassays, chromatography and electrophoresis, done under the supervision of more senior personnel.
  • Assists in the qualification of assay methods and in their transfer to the Quality Control laboratories.
  • Provides major contributions to the evaluation of drug substance and drug product. 
  • Responsible for operational aspects of the laboratory through ordering, equipment maintenance and organization.
  • Receives, documents sample submission and records results for Assay Services in support of a variety of different groups including QCCS, Cell Culture PD, Purification PD and Formulation.
  • Performs analytical assays for samples within and outside the purview of assay services, including enzyme activity, total protein by Bradford or A280, cellular uptake bioassays, gel and capillary electrophoresis and HPLC methods.
  • Under appropriate supervision, assists Research Associates and Scientists in the qualification of assay methods for transfer to the Quality Control Analytical and In-Process laboratories.
  • With increasing experience, develops the capacity to troubleshoot assay methods and to suggest remedies for problems or improvements to the methods.

 

Summary of Qualifications:
  • Four-year degree in a biological or physical science, with typical academic laboratory classes.
  • 0-3 years’ experience in biological or chemical laboratory work.
  • Knowledge and experience in lab processes and procedures.
  • Experience with cell culture sterile technique is preferred.
]]>
Thu, 26 Jul 2018 00:00:00 PDT 0
<![CDATA[Clinical Data Manager]]> Our client in South San Francisco is looking to have a Clinical Data Manager join their growing team! This is an opportunity to work with a great Biotechnology company focused on the discovery and development of therapies for patients with neurodegenerative diseases, including Alzheimer’ s disease, Parkinson’ s disease, ALS and others.

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

 

Clinical Data Manager

Job Benefits:
  • An opportunity to significantly impart the future of the company’ s operations
  • A competitive base salary
  • On the job training, both in person/online

Summary of Responsibilities:
  • Serve as a data management expert and be the CDM lead for assigned clinical studies on multidisciplinary project teams.
  • Deliver high quality data for analysis and study milestones.
  • Reviews protocols from a CDM perspective and provide functional-expert feedback.
  • Oversee data cleaning activities executed by the CRO and ensures protocol-specified guidelines are applied to the review and cleaning of clinical data.
  • Review and approval of database (DB) technical specifications, including eCRF design, user requirements, edit rules/checks, query logic and data validations.
  • Review and approve key clinical data management deliverables, including: Case Report Form (CRF) design, CRF completion guidelines, database design specifications, data entry guidelines, data management plans, edit check specifications, serious adverse event reconciliation plans, medical coding and electronic data transfer agreements.
  • Manage/oversee all vendor activities and staff assigned to Denali studies including consultants to ensure maximal contribution(s) to clinical programs.
  • Manage/oversee study setup, testing and system validation for new studies in partnership with the DM vendor.
  • Oversight of UAT of eCRF build and validation documents, included but not limited to: edit check document, issue logs, UAT summary report.
  • Collaborate with internal Statistical Programming, internal Biostatistics, and internal Medical Monitor on identifying critical variables in the clinical dataset, for protocol-specified endpoints. Coordinate implementing these variables into CRO DM activities.
  • Develop and manage timelines for key clinical data management deliverables in coordination with the clinical data management CRO and Denali project team.
  • Assist in/oversee defining data listings, summary table validation, data specifications and/or process data transfers in preparation for statistical review and/or data management audit.
  • Manage program-wide DM activities (e.g. database design, critical variables, data review listings, data qc activities etc.) to ensure consistent data quality within a program.
  • Monitor vendor performance to ensure timelines and data quality standards are met.
  • Ensure the use of a standard CRF library aligned to CDISC standards when available; or ensure a logical, consistent data format is implemented which enables SDTM mapping.
  • Ensure compliance of clinical data management processes with applicable regulations and guidelines.

Required Qualifications:
  • Bachelor’ s degree or equivalent with a minimum of 5+ years of experience in clinical data management across phase 1- 3 clinical trials.
  • At least 3 years of the overall experience require acting as a study lead data manager.
  • Experience on dose escalation studies is greatly preferred.
  • Neurodegenerative trial experience is greatly preferred.
  • Comprehensive experience working with clinical database systems.
  • Working knowledge of CDISC including CDASH, TAUG and SDTM as well as data privacy regulations e.g. GDPR.
  • Able to work in a fast paced and dynamic environment while effectively managing multiple projects which may have changing priorities.
  • Able to work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors.

 
]]>
Thu, 26 Jul 2018 00:00:00 PDT 0
<![CDATA[Research Associate, Assay Development]]> Our client in Menlo Park is looking to have a Research Associate, Assay Development join their growing team!

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

 

Research Associate, Assay Development

Job Benefits:
  • An opportunity to significantly impart the future of the company’ s operations
  • A competitive base salary
  • On the job training, both in person/online

Summary of Responsibilities:
  • Develop, optimize and help qualify ELISA, enzyme activity, and immunogenicity assays, possibly including cell-based assays
  • Work collaboratively with different research and development departments to evaluate and implement new assay formats and/or technologies
  • Perform testing as needed in support of product characterization.
  • Conduct routine lab maintenance, writing test procedures, SOPs, protocols, technical reports, and summarizing/presenting data at internal and external meetings
  • Maintaining good documentation is required

Required Qualifications:
  • Minimum of a Bachelor’ s degree (preferably a Master’ s) in Biomedical Science, preferably with 2-3 years’ experience working in a biotech company
  • Broad knowledge base in molecular biology or protein work, biochemistry, and gene therapy
  • Background in the area of retinal or genetic diseases is desired and understanding of AAV biology is a plus
  • Experience in qualification/validation of quantitative assays is desired
  • Experience in assay development is desired
  • Expertise in a variety of laboratory techniques such as ELISA, cut-point immunogenicity assays, recombinant DNA technology (cloning, transformation, qPCR, DNA/RNA isolation and analysis) sterile tissue culture techniques (transfection, transduction, maintaining cell lines); biochemical techniques such as Western Blot, flow cytometry, and immunofluorescence
  • Experience in tissue handling is preferred
  • Proficient with MS Office and other commonly used software
  • Knowledge of SoftMaxPro and GraphPad Prism a plus.
  • Ability to understand, implement, and monitor regulatory and safety guidelines applicable to the pharmaceutical industry

 
]]>
Thu, 26 Jul 2018 00:00:00 PDT 0
<![CDATA[Zendesk/UI Developer]]> Zendesk Developer

Industry: Tech

Duration: 3-6+ Month contract (40 hours onsite required – Flexible on schedule)

Location: Walnut Creek, CA

 

Join Us

Bayside Solutions is an industry-leading provider of staff augmentation and consulting services. Since 2001, we’ ve built our company around a single concept – relationships. We focus on the people we serve. We’ re straightforward, consistent and 100% accountable. We deliver intelligent solutions that help our clients and candidates thrive.

 

The Role

We is looking for a Strong Zendesk (Full Stack) Developer to be part of the production operation Team. This team works very closely with all aspects of client production operation.  We is looking for a talented  Zendesk  Developer to be part of the production operation Team. This team works very closely with all aspects of client production operation. 50% of your responsibilities will be working on various projects integrating Zendesk APIs with new screens that show ticketing information and the 50% of your day will be maintaining and creating new users and access to write queues.

Deliverables
  • Collaborate with a small team to develop integrations for the Zendesk user interface.
  • Provide feedback/guidance to the Product team to help build out business requirements.
  • Work with the Engineering team to implement rest APIs to ensure that integrations work correctly.
  • Develop outside-the-box solutions for new internal requests.

You Have
  • Experience with Zendesk Administration
  • Experience setting up users, macros, reports, custom fields/forms, triggers, automations, and dynamic content
  • Zendesk queue management and workflows
  • Experience with Liquid markup language
  • Integrating third-party APIs using Zendesk' s app framework

Competitive Advantage
  • Experience designing web-based applications using Javascript, JQuery, Bootstrap, Node.js and other libraries.
  • Experience working with multiple teams to develop solutions to complex technical issues
  • Agile/SCRUM experience.
  • Experience with Zendesk APIs and App framework.
  • Knowledge of business tools such as JIRA, GitHub, and Slack.
]]>
Thu, 26 Jul 2018 00:00:00 PDT 0
<![CDATA[Case Manager - Customer Service Representative]]> Bayside Solutions is seeking a Case Manager-Customer Service Representative to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world’ s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Case Manager

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life-threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Provides customer focused reimbursement support to patients, pharmacists, physicians and internal sales force.
  • Educates, informs, and assists patients and providers to navigate through the reimbursement process for the assigned product.
  • Identifies barriers to reimbursement and continually identifies and recommends program efficiencies to the Supervisor to promote high quality of work by Access Solutions/GATCF staff.
  • Identifies and facilitates referrals to alternative coverage options and financial assistance programs for patients who are underinsured or require copy assistance.
  • Establishes relationships with appropriate stakeholders including internal & external partners.
  • May conduct necessary benefits, coverage and payer research/investigations to ensure appropriate resources, compliance with payer appeal policies, practices, timelines.
  • Educates, informs and generally assists patients and their families, as well as other related external or internal parties on how to navigate the appeals process.
  • This position may require some travel and flexibility in work shift
  • Periodic mandatory overtime throughout the year is required. This may include, but is not limited to, high referral season, new product or system launches, enrollment renewals, new line extensions, or any unexpected surge in volume or backlog situations.
  • Workdays are M-F, but may include weekends as needed.

Summary of Qualifications:
  • High school diploma or AA with five years of working experience is acceptable.
  • Bachelor’ s degree is highly preferred with one to two years of experience.
  • A minimum of 1-2 years of data entry is preferred.
  • Proficient in all aspects of reimbursement (i.e., benefit investigations, payer reimbursement policies, regulatory and administrative rules).
  • Demonstrates effective problem-solving skills and provides excellent customer service.
  • Excellent investigational and analytical skills with a proven ability to communicate effectively in both written and verbal format.
  • Ability to work collaboratively in a team structure and responsibly delegates next steps to appropriate team members.
  • Must be able to work in a fast paced environment, multitask, and maintain attention to detail.
  • Must have a reliable mode of transportation.
  • Must be able to work effectively under pressure and prioritize tasks.
  • Must be able to follow written Standard Operating Procedure.
  • Recommended experience with Mac operating systems.
]]>
Wed, 25 Jul 2018 00:00:00 PDT 0
<![CDATA[Sr. Linux Software Engineer (RAID)]]> Client Industry: Data Storage

Location: Irvine, CA

Position: Software Engineer (Linux)

Terms: 6 months contract to hire

About Us: Founded in 2001, Bayside Solutions was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

 

About the role: As a Software Engineer, you will be involved developing and delivering new features high performance network storage products and services for client solutions. In this role, you are required to able to read code proficiently more than writing the code. You will play a key role in the design, development, testing and deployment of high performance, high quality, secure and fault-tolerant software running on network storage devices and collaborate extensively in a cross functional capacity.

 

Must Have Skills:
  • At least 7 years of relevant experience and a Bachelor’ s degree or its equivalent OR 4+ years of relevant experience and a Master’ s degree.
  • Relevant experience in the development of high performance Linux-based storage systems.
  • Must be able to read code /scripts and make modifications to open source code (mainly in bash, perl, python, Golang & Javascript (for UI/UX) or C/C++).
  • Strong understanding of how these Open Source packages operate within Linux, Linux kernel internals, RAID, TCP/IP etc are crucial for these positions.
  • Experience in RAID - software RAID (MD/BTRFS/ZFS) & file-systems like EXT4, BTRFS, NTFS, HFS.
  • Experience with arm & x86 hardware architectures.
  • Strong Linux diagnostic and troubleshooting skills.
  • Experience in Support & Field analysis (FA).
  • Proven ability to make solid, independent technical decisions for high performance, low resource server software.
  • Experience with Open Source Software Integration.
  • Strong knowledge in Linux Kernel and Linux-based OS like Debian.
  • Programming languages: C++, PHP, Javascript, Golang, Python, Bash.
  • AWS Cloud experience is a plus.
  • Agile software development using SCRUM or Kanban is a plus.
]]>
Wed, 25 Jul 2018 00:00:00 PDT 0
<![CDATA[Senior Front End Developer]]> Senior Front End Developer

Location: Sunnyvale

Contract-to-hire

Join Us

Bayside Solutions is an industry-leading provider of staff augmentation and consulting services. Since 2001, we’ ve built our company around a single concept – relationships. We focus on the people we serve. We’ re straightforward, consistent and 100% accountable. We deliver intelligent solutions that help our clients and candidates thrive.

The Role

This person brings a solid understanding and genuine passion for software development, best practices and keen focus on the customer. In addition to a strong technical background, the ideal candidate must possess confident interpersonal skills and an eye toward collaboration. The position requires effective communication, both written and verbal, including the ability to work well with stakeholders from a wide range of backgrounds with varying levels of technical knowledge. It’ s important for this person to be able to establish trusting relationships within a diverse team and across organizations. This role must focus on delivering while having the agility to adjust and thrive in a dynamic environment.
 
  • Bachelor’ s Degree in Computer Science or relevant experience
  • Minimum of 3-4 years of professional software development experience with backend and frontend development teams working on complex development projects
  • Strong knowledge and experience designing and developing scalable frontends using React and Node.js
  • Demonstrated background developing innovative solutions for dynamic web sites - how they scale, how they work with other services, and how they may break
  • Dedicated problem-solver who can work in a fast paced environment where multiple releases are a fact of life
  • Ability to size technical efforts accurately
  • A focus on quality, with experience writing unit tests and collaborating with quality engineering to develop test plans
  • Experience collaborating with other team members in multiple teams diagnosing and debugging complex systems, and participating in investigating build, deployment and operational issues
  • Knowledge of Linux stack, and comfort with Bash commands
  • Experience with web application security and incorporating security into the software development lifecycle
  • Solid working knowledge of source version control software (Subversion, Git)
  • Experience collaborating with other technical teams on DevOps responsibilities for application deployment, performance, monitoring, reliability and scalability
  • Willingness to take the initiative to solve problems
  • Proven capabilities to work under pressure and tight deadlines to solve critical issues
  • Able to work equally well with people in creative and technical positions
]]>
Tue, 24 Jul 2018 00:00:00 PDT 0
<![CDATA[HPC/Cloud Computing Sr. Systems Admin]]> Client Industry: Data Storage

Location: Irvine, CA

Position: Senior System Administrator – Cloud Computing

Terms: 6 months contract to hire

About Us: Founded in 2001, Bayside Solutions was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

About the role: Our client in Irvine is looking for a Senior Systems Administrator to aid with the deployment and support of High Performance Computing Solutions along with applications support. You will work cross functionally with a diverse team of development engineers across the globe. This position requires expertise within Linux/Unix computing solutions. The HPC solutions are deployed on premise and in cloud and comprise of both CPU and GPU based solutions. As a Senior System Administrator, you will be an SME for the UNIX/Linux operations and for the engineering application support teams. In this role, you will be tasked with providing expertise on best in class scalable deployment solutions and be an advocate for Open Source HPC and Linux solutions.

QUALIFICATIONS: 
  • 10+ years of experience in enterprise level Linux/UNIX systems administration, provisioning, configuration, troubleshooting, and monitoring with tools such as Nagios, Zenoss, SNMP, Ansible.
  • Experience with installation, management and use of software such as compilers, scientific applications, batch schedulers, job resource, and application license and utilization managers.
  • Experience with the installation, configuration, management, and use of high performance computers such as clusters of Linux boxes, large SMPs and large scale solutions of 1000’ s of computing cores.
  • 3+ years of recent experience with Amazon Web Services and/or Microsoft Azure cloud environments.
  • Must possess strong documentation skills.
  • Must be able to work in a rapidly changing environment.
  • Proven ability to influence and/or lead high performing/ geographically dispersed teams.
  • Excellent analytical, problem solving, and troubleshooting skills to manage complex process and technology issues.

EDUCATION:
  • BS/BA preferred or equivalent experience.
]]>
Tue, 24 Jul 2018 00:00:00 PDT 0
<![CDATA[QC Analyst]]> Bayside Solutions is seeking a QC Analyst to be part of our client’ s team in Marin County. This is an opportunity to work with one of the largest Biopharmaceutical companies in the world developing innovative medicine to improve the quality of patients’ lives.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

QC Analyst:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • The Contract Analyst under direct or minimal supervision, is responsible for performing biochemical, physical, and chemical evaluations of process development, lot release, and stability samples.
  • Contract Analysts work independently on assays that he/she has mastered.
  • They must be able to work on projects with little supervision, write and execute method validation and special studies, and have some oversight of a product line.
  • Perform, under moderate supervision, biochemical/physical/chemical analyses of test samples under cGMP to meet specified timelines.
  • Work independently on assays that he/she has mastered.
  • Evaluate data against defined criteria/specifications.
  • Maintain laboratory supply inventories.
  • Maintain the laboratory in an inspection-ready state.
  • Provide support for glassware cleaning and other routine laboratory functions/chores for the QC laboratory.
  • Develop and maintain proficiency in a broad range of test methods.
  • Assist in the revision of written procedures as assigned.
  • Assist in the preparation of routine and non-routine study protocols and reports. 
  • Train other analysts in areas of expertise.
  • Develop familiarity concerning cGMP, 21CFR, USP, EP, and ICH regulatory

Required Qualifications:
  • Bachelor' s Degree in science (major in biology-biochemistry-chemistry) 0-2 years of experience
  • At least one year in a cGMP/GLP laboratory; quality control experience is preferred.
  • Ability to follow written instructions and to perform tasks with direct or minimal supervision.
  • Familiarity with use of a computer: e.g., Proficient in Windows, Microsoft Word, Excel.
  • Good written, verbal, and communication skills.
  • Strong documentation skills
]]>
Mon, 23 Jul 2018 00:00:00 PDT 0
<![CDATA[Data Scientist]]> Bayside Solutions is seeking a Data Scientist to be part of our client’ s team in the Fremont area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Data Scientist

Job Benefits:
  • An opportunity to join a genomics sequencing organization. 
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Focus on data capture, management and analysis using innovative software/services.
  • Work cross-functionally to translate scientific workflows into process design with the help from the vendors and internal partners.
  • In charge of creating process design/platform template, data capture, import data from different database/excel/other forms, help to set up API to export data from interface to statistical software, interpret the statistical analysis as needed.
  • Learn the routine biopharm processes/practices as well as exposure to cutting-edge technologies generating different formats of data.

  Required Qualifications:
  • B.S./M.S. in statistics, computer science, chemical engineering, biology, analytical chemistry or related field; must have completed 12 credit hours within a related major and/or other related coursework; overall, cumulative GPA (from last completed quarter) must be at least 3.2 (on 4.0 scale) or better. 
  • Proficiency using Excel, python and/or scripting languages for data capture, analysis and reporting.
  • Demonstrated data-driven capability to identify and solve scientific problems.
  • Strong communication and organization skills.
  • Highly self-motivated, be flexible and willing to learn. 
  • Experience in biopharma R&D or knowledge about process development is a plus.
  • Experienced using JMP, R, Spotfire, SIMCA or other software for multivariate data exploration or analysis.
  • Experience in advanced data and/or statistical treatments such as machine learning.
  • Experience in Design of Experiments (DoE), Partition of Variance and associated statistical methodologies highly sought.
]]>
Mon, 23 Jul 2018 00:00:00 PDT 0
<![CDATA[QA Script Tester]]> Position: QA Script Tester (pentesting)

Location: Sunnyvale, CA

Duration: 6 months contract

Join Us
Bayside Solutions is an industry-leading provider of staff augmentation and consulting services. Since 2001, we’ ve built our company around a single concept – relationships. We focus on the people we serve. We’ re straightforward, consistent and 100% accountable. We deliver intelligent solutions that help our clients and candidates thrive.

Role
Looking for dynamic, creative individuals who possess experience as a QA Script tester

Must have Skills:
  • QA Script (heaving shell scripting)
  • UNIX
  • Pentesting

Desired Skills:
  • Forensic analysis a plus
  • Working on DevOps team internally
  • (2-5) years experience

Education:  Bachelor’ s Degree
]]>
Fri, 20 Jul 2018 00:00:00 PDT 0
<![CDATA[Python/DJango Developer]]> Position:  Python Developer (Django)

Location: Sunnyvale, CA

Duration: 6 months contract

Join Us
Bayside Solutions is an industry-leading provider of staff augmentation and consulting services. Since 2001, we’ ve built our company around a single concept – relationships. We focus on the people we serve. We’ re straightforward, consistent and 100% accountable. We deliver intelligent solutions that help our clients and candidates thrive.

Role
Looking for dynamic, creative individuals who possess heavy experience in Python/ Django and Angular/React/Vue JS 

Must have Skills:
  • Python Engineering
  • Django emphasis
  • Must know data structures
  • 2-10 yrs in development using  Python/Django
  • Experience working with DevOps teams

Education:  Bachelor’ s Degree
]]>
Fri, 20 Jul 2018 00:00:00 PDT 0
<![CDATA[Process Scientist II]]> Bayside Solutions is seeking a Process Scientist II to be part of our client’ s team in the Fremont area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Process Scientist II

Job Benefits:
  • An opportunity to join a genomics sequencing organization. 
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Work within a highly motivated team to deliver high quality results within a fast-turnaround, as part of process analytics.
  • Day to day duties of the scientist include the opportunity to apply a variety of analytical techniques to support process development.
  • Relevant techniques are UV/Vis, amino acid analysis by UPLC, affinity assays by Octet and/or HPLC, purity by capillary electrophoresis (CE or LabChip), size exclusion chromatography by UPLC and charge variants by cation exchange chromatography.
  • Other potential techniques are immuno-based assays for binding and impurity analysis (ELISA, Octet, Biacore), as well as qPCR.
  • Independently to execute protein analytical work in a fast pace environment.
  • Perform data analysis and interpretation, and making internal technical presentations. 
  • Work in a highly interdisciplinary and collaborative environment as part of the Process Science team.

  Required Qualifications:
  • BS with 4+ years in protein analytics, MS with2+ years’ experience.
  • Hands-on experience in protein analytics, with experience in 1 or 2 of the above described analytical assays.
  • Good written and oral communication skills.
  • Ability to work in a team environment.
]]>
Fri, 20 Jul 2018 00:00:00 PDT 0
<![CDATA[Senior Manager, Project and Portfolio Management]]> Our client in Menlo Park is looking to have a Senior Manager, Project and Portfolio Management to  join their growing team!

Bayside Solutions is seeking a highly motivated, professional and experienced Senior Manager, Project and Portfolio Management to be a part of a high-growth organization. This is a unique opportunity to join a growing team in a forward thinking biotech company to work with unique bio-engineer microbes for their clientele.

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Senior Manager, Project and Portfolio Management

Job Benefits:
  • An opportunity to significantly impart the future of the company’ s operations
  • A competitive base salary
  • On the job training, both in person/online

Summary of Responsibilities:
  • Be responsible for managing one or more highly complex development projects; co-lead early stage development team(s) with a project team leader to drive preclinical assets into the clinic.
  • Work closely with the project team members representing preclinical, clinical, regulatory, and operations, CMC, quality, legal departments in a matrix team environment to develop concise strategic development proposals, integrated project plans, and manage and track key project deliverables.
  • Provide regular project team deliverables and progress updates to Senior Management.
  • Work with the Project Leader to proactively facilitate team discussions on project strategies, short-term and long-term project planning, opportunities for expediting timelines, identification resource constraints, and proactively identify complex project issues and risks, and assure appropriate escalation.
  • Schedule and facilitate Cross-Functional Project Team meetings using meeting management best practices to drive cross-functional communication, timely and effective decision-making, and successful execution of program objectives. Develop agendas and summarize key meeting discussions and decisions (meeting minutes).
  • Develop, track and maintain project development timelines, deliverables and milestones; including understanding and communicating inter-dependencies and critical path activities.
  • Develop, track and maintain project publication plans, work with team to identify key conferences and journals, coordinate publication development and publication gap analysis.
  • Work closely with and build strong working relationships with cross-functional team members to develop a collaborative team environment and manage timelines for regulatory submissions (IND/NDA/BLA/MAA, etc.).
  • Assists in the review of project team regulatory documents and SOP revisions, if relevant.
  • Work closely with Sr. Director PPM in ongoing enhancements and development of team processes, structures, and project reporting tools.
  • Report into the Senior Director, Project and Portfolio Management.

Requirements of Qualification: 
  • BS required; Master’ s Degree Preferred.
  • 5+ years of project management experience, with a minimum of 3 years in early and/or late stage drug development project management.
  • Exposure to early-stage programs (pre-clinical though Phase I/II proof-of-concept) essential; and exposure to late-stage programs (Phase II/III pivotal) a plus.
  • Able to work independently with minimal oversight
  • Proven ability to balance the strategic needs of the program with tactical day-to-day activities.
  • Ability to analyze complex activities and information to help guide decision-making that meets the overall objectives and long-range plans of projects and the organization
  • Excellent people (soft) skills, diplomacy and positive influencing abilities.
  • Gene therapy and rare disease experience preferred.
  • Ability to proactively predict issues and solve problems, identify risks.
  • Ability to drive decision-making within a multi-disciplinary, multi-regional, matrix team.
  • Understanding of US and EU Regulatory requirements.
  • Outstanding communication, planning and organizational skills.
  • Highly collaborative team player who fosters open communication and able to facilitate urgent needs.
  • Successful track record of creating and managing accurate timelines and the use of project software (Microsoft Project, Visio, PowerPoint and Excel, etc.).

 
]]>
Fri, 20 Jul 2018 00:00:00 PDT 0
<![CDATA[Preclinical Study Monitor]]> Bayside Solutions is seeking a Preclinical Study Monitor for our client in Peninsula!

Our client in Menlo Park, CA  is looking for Preclinical Study Monitor. The successful candidate will perform preclinical development activities (pharmacology and toxicology) for IND-enablement of gene therapy products in addition to facilitating and executing preclinical development plans for future pipeline products. The candidate must possess integrity, proven systematic drug development thinking, exceptional writing and strong organization and communication skills with the ability to work independently in a dynamic and cross-functional company.

Our Company Bio:
Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at  www.baysidesolutions.com.

Preclinical Study Monitor
  • An opportunity to join a patient-focused organization with the goal to provide patients and physicians with improved treatment options.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, commuter benefits, and 401K.

 Summary of Responsibilities:
  • Manage operational aspects and timeline of preclinical studies (GLP and non-GLP) for inclusion in regulatory submissions, including pharmacology, toxicology, and biodistribution/shedding studies.
  • Monitor conduct of preclinical studies with CROs, both through site visits and regular conference calls. Follow-up on action items with CROs to ensure on-time delivery to the Adverum team.
  • Establish study timelines and insure that all study related activities are being addressed.
  • Write and edit preclinical study protocols and reports.
  • Work closely with the members of Preclinical Development on therapeutic development strategies.
  • Work closely with CROs to ensure that all studies are performed in a high quality, timely, and scientific manner.
  • Maintain a current understanding of pharmacology and toxicology literature and methodology, as well as the scientific literature related to the specific drug development projects.
  • The Study Coordinator will report to the Associate Director, Preclinical Development.

Required Qualifications:
  • Bachelor’ s degree in Biological Sciences, Toxicology, Pharmacology, or a related discipline.
  • 5 years drug development experience, with minimum 3 years working in industrial pharmaceutical pharmacology/toxicology/safety assessment.
  • Proven experience in coordination, organization, analysis, and documentation of preclinical studies.
  • Ability to synthesize, organize, and analyze diverse, multidisciplinary data sets using Excel/ GraphPad/ PowerPoint or similar software
  • Excellent scientific writing and editing as well as written/oral communication skills with several years of professional experience in medical or scientific writing.
  • The ability to work independently and to collaborate with a multi-disciplinary group in a goal- and team- oriented setting.
  • Availability to travel to CROs for study monitoring activities.
  • Proficiency with MS Office and common laboratory software (GraphPad Prism, etc.).
  • Working knowledge of FDA/ ICH guidelines relevant to preclinical development is a plus.
]]>
Thu, 19 Jul 2018 00:00:00 PDT 0
<![CDATA[Director of Medical Writing]]> Our client in Menlo Park is looking to have a Director of Medical Writing join their growing team!

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

 

Director of Medical Writing

Job Benefits:
  • An opportunity to significantly impart the future of the company’ s operations
  • A competitive base salary
  • On the job training, both in person/online

Summary of Responsibilities:
  • Lead document review and comment resolution meetings with cross-functional teams according to the timeline
  • Prepare scientific literature searches, scientific abstracts, posters, manuscripts, Advisory Committee presentations, exhibits, etc. as needed
  • Build and maintain knowledge base in both Medical Writing expertise and therapeutic area understanding to ensure the overall document quality
  • Oversee document preparation activities and timeline development
  • Use scientific expertise to write, review, and edit science-based reports such as clinical protocols, Investigator’ s Brochures, clinical study reports, risk/benefit analysis and integrated summaries, IND sections, Briefing Documents, annual reports
  • Meet ICH, GLPs, and GCPs guidelines, develop a writing style guide and template, as needed
  • Direct, train, and assist other medical writers in the writing and editing and technical aspects of clinical and regulatory document development
  • Work with key company stakeholders to help integrate nonclinical and clinical trial data into concise and compelling reports
  • Work with cross-functional teams to be sure that all deliverables are in accordance with regulations, standards, guidelines and timelines

Required Qualifications:
  • BS, MS, RN, PharmD or doctorate in a scientific or medical field (an equivalent combination of education and experience may be considered)
  • A minimum of 10 years’ experience as a Medical Writer in the pharmaceutical, biotech industry or clinical research organization
  • Previous management experience in the medical writing function
  • Demonstrated leadership capability and strong writing skills
  • Demonstrates strong organizational skills and ability to work collaboratively in a cross-functional team environment
  • Experience working on INDs, BLAs, and other regulatory submission activities
  • Exceptional oral and written communication skills
  • Strong understanding of drug development, clinical study design, regulations (FDA and EU), ICH and other guidances, and scientific principles
  • Ability to effectively work in a multi-disciplinary team, build and maintain effective partnerships
  • Able to manage timelines for document development, review and completion according to expectations
  • Detail oriented and dedicated to producing high-quality documents
  • Strong communication, negotiation and interpersonal skills
  • Experience mentoring/training other writers
  • Proficient in Word, Excel, PowerPoint, the use of templates, email, and internet
]]>
Thu, 19 Jul 2018 00:00:00 PDT 0
<![CDATA[Director of Facilities]]> Our client in Menlo Park is looking to have a Director of Facilities join their growing team!

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

 

Director of Facilities

Job Benefits:
  • An opportunity to significantly impart the future of the company’ s operations
  • A competitive base salary
  • On the job training, both in person/online

Summary of Responsibilities:
  • Will be responsible for the effective uninterrupted support of Facilities operational activities
  • Will be responsible for the Plant facilities budget
  • Ensures and conducts proper staff training
  • Develops resource plans that meet operational goals in terms of safety, quality, output and cost
  • Responsible for maintaining the facility in compliance with local, county, state, and federal regulations
  • Manages, plans, and coordinates the preventive maintenance and the repairs of the electrical, mechanical, HVAC, security systems as well as other related building systems
  • Manages staff of maintenance technicians and oversees contractors to ensure their compliance with applicable federal, state and local regulations and laws, company policies and procedures, and current Good Manufacturing Procedures
  • Makes project/work assignments with communication of the expected timeline and monitors the progress against the timelines
  • Plans work schedule to maintain safe, clean, and healthy conditions on company property to achieve the best working environment possible for employees and visitors.
  • Provides troubleshooting support as needed
  • Effectively communicates with clients, regulatory agencies (FDA, EMA etc.) and internal project teams
  • Solves complex regulatory, mechanical, electrical, and electronic issues/questions.
  • Responsible for optimizing resource allocation and prioritization of maintenance activities
  • Provides overall directions and sets priorities for the site improvement projects and activities
  • Plans and coordinates major maintenance activities including scheduled Plant shutdowns
  • Conducts scheduled performance reviews and assessments for direct reports
  • Represents site Facility Operations organization at all internal and external audits
  • Ensures equipment availability is adequate to meet the organization’ s requirements.  Central plant services (Chilled Water, Heating Hot Water, DI Water). HVAC air distribution and management, Building Management System, Standby Generator, support equipment. Chillers, boilers, air handlers, exhaust fans, pumps, sensors, fan coils, emergency generator, air compressors, vacuum pumps, DI water plant, building controls, setting and schedules. Optimize energy.

Required Qualifications:
  • BS degree with 6+ years of pharmaceutical facilities experience and 3+ years of supervisory experience.
  • Strong leadership, performance management and employee development skills.
  • Strong facility-related (e.g. mechanical, electrical) assessment and troubleshooting skills.
  • GMP experience and safety knowledge (understanding of OSHA requirements)
  • Computer literate with a good knowledge of MS Office packages. Preventative Maintenance, BMS software a plus
  • Strong project management skills (i.e. budget tracking, schedule development and adherence, project reporting, etc.)
  • Demonstrated communication, administrative and leadership skills with ability to work well with other departments, and effectively and efficiently lead in a team environment.
  • Proven ability to manage multiple priorities in a fast-paced environment.
  • Ability to understand, implement, and monitor regulatory and safety guidelines applicable to the pharmaceutical industry.

 
]]>
Thu, 19 Jul 2018 00:00:00 PDT 0
<![CDATA[Senior/Principal Scientist, Preclinical Development]]> Our client in Menlo Park is looking to have a Senior/Principal Scientist, Preclinical Development join their growing team!

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Senior/Principal Scientist, Preclinical Development

Job Benefits:
  • An opportunity to significantly impart the future of the company’ s operations
  • A competitive base salary
  • On the job training, both in person/online

Summary of Responsibilities:
  • Edit and write preclinical study reports
  • Collaborate  with members of the Preclinical Development to evaluate therapeutic candidates in normal and ocular diseased models
  • Design preclinical studies (GLP and non-GLP) for inclusion in regulatory submissions, including pharmacology, toxicology, and biodistribution/shedding studies
  • Monitor conduct of preclinical study with CROs
  • Write preclinical sections for preclinical submissions
  • Work closely with other functional areas and colleagues to insure that all studies are performed in a quality, timely and scientific manner
  • Collaborate with other project team members on development strategy
  • Develop, and write, position papers on safety, pharmacology and mode of action to support product development
  • Develop safety-related issue mitigation or resolution plans and coordinate execution of the experimental plan as required
  • Prepare and edit non-clinical documents for regulatory submission (e.g. IBs, and regulatory briefing documents)
  • Maintains a current understanding of pharmacology and toxicology literature and methodology, as well as the scientific literature related to the specific drug discovery projects
  • The Scientist will report directly to the Head of Preclinical Development

Required Qualifications:
  • Ph.D. in Biological Sciences, Toxicology, Pharmacology
  • 6-8 years drug development experience, with minimum 3 years working in industrial pharmaceutical toxicology/safety assessment drug development
  • Proven experience in design, coordination, analysis and documentation of preclinical studies
  • Ability to synthesize and interpret diverse, multidisciplinary data sets
  • Extensive knowledge/understanding of pharmacology pathways and MoAs relating to the IND-enablement of biologic programs with preference given to gene therapy programs
  • Excellent scientific writing and editing as well as written/oral communication skills with several years of professional experience in medical or scientific writing
  • The ability to work independently and to collaborate with a multi-disciplined group in a goal- and team- oriented setting is required
  • Proficiency with MS Office and common laboratory software (GraphPad Prism, etc.)
]]>
Wed, 18 Jul 2018 00:00:00 PDT 0
<![CDATA[Research Associate II]]> Bayside Solutions is seeking a Research Associate II to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate II

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • A position in Antibody Discovery Group of Antibody Engineering Department.
  • The candidate must be scientifically driven and will perform and handling various projects focusing on  high throughput screening assays (ELISA and FACS), tissue culture and  data analysis.
  • Qualified candidate should have proven ability to execute and interpret variety of experiments and solving problems rapidly.
  • The person in this position will also frequently interact and communicate  with other collaborators to present the results in various forums. 

Summary of Qualifications:
  • The candidate must have BS/MS degree in Immunology, Molecular Biology, Biochemistry or related fields
  • Preferably 3+ years’ experience in immunology or cell biology research from  academic or  pharmaceutical industry. 
  • Good knowledge of  cell biology  and immunology as related to antibody discovery.
  • Ability to handle cells, cell based assays, and good at FACS analysis.
  • Good computer skills and analysis software skills such as Diva, CellQuest and FlowJo.
  • Must be good at troubleshooting with strong attention to detail.
  • Must be a highly motivated team player who works well with others and with strong interpersonal skills.
  • Ability to follow detailed verbal and written instructions.
  • Requires strong verbal communication, writing, and listening skills.
  • Must be an organized self-starter with ability to multi-task, and meet timelines efficiently and productively.
  • Flexibility and an eagerness to learn is required.  
]]>
Wed, 18 Jul 2018 00:00:00 PDT 0
<![CDATA[Research Associate, Fermentation Technology Development]]> Our client in the East Bay is looking for a Research Associate - Fermentation  Operations team member  to join their team!
Bayside Solutions is seeking a highly motivated, professional and Research Associate to be a part of a fermentation operations team with a  high-growth organization. This is a unique opportunity to join a growing team in a forward thinking biotech company to work with unique bio-engineer microbes for their clientele.    A successful RA, will be a part of the Fermentation Operations team  and  will help create new technologies, bring in  cutting edge protocols described in  the literature, and improve protocols to provide newer and better workflows to their microbe engineering Factory.   This person will be focusing on the continual improvement of both high throughput screening and fermentation workflows. These associates are required to be able to identify and implement improvements in existing processes and establish protocols for new programs. 
The culture is very start-up minded and looking for candidates that will push their program forward and to be innovative, take initiative.

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate, Fermentation Operations

Job Benefits:
  • An opportunity to significantly impart the future of the company’ s operations
  • A competitive base salary
  • On the job training, both in person/online

Summary of Responsibilities:
  • Experiment design and execution, preparing reagents, collecting and analyzing data to present to a technical audience.
  • Setup, running, tear down and turn-around of lab scale fermenters/bioreactors, including work in off hours.
  • Preparation of complex media and sterilize equipment with multiple variations for both plates and fermenters.
  • Operation of multiple types of robotic systems, including but not limited to, liquid handlers, colony pickers, barcoders, and automated plate readers and improvement of robotic scripts.
  • Development and implementation of new data tools in collaboration with automation and software teams.
  • Work with data capture systems to store data and metadata about the experiments
  • Establishment of new assays to measure in-process fermentation samples and samples from high throughput strain screening.
  • Process samples in plate-based and HPLC assays in collaboration with the analytical chemistry team.

  Required Qualifications:
  • BS in Life Sciences with 1- 6 years' experience working with bioreactors or fermentors.
  • Familiarity with a variety of bench scale bioreactors/fermentation units is desired.
  • Experience with a variety of microbes, a variety of fermentation processes (aerobic, microaerobic, and anaerobic), and a variety of fermentation products (proteins, small molecules).
  • Experience using lab automation (Beckman, Tecan, etc.) to enable complicated or high-throughput protocols.
  • Experience with programming, familiarity with statistical concepts, or experience with analysis software such as JMP.
  • A strong understanding of cellular physiology to troubleshoot and improve existing cultivation models.
  • A proven track record in identifying and implementing process improvements.
  • Experience working with SOPs for bioreactor/fermentation and bioreactor/fermentation-related processes.
  • Experience running, setting up and troubleshooting processes required to build out a bioreactor/fermentation.
  • Use data analysis tools to understand process variations and manage process controls, and to identify microbes with improved performance.
  • Knowledge of basic statistic including JMP, and the use of manufacturing practices such as control charts, Lean, and 5S.
]]>
Wed, 18 Jul 2018 00:00:00 PDT 0
<![CDATA[Material Specialist]]> Bayside Solutions is seeking a Material Specialist to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Material Specialist:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Will work under the supervision of the Materials Operations supervisor.
  • The Materials Specialist is responsible for the accurate receipt, verification, record keeping, distribution, and shipment of materials and goods.
  • Work performed will include acceptance of incoming materials by ensuring paperwork is accurate and materials are received in good conditions.
  • Observe proper handling, storage and/or temperature requirements
  • Pack materials for proper shipping conditions
  • Prepare shipping documents, prepare manifests for hazardous materials, and perform campus pick-ups of outgoing shipments.
  • Prepare receiving documents, route receiving information, prepare outgoing shipments.
  • Perform x-ray scanning of packages, process and receive radioactive materials.
  • Apply proper placards.
  • Apply asset tags to capital equipment.
  • Operate material handling equipment in a safe and appropriate manner
  • Maintain equipment and work areas for cleanliness.
  • Provide for internal distribution of Good Manufacturing Practices materials to company facilities
  • Independently follows Current Good Manufacturing Practice procedures and clearly understands the importance of accurate GMP documentation.
  • Observe all health and safety guidelines.

Summary of Qualifications:
  • Valid California Driver' s License Required.
  • Previous experience with packaging equipment; Xray equipment\Attention to detail\Adherence to safety procedures.
  • Adjust to schedule changes, work overtime as necessary and float between groups as needed to support operations.
  • Proficient in Word, Excel, gDocs for data entry.
  • Adheres to appropriate laws, client regulations and programs, and documentation procedures.
  • Serve as a liaison between customers and warehouse staff.
  • Complete training records in a timely manner.
  • Utilize time wisely to maximize productivity.
  • Meet timeline commitments and inform others of status, issues, and customer requests as necessary.
  • Ensure that all work is completed by end of day.
  • Communicates clearly and effectively, both verbally and written.
  • Ability to be reliable and punctual.
  • Adheres to safety guidelines as required for your area.
  • Individual will be driving Genentech vans and/or bobtail trucks. Forklift certification is a plus. Individual will be driving on the streets.
]]>
Wed, 18 Jul 2018 00:00:00 PDT 0
<![CDATA[Service Desk Technician]]> IT Service Desk Support

Industry: Financial Services

Duration: 6 Months Contract to Hire

Location: Camas, WA

Interview Process: Phone, Onsite

 

Join Us

Bayside Solutions is an industry-leading provider of staff augmentation and consulting services. Since 2001, we’ ve built our company around a single concept – relationships. We focus on the people we serve. We’ re straightforward, consistent and 100% accountable. We deliver intelligent solutions that help our clients and candidates thrive.

 

The Role
We are looking for a talented IT Service Desk Support to join our client’ s infrastructure support team.  This candidate will be providing support via email, phone, and in-person to over 2500 corporate end users.  You will also act as liaison between end users and internal IT teams assisting with resolving other infrastructure issues.

We Have
  • Provide 2nd and 3rd level mobile device support (BES & Apple Configurator): Laptops, Blackberry and iPhones
  • Responsible for desktop imaging (MDT) and physical deployment
  • Support and fix desktop (hardware/software) issues
  • Troubleshoot, diagnose and resolve complex PC and network problems
  • Support Windows 7 environment
  • Be an advocate for the end users on support issues
  • Maintain a high level of courteous customer service at all times.
  • Willingness to learn and grow, technically
  • Ability to work independently and as a team

You Have
  • Associate degree or 3+ years of IT experience providing tier 1/tier 2 support in a fast paced corporate enterprise environment
  • Experience with telecom incidents, desktop (hardware/software), third-party software/hardware applications, and home office configurations.
  • Experience troubleshoot, diagnose and resolve complex PC and network problems.
  • Experience working within Windows 7 and familiarity with Citrix desktop environment
  • The ability to identify patterns and investigate mission critical solutions. 
  • Experience of handling tickets on a Ticket Management tool and Asset Management Systems such as BMC Remedy / HP IT Service Manager / Service Now

Competitive Advantage
  • Prior experience in Banking/Financial Service industry
  • White glove customer service
  • Certification (A+, Network+, CCNA, MCSA)
]]>
Wed, 18 Jul 2018 00:00:00 PDT 0
<![CDATA[Scientist I]]> Bayside Solutions is seeking a Scientist I to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Scientist I

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • DMPK department is seeking for a candidate for an Associate Scientist position.
  • The position will primarily support new modality drug discovery within the bioanalysis group.
  • This role will also be involve in new assay development and exploration of novel analytical tools to address DMPK challenges.

Summary of Qualifications:
  • PhD in analytical chemistry or biochemistry discipline is required.
  • Experience in mass spectrometry analysis of peptides, nucleic acids, proteins or glycans is a must.
  • Experience with bioanalysis preferred.
  • Experience with biochemical purification is a plus.
]]>
Mon, 16 Jul 2018 00:00:00 PDT 0
<![CDATA[Sr Software Engineer (Site Reliability)]]> Client Industry: Health care IT

Location: San Diego, CA / Campbell, CA

Position: Senior Site Reliability Engineer

Duration: 6-12 months contract to hire

 

Summary:

Our client works in a high-pace and extremely collaborative Agile environment, thus the ability to engage your peers to propose, express and challenge ideas is extremely important. Emphasis is laid on the creation and self-maintenance of documentation, so clarity in the candidate’ s ability to express ideas and concepts is required.                        

We are seeking a Senior Site Reliability Engineer to work with the software engineering teams at our client’ s site to ensure that compilation, assembly, and delivery of their source code is executed with precision. This role will maintain services in the engineering environment once they are live by measuring and monitoring availability, latency and overall system health. This is a contract to hire role.

Overall competency areas:

Builds Trust: You honor your word by doing what you say you are going to do. 

Implementation/Execution: You are good at organizing and managing multiple priorities and/or projects by using appropriate methodologies and tools. 

Innovate: You introduce new ideas and processes that improve performance and productivity.

Problem Solving: You are a problem solver with the ability to encourage others in collaborative problem solving. Acting as both a broker and consultant regarding resources, you engage others in problem solving without taking over.   

Must Have Skills:
  • 10 years’ experience - at least 5 years as a Site Reliability/DevOps Engineer and 5 years minimum software development industry experience is required
  • Strong knowledge of source code repository administration (git), build setup and administration (Jenkins and Jenkins Job DSL) and superior experience utilizing software build/configuration tools such as Maven and Gradle is essential.
  • Experience with automation of scripts.
  • Daily maintenance of source repositories.
  • Proficiency in Linux.
  • Distributed deployment and install of releases to single/multiple-host environment.
  • Expertise in analyzing and troubleshooting large-scale distributed systems (Micro Services).
  • Automated Build implementation using Jenkins.
  • Proficiency in Jenkins Job DSL (or Jenkins 2.0).
  • Proficiency in code quality tools such as SonarQube or similar.
  • Proficiency in Docker.
  • Proficiency in build repository tools such as Artifactory or similar.
  • Proficiency in automated deployment tools such as Kubernetes or similar.
  • Git and GitHub Source Control - Branching / Merging / Tagging.
  • Effective communication with other teams and co-workers.
  • Systematic problem-solving approach, combined with strong communication skills and a sense of ownership and drive.
  • Ability to identify and communicate code metrics (quality, performance, security, etc.) identified in the build process.       
  • Ability to coordinate and work with other Site Reliability Engineers in local and remote offices.

Desired Skills:
  • Experience with agile based iterative development (Scrum) and knowledge of software engineering best practices
  • Java programming experience.
  • Proficiency in shell scripting.
  • Proficient with Virtualization technologies such as AWS.
  • Knowledge of JIRA and Confluence.
  • Experience with Chef, Puppet, or any other software configuration management tool is a huge plus.
  • iOS Mobile build experience.

Education: Bachelor’ s Degree or above (Computer Science, Bio Engineering, Electronics and Electrical Engineering or any related field)

 

 
]]>
Mon, 16 Jul 2018 00:00:00 PDT 1
<![CDATA[Software Engineer 2 (Site Reliability)]]> Client Industry: Health care IT

Location: San Diego, CA / Campbell, CA

Position: Site Reliability Engineer

Duration: 6-12 months contract to hire

Summary:

Our client works in a high-pace and extremely collaborative Agile environment, thus the ability to engage your peers to propose, express and challenge ideas is extremely important. Emphasis is laid on the creation and self-maintenance of documentation, so clarity in the candidate’ s ability to express ideas and concepts is required.

We are seeking a Site Reliability Engineer to work with the software engineering teams at our client’ s site to ensure that compilation, assembly, and delivery of their source code is executed with precision. This role will maintain services in the engineering environment once they are live by measuring and monitoring availability, latency and overall system health. This is a contract to hire role.

Overall competency areas:

Builds Trust: You honor your word by doing what you say you are going to do. 

Implementation/Execution: You are good at organizing and managing multiple priorities and/or projects by using appropriate methodologies and tools. 

Innovate: You introduce new ideas and processes that improve performance and productivity.

Problem Solving: You are a problem solver with the ability to encourage others in collaborative problem solving. Acting as both a broker and consultant regarding resources, you engage others in problem solving without taking over.   

Must Have Skills:
  • 7 years’ experience - at least 2 years as a Site Reliability/DevOps Engineer and 5 years minimum software development industry experience is required
  • Strong knowledge of source code repository administration (git), build setup and administration (Jenkins and Jenkins Job DSL) and superior experience utilizing software build/configuration tools such as Maven and Gradle is essential.
  • Experience with automation of scripts.
  • Daily maintenance of source repositories.
  • Proficiency in Linux.
  • Distributed deployment and install of releases to single/multiple-host environment.
  • Expertise in analyzing and troubleshooting large-scale distributed systems (Micro Services).
  • Automated Build implementation using Jenkins.
  • Proficiency in Jenkins Job DSL (or Jenkins 2.0).
  • Proficiency in code quality tools such as SonarQube or similar.
  • Proficiency in Docker.
  • Proficiency in build repository tools such as Artifactory or similar.
  • Proficiency in automated deployment tools such as Kubernetes or similar.
  • Git and GitHub Source Control - Branching / Merging / Tagging.
  • Effective communication with other teams and co-workers.
  • Systematic problem-solving approach, combined with strong communication skills and a sense of ownership and drive.
  • Ability to identify and communicate code metrics (quality, performance, security, etc.) identified in the build process.       
  • Ability to coordinate and work with other Site Reliability Engineers in local and remote offices.

Desired Skills:
  • Experience with agile based iterative development (Scrum) and knowledge of software engineering best practices
  • Java programming experience.
  • Proficiency in shell scripting.
  • Proficient with Virtualization technologies such as AWS.
  • Knowledge of JIRA and Confluence.
  • Experience with Chef, Puppet, or any other software configuration management tool is a huge plus.
  • iOS Mobile build experience.

Education: Bachelor’ s Degree or above (Computer Science, Bio Engineering, Electronics and Electrical Engineering or any related field)

 
]]>
Mon, 16 Jul 2018 00:00:00 PDT 1
<![CDATA[Process Engineer]]> Bayside Solutions is seeking a Process Engineer  to be a part of our partner’ s team in the South Bay  area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Process Engineer

Job Benefits:
  • An opportunity to join a genomics sequencing organization. 
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Support quality compliance, MFG system test, and design/process improvement projects.
  • Executing failure analysis investigations, risk impact assessment and root cause investigations.
  • Generating technical documents, including IQ/OQ/PQ, SOPs, URS, Design and Functional Specification, Executed FAT and Site Acceptance Testing (SAT) verification, as well as final reports.
  • Collaborate with design engineers in generating product configuration documentation, including specification and assembly drawings and BOMs.
  • Support the coordination between internal and external resources for product transfer.
  • Develop and document new methods and procedures for production processes.

Required Qualifications:
  • B.S. in Engineering, Mechanical, Electrical, Chemical, or related field with minimum 5 years of experience.
  • Experience with lab equipment and instruments involving liquid and gases.
  • Design experience including but not limited to pneumatic and electric actuators, solenoid and pneumatics valves, fixture and tooling using Solid Work, high precision tolerances components and assemblies.
  • Hands-on experience on fluid and pneumatics circuits from schematics readings, P&ID’ s troubleshooting, components assembly and testing including microcontroller and basic PLC knowledge.
  • Prefer experience with statistical data analysis using JMP.
  • Prefer familiarity with board schematics, BOMs and test instrumentations.
  • Experience using automated inspection instruments.
  • Capable in generating part and assembly drawings in Solidworks. 
  • Good written and verbal communication and presentation skills.
  • Strong attention to detail, accuracy and completeness of data, reports, records, etc.
  • Creative problem solving skills.
  • Good organizational and planning skills.
  • Ability to work independently and with others as a team. 
  • Able to travel local and overseas.
]]>
Fri, 13 Jul 2018 00:00:00 PDT 0
<![CDATA[Project Coordinator]]> Bayside Solutions is seeking a Project Coordinator to be part of our client’ s team in Los Gatos. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Project Coordinator:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Coordinates project planning and implementation, including assessing needs and objectives.
  • Participates in program or project budget planning and development.
  • Establishes project work plan and calendar or schedules; monitors, reviews, and evaluates progress.
  • Coordinates and attends meetings; creates meeting minutes; establishes and maintains internal and external contacts as necessary.
  • Updates existing Microsoft project timelines Analyzes and prepares program, project and / or budget documents.
  • Monitors record keeping and file maintenance for the program or project.
  • Prepares records of project activities; oversees and ensures the timely processing in and the delivery of required materials.
  • Verifies and analyzes the accuracy of all data and information used or generated by project; resolves any discrepancies or problems.
  • Serves as liaison for department; coordinates activities, follows up on action items and exchanges information.

Summary of Qualifications:
  • Bachelor degree or equivalent years of experience.
  • One year of office experience including or supplemented by project planning and implementation experience.
  • Knowledge of project planning methodologies such as critical path planning.
  • Proficient in Microsoft word, excel and PowerPoint.
  • Knowledge of SharePoint Knowledge of Microsoft Project Excellent communications and leadership skills.
  • Excellent planning and organizational skills Problem solving skills.
  • Ability to accurately review and complete detail oriented information and projects.
  • Ability to conceptualize and organize project planning process.
  • Ability to take responsibility and function under minimal supervision.
  • Ability to work with wide range of people.

 
]]>
Fri, 13 Jul 2018 00:00:00 PDT 0
<![CDATA[Associate Service Engineer]]> Bayside Solutions is seeking a Associate Service Engineer  to be a part of our partner’ s team in the South Bay  area. This is an opportunity to be a part of a passionate team developing and transferring technologies for fast and low-cost genome sequencing.

Our partner’ s culture is ethical, honest and highly collaborative!

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Associate Service Engineer

Job Benefits:
  • An opportunity to join a genomics sequencing organization. 
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Support troubleshooting and preventive maintenance of lab instruments and equipment, heavily used in biochemistry/engineering labs, including next generation DNA sequencing instrument.
  • Draft the hardware engineers’ mechanical designs and drawings.
  • Support hardware development team to design, machine and assemble mechanical/fluidic/optical prototypes.
  • Collaborate with internal and external engineering and scientific groups as needed to ensure an integrated design that meets the system requirements. 
  • Perform other work related duties as assigned.
  • Travel: 10-20 %

  Required Qualifications:
  • BS or MS in mechanical engineering or similar education and 2+ years of related experience.
  • Experience in service and in preventive maintenance of lab instruments and equipment.
  • 2+ years of experience with solid-modeling software (SolidWorks preferred).
  • Solid understanding of engineering fundamentals and analytical methods. 
  • Experience with next generation DNA sequencing instruments.
  • Experience with optomechanical design for sensitive optics in benchtop instruments.
  • Experience with fluidics and automated liquid handling.
  • Experience in assembling complex, precision mechanical systems from concept through production.

 
]]>
Thu, 12 Jul 2018 00:00:00 PDT 0
<![CDATA[Postdoctoral Research Fellow]]> Bayside Solutions is seeking a Postdoctoral Research Fellow  to be a part of our partner’ s team in the South Bay  area. This is an opportunity to be a part of a, passionate team developing and transferring technologies for fast and low-cost genome sequencing.

Our partner’ s culture is ethical, honest and highly collaborative!

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Postdoctoral Research Fellow

Job Benefits:
  • An opportunity to join a genomics sequencing organization.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Work together with a  team of in house technical experts, come up with  ideas and contribute to the execution of the ideas independently and collaboratively. 
  • Perform DNA engineering activities including standard molecular biology enzymatic relations, PCR, qPCR, DNA cloning and sub-cloning, site specific mutagensis, standard or next-gen genomic or cDNA library preparation, vector construction, synthetic biology, and sequencing. 
  • Be self - sufficient on project/activities assigned yet communicate collaboratively within and beyond the project team with concise reports
  • Work  in a fast paced industrial environment. 
  • Facilitate knowledge between California and Shenzhen teams. 
  • Willing to travel if needed. 

Required Qualifications:
  • PhD degrees in the field of life sciences (biology, molecular biology, biochemistry, biophysics, genetics, and bio engineering)
  • Demonstration of success in graduate school (e.g. high quality publications)
  • Must have proficient written, communication, and presentation skills in English. 
  • Mandarin speaking and/or writing is a plus. 
  • Prior industrial experience is a plus. 
]]>
Thu, 12 Jul 2018 00:00:00 PDT 0
<![CDATA[Clinical Trial Leader]]> Bayside Solutions is seeking a Clinical Trial Leader to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Clinical Trial Leader

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Serves as a member of one or more global cross-functional Protocol Execution Team(s) (PETs) through all study stages (start-up, conduct, close-out) to contribute to the accomplishment of studies outlined by the clinical development plan:
  • Participates in developing and finalizing cross-functional activities to ensure delivery of critical clinical trial documents such as informed consent forms (ICFs), protocols, site and country budget templates, EDC, IxRS, central / specialty lab, ECG, imaging, and PRO specifications, drug supply and biomarker / sample management plans, TMF, and CSRs.
  • Liaises with cross-functional team members including the PET members to solicit input.
  • Drafts and implements study plans including; vendor oversight, risk, quality, safety, communication, trial/medical monitoring, TMF.
  • Ensures TMF creation and QC completion.
  • Supports EDC and CTMS systems and data maintenance.
  • Tracks budget, timelines, milestones, and critical study activities, identifies issues and proposes potential resolutions.
  • Provides strategic operational input on protocol feasibility.
  • Provides input to the study budget and manages assigned vendor budget(s); communicates variances in actual versus forecasted spend in vendor budgets and presents an action plan for resolution to Protocol Execution Team Lead (PETL).
  • Participates in selection of vendors (participates in the Request for Proposal (RFP) process), on a global scale, in collaboration with the PETL Utilizes outputs from operational analytical tools to enhance and improve study execution.
  • Oversees delegated outsourced activities to ensure CRO and vendor delivery against contracted scope of work.
  • Contributes to global study site selection & management: Conducts global protocol, country, and site feasibility assessments.
  • Assists with all activities related to global site selection, contracting, set-up and maintenance.
  • Partners with Site Contracts on development of site budget template and budget negotiations.
  • Contributes to the development and active management of study-specific patient recruitment strategies through participation in enrollment planning workshops.
  • Proactively identifies risks and develops risk mitigation strategies to ensure operational effectiveness.
  • Contributes to the efforts and overall success of the wider gRED Clinical Operations team: Collaborates effectively and participates in the CTL Forum and other departmental meetings.
  • Identifies and synthesizes best practices and process improvements and shares outputs with peers.
  • Coordinates planning and execution of effective investigator meetings.
  • May be accountable for driving agenda and content for investigator meetings.
  • Stays current on relevant therapeutic knowledge and clinical research best practices.
  • Ensures accuracy and timeliness of CTMS, timeline planning tools and other core systems.
  • Ensures study adherence to ICH/GCP and SOPs.

Summary of Qualifications:
  • Bachelor' s degree or equivalent required (scientific or healthcare discipline preferred). 7+ years of study management experience in clinical and drug development.
  • Working knowledge of GCP/ICH requirements, international regulatory guidelines, and the drug development process.
  • Other (e.g. Travel): Willingness to travel domestically.
  • Work on nights or weekends is not typically required, however, interaction on global clinical studies requires flexibility for occasional teleconferences / meetings outside of core working hours.
  • Experienced in managing aspects of one or more early development phase (I and II), global, complex, clinical studies and generally experienced in clinical research/development.
  • Demonstrated experience in at least one therapeutic area.
  • Experience with effective vendor management.
  • Strong customer focus with investigators, functional peers, vendors, country affiliates, etc.
  • Strong technical and analytical skills and ability to manage system data maintenance across multiple systems.
]]>
Wed, 11 Jul 2018 00:00:00 PDT 0
<![CDATA[Biosample Operations Lab Technician I]]> Bayside Solutions is seeking a Biosample Operations Lab Technician I to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Biosample Operations Lab Technician I:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Performs manual and/or automated sample processing for serum/plasma/urine/DNA/RNA aliquoting.
  • Performs DNA/RNA isolation from various clinical sample types (Blood, Tissues, WBCs, plasma, saliva, urine) on a routine basis, according to timelines set by the Supervisor.
  • Performs in-process QC methods to assess quality of samples.
  • Maintains detailed laboratory records of samples QC steps and related quality data.
  • Supports the evaluation of novel technologies and techniques for their suitability for analyzing clinical samples.
  • Supports method development, qualification, and implementation of laboratory instruments.
  • Supports laboratory process optimization and validation.
  • Support experiments that address critical findings from analytical data anomalies that are potentially sample-related; participates in interpretation of results and authorship of final reports.

Summary of Qualifications:
  • BS Degree in science and 3 years of lab experience handling biological samples and experience in Molecular Biology techniques required.
  • MS with > 3 years of hands-on experience handling biological samples and Molecular Biology techniques in a Pharma/Biotechnology or academic labs preferred. 
  • Demonstrated experience working in a laboratory managing clinical or non-clinical samples.
  • Demonstrated experience in molecular techniques including DNA/RNA extraction, Picogreen & Ribogreen quantitation, PCR, RT-PCR.
  • Experience in utilizing a variety of analytical platforms and instrumentation.
  • Proficiency with PC computer systems, including email and calendar applications and MS Office.
  • Good organizational, multitasking, and prioritization skills.
  • Good written and oral communication skills.
  • Requires attention to detail, and accuracy in data entry, while maintaining study timelines.
  • Good analytical and problem solving skills, paired with partnering and performance skills.
  • Team player with demonstrated good interpersonal skills and an ability to build effective working relationships within functional area.
  • Demonstrated ability to work under pressure and to tight timelines.
  • Customer orientated mind-set.
  • Good level of initiative and the ability to work independently and with minimal supervision. 
  • Experience with Micro Array, NGS and WGS.
  • Working knowledge of laboratory functions (ex. LIS, LIMS, Quality, etc.).
  • Computer skills in laboratory informatics systems and data processing.
  • Experience working in multi-cultural teams.
]]>
Wed, 11 Jul 2018 00:00:00 PDT 0
<![CDATA[Sr. Specialist, Quality Complaints]]> Bayside Solutions is seeking a Sr. Specialist, Quality Complaints to be part of our client’ s team in East Bay Area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Sr. Specialist, Quality Complaints:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Responsible for oversight of the Fremont Product Complaint process:
  • Development and maintenance of all SOPs related to Product Complaint process
  • Tracks, monitors and reports related metrics/KPIs
  • Product Complaint record trending and analysis
  • Partners with internal stakeholders and BI Network to drive consistency and continuous improvement of quality systems
  • Fremont Site Complaint Officer:
  • Investigate product complaints reported for and Client based products
  • Coordinate investigative activities with internal SMEs and external lab/facilities
  • Key User/Point of Contact for system used to record and track complaint records (TrackWise)
  • Communication with End Users in support of timely Complaint related activity completion
  • Develop and provide process and system training for site staff involved with the Product Complaints process
  • Directly interfaces with customers and may interact with regulatory agencies regarding BI Fremont' s quality systems, procedures and documentation.
  • Maintains current knowledge of the regulatory environment and requirements regarding GMP Quality Systems in the pharmaceutical/medical device industry. Continuously ensures Quality System processes incorporate updated information and industry learning trends.
  • General Quality System responsibilities:
  • Support maintenance of site investigation and CAPA process, in alignment with site Deviation/CAPA process owner
  • Communication with Deviation, CAPA and Investigation End Users in support of timely Complaint related activity completion
  • Support of KPI and trend analysis as well as report creation for Deviation/CAPA Process
  • Develop and deliver training for Complaint, Deviation, CAPA and Investigation related processes and systems
  • Proactively leads initiatives to improve quality systems in the organization, develops SOPs and KPIs for the business
  • Proactively engages the site to uncover issues and concerns relating to quality systems, and facilitates resolution and continuous improvement
  • Participates in inspection readiness activities
  • May perform Quality risk assessments
  • May cross-train in other disciplines within Quality
  • Participates in and lends expertise to Fremont projects and operational excellence improvement efforts
  • Identifies, designs, and implements process and system improvements
  • Serves as the Quality representative on cross-functional and multi-site project teams
  • Represents Quality in cross-functional meetings, provides subject matter expertise, and makes sound decisions

Summary of Qualifications:
  • Bachelor' s degree required in a relevant discipline; advanced degree preferred.
  • Minimum eight years of general experience in the pharmaceutical industry with direct experience in a cGMP manufacturing environment
  • Minimum five years’ experience in a cGMP manufacturing, quality systems or process/continuous improvement role required
  • Comprehensive knowledge and understanding of regulatory requirements as governed by cGMP and regulatory agencies (FDA, EMA, TGA)
  • Strong proficiency with TrackWise or related Quality System applications.
  • Strong facilitation skills
  • Demonstrated history of successful development and implementation of robust quality systems and processes
  • Proven ability to work creatively and analytically in a problem-solving and process-oriented environment.
  • Proven ability to work in a collaborative, team-based environment dependent upon effective teamwork to achieve goals and company objectives.
  • Excellent leadership, communication (written and oral) and interpersonal skills required.
  • Proficiency in the use of Microsoft Office Software (Word, Excel, PowerPoint, Visio, Access, Project).
  • Six Sigma and/or Lean experience preferred
  • Proficiency in the use of Microsoft SharePoint

 
]]>
Wed, 11 Jul 2018 00:00:00 PDT 0
<![CDATA[Scientist I]]> Bayside Solutions is seeking a Scientist I to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Scientist I

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • The Pharmacometrics Scientist is responsible for the Pharmacometrics (PMx) strategy for his/her development project[s] in order to ensure that appropriate dose/route/schedule decisions are made for the patients.
  • The PMx Scientist uses state of the art model-informed drug development strategies that are aligned with project needs.
  • The PMx Scientist works in close partnership with Clinical Pharmacologists, Biostatisticians, Clinicians and cross-functional project teams.
  • The responsibility for the Associate PMx Scientist is to perform population PK/PD models, translational models, disease models, exposure-response models, biomarker-efficacy models, clinical trial simulations, literature meta-analysis, and other state of the art modeling and simulation techniques.
  • Based on experience and ability, the PMx Associate Scientist may also develop and/or lead the implementation of the Modeling and Simulation strategy for a disease area or project, represent PMx on cross-functional project teams.
  • Other responsibilities may include contribution to department initiatives, or other duties as assigned.

Summary of Qualifications:
  • MD, PhD, PharmD or equivalent in Pharmacokinetics, Pharmaceutical Sciences, Biomedical Engineering or related quantitative discipline.
  • Familiarity with quantitative approaches in drug development, working knowledge of relevant modeling software (e.g. NONMEM, ADAPTII, Monolix, Matlab, R).
  • Based on experience and ability, the PMx Associate Scientist may lead CP teams and represent CP on cross-functional teams. 
  • Experience/knowledge of how Clinical Pharmacology (CP) science can impact drug development is preferred. The PMx Associate Scientist requires good communication skills, both written and oral.
  • Working knowledge of PK/PD data analyses, statistical approaches as they apply to clinical study design & analysis, familiarity with clinical study design options and/or working knowledge of relevant disease areas is preferred.
]]>
Tue, 10 Jul 2018 00:00:00 PDT 0
<![CDATA[Research Associate]]> Bayside Solutions is seeking a Research Associate to be part of our Client’ s team in San Francisco. This is an opportunity to work with a local Biopharmaceutical start up company, who focus on developing oncology therapeutics across a broad range of tumor types. 

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize consumable devices that enable leading-edge medical research.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • We are seeking a highly motivated research associate to study novel oncology mechanisms using first in class small molecule drugs.
  • You will be responsible for driving our in vitro experimental efforts in close collaboration with our academic and corporate partners.
  • You will use your lab based expertise in cell and molecular biology to investigate key target biology mechanisms and test the effects of our novel drugs at both the cellular and molecular level.
  • The successful candidate will be highly proficient at in vitro, cell based experimentation and bring an innovative approach to the lab. 
  • The job will include experimental design, execution, data analysis and presentation of data. 

Job Qualifications:
  • Bachelor’ s degree with 2-4 years of scientific experience in the biopharmaceutical industry or a Master’ s degree with 1-2 years of experience.
  • Degree in Cellular Biology, Pharmacology or a related field is essential.
  • Experience conducting and developing quantitative human cell-based assays is required.
  • Experience with flow cytometry and immune-assays is required.
  • Creativity and the ability to work within a collaborative team with outside academic and corporate partners to achieve technical and corporate milestones.
  • Exceptional communication, critical thinking, and problem-solving skills.
  • Ability to rapidly learn and apply techniques.
]]>
Tue, 10 Jul 2018 00:00:00 PDT 0
<![CDATA[Documentation Specialist I]]> Bayside Solutions is seeking a Documentation Specialist I to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Documentation Specialist I

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Participates in site and/or regional PD Disclosures departmental meetings.
  • Operates within a global organization with flexibility for early meetings (1-2 times per week).
  • Represents Disclosures and supports effective and efficient cross-functional PDR coordination, appropriate resources, and timely, thorough and compliant execution.
  • As assigned, may act as a standing or ad hoc member of other teams for special or ongoing initiatives and projects.
  • Participates in site and/or regional PD Disclosures departmental meetings.
  • Operates within a global organization with flexibility for early meetings (1-2 times per week).
  • Represents Disclosures and supports effective and efficient cross-functional PDR coordination, appropriate resources, and timely, thorough and compliant execution.
  • As assigned, may act as a standing or ad hoc member of other teams for special or ongoing initiatives and projects.
  • Continues to expand his/her knowledge base of laws, regulations and guidelines governing the development, licensure and marketing of drugs and biologics.
  • Obtains and applies in-depth knowledge of the client and regulatory guidelines, procedures and best practices.
  • As needed, provides Disclosures expertise to cross-functional teams and other groups.
  • Contributes to development and maintenance of policies and/or Standard Operating Procedures (SOPs) on clinical trial registry and clinical trial results database processes.
  • Identifies studies required for registry and results postings, including applicable trials for results postings on relevant external websites.  Ensures that responsible PDR management and staff are aware of timelines, deadlines and other requirements.
  • Tracks missing/late registry entries and Clinical Study Reports (CSRs) and liaises with PDR teams regarding dates of new product or line extension approvals.
  • Liaises with project teams and affiliates to ensure they understand their responsibilities in relation to regulatory documentation disclosures.
  • Submits protocol documents for preparation of registry entry and for quality control checks, i.e., consistency between registry and protocol, cross-protocol and franchise consistency.  Similarly submits CSR document for preparation of results entries.
  • Works with cross-functional team members to obtain data, reviews and approvals required for completion of registry and results entries on internal and external websites.
  • Monitors workflows for registry and results entries to ensure timely and on-target completion.
  • Completes document and data uploads in applicable systems.
  • Ensures protocol information is included in the registry as soon as the study design is finalized and first ethical/regulatory approval is received.
  • Ensures that study results are uploaded into results databases within applicable timeframes.
  • Tracks correspondence with cross-functional teams and departments via departmental mailboxes and ensures appropriate responses are provided in a timely manner.

Summary of Qualifications:
  • Bachelor’ s Degree preferred (life sciences disciplines strongly preferred).
  • Average of 3 or more years’ relevant experience in the pharmaceutical/biotechnology industry. Some previous experience in regulatory affairs or other product development functions is preferred.
  • Medical writing and/or editing experience is preferred.
  • Some understanding of international regulations, processes and issues in drug/biologics development is preferred. Includes GxP (Good Practices for quality guidelines and practices in the pharmaceutical/biotechnology or related industry), GCP (Good Clinical Practice), ICH (International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use), FDA, EMEA, NICE and other relevant guidelines.
  • Has working knowledge of the multidisciplinary functions involved in pharmaceutical/biotechnology product development, e.g. clinical development, clinical operations, biostatistics, commercial operations, etc.
  • Strong computer skills, including Microsoft Office Suite (Word, PowerPoint and Excel) and Adobe Acrobat.
  • Fluent English and other language skills as needed.
  • Some understanding of product and safety profiles.
  • Good negotiation skills: knows how to complete deliverables by working effectively with others internally and externally.
  • Excellent project management skills: can prioritize multiple tasks and goals to ensure the timely, on-target and within-budget accomplishment of such.
  • Good business presentation skills: is comfortable and effective when presenting to others, internally or externally.
  • Good judgment and decision-making skills: knows how to make trade-off decisions while balancing ethics and efficacy.
  • Works well within teams and is effective in collaborating with others internally and externally.
  • Ability to travel as needed.
]]>
Mon, 09 Jul 2018 00:00:00 PDT 0
<![CDATA[Systems Logistics Support Specialist I/II]]> Bayside Solutions is seeking a Systems Logistics Support Specialist I/II to be part of our client’ s team in the Tri-Valley. This is an opportunity to work with a nanopore based DNA sequencing company dedicated to making genetic testing easy and affordable. They are developing a revolutionary, low cost, and semiconductor based DNA/RNA reador. This technology will improve the lives of people with a wide variety of applications including the timely screening of newborns for diseases and the diagnosis of cancers and infectious diseases.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. They take pride in strong, global relationships with the patient, research and medical communities, and take equal pride in carefully selecting their colleagues.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Systems Logistics Support Specialist I/II

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Assist with data entry for the instrument management database (e.g., record instrument activities such as repairs/maintenance, add updated service contract information, and submit requests for changes to instrument status).
  • Assist with management of instrument spare part inventory, e.g., receiving inventory, stocking shelves, tracking inventory levels in the inventory management software tool, and shipping spare parts to engineers at external sites. Lifting required < 20 lbs.
  • Assist with management of reagent and consumable inventory, e.g., receiving inventory, stocking shelves (room temp and cold room), tracking inventory levels, and shipping items to engineers & application specialists at external sites. Lifting required < 20 lbs.
  • Assist with Installation and Operational Qualification (IOQ) documents:  obtain IOQ number from TrackWise, assemble documents for execution, route executed documents for approval, and ship approved documents to Records Management for filing (i.e., tracking IOQ documents from start to finish).
  • Assist with the tracking/management of in-house instrument qualification (IOQ) status in the instrument management database and posting updated signage on the instrument to identify instrument status (e.g., qualified/not qualified).
  • Assist with data entry for equipment non-conformances and exclusions in TrackWise.
  • Coordinate onsite vendor Field Service Engineer (FSE) visits for instrument repairs/maintenance and meet/escort FSE to the labs with the instruments requiring service.
  • Assist with the management of calibrated tools to ensure the tools are submitted for calibration on-time.
  • Assist with the return or disposal of instrument spare parts or computer equipment following internal procedures.
  • Coordinate the printing of training materials and ship to external sites as needed.
  • Provide timely and professional customer support at all times.
  • Be flexible to stop current activities to assist with urgent requests (e.g., shipping packages, preparing/routing IOQ documents).

Required Qualifications:
  • Must have prior experience with data entry.
  • Demonstrated proficiency to learn new skills/software/tools rapidly.
  • Must have strong attention to detail.
  • Must be able to consistently follow instructions/procedures.
  • Must be organized, in order to accommodate changing volume of work.
  • Must be a self-starter and have initiative to ask questions to clarify scope of work.
  • Have excellent communication and customer support skills.
  • Ability to be flexible with changing work priorities and prioritize urgent tasks.
  • Strong work ethic to get tasks done to support team members.
  • Experience with one or more of the following is highly desirable:   SQL database experience, TrackWise, Blue Mountain Regulatory Asset Management database, Experience with Tableau to create reports and dashboards.
  • Knowledge of FDA Quality System Requirements (QSR), In Vitro Diagnostics Directive requirements (IVDD), ISO 13485 is a plus.
]]>
Mon, 09 Jul 2018 00:00:00 PDT 0
<![CDATA[Clinical Safety Associate]]> Bayside Solutions is seeking a Drug Safety Associate I  to be part of our client’ s team in South San Francisco. This is an opportunity to work with one of the largest Biopharmaceutical companies in the world developing innovative medicine to save patients’ lives.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Drug Safety Associate I

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Establishing work priorities and direction independently with minimal input from Manager.
  • Collecting, documenting, and processing adverse event (AE) reports from clinical trials and post-marketing sources in accordance with company Standard Operating Procedures (SOPs) and work practices to ensure and maintain regulatory compliance.
  • This includes detailed review of source documentation, assessing cases for reportability, accurate data entry, and quality check.
  • Preparing clinical narrative summaries independently for AE reports from clinical studies and spontaneous post-marketing reports and formulates follow-up information requests.
  • Performing active follow-up via telephone contact with consumers and health care professionals.
  • Coding all AEs in MedDRA independently.
  • Ensuring timely reporting of SAEs/AEs to Regulatory Authorities, and cross-reporting to pharmaceutical partner(s).
  • Participating in the preparation of aggregate safety reports, such as biannual safety reports to Ethics Committees and annual reports to regulatory authorities.
  • Conducting periodic reconciliation of SAEs between drug safety and clinical trial databases for ongoing clinical studies with little or no supervision.
  • Representing the DSRM department on project teams.
  • Completing individual projects in support of DSRM department initiatives.
  • Working with Clinical Research Department and Contract Research Organizations, sometimes in a lead capacity, regarding information exchange and safety exchange agreements.

Summary of Qualifications:
  • Health care professional degree (PharmD, RN, MD) with at least 2 years drug safety experience AND additional clinical or pharmaceutical experience.
  • Strong verbal and written communication skills demonstrated by the ability to interpret and communicate medical information and write summary reports, if needed.
  • Strong interpersonal skills especially for proactive drug safety representation on clinical/project team and investigator meetings, and communications with contract research organizations (CROs) involved in safety reporting.
  • Candidate must have the ability to organize workflow activities, able to multi-task, be performance-driven, and possess good decision-making skills.
  • Computer literacy including working knowledge of computer applications such as word processing, spreadsheets and electronic mail is required; experience with data entry into drug safety databases strongly desired; ARISg experience a plus.
  • Knowledge of domestic and international drug safety regulations, industry practices and standards as well as clinical knowledge in appropriate therapeutic area is preferred.
]]>
Tue, 03 Jul 2018 00:00:00 PDT 0
<![CDATA[Architect/Planner II ]]> Bayside Solutions is seeking an Architect/Planner II  to be part of our client’ s team in South San Francisco. This is an opportunity to work with one of the largest Biopharmaceutical companies in the world developing innovative medicine to improve the quality of patients’ lives.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Architect/Planner II

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation. 
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • The Occupancy Planner will partner with the Scenario & Space Planning Team as well as other Workplace Effectiveness & Site Services Teams to support the campus occupancy plan. Responsibilities:
  • Partner with S&SP Team on Occupancy Planning & related activities, including:
  • Scenario planning, option development, and Stack planning.
  • Block planning, including analysis of office/cube ratios.
  • Neighborhood planning monitoring day-to-day space utilization Adjacency mapping.
  • Migration planning supply/demand summaries Detailed move planning of all group moves (greater than 10 people).
  • Quarterly alignment on headcount growth, including working with S&SP Team client validation, executive summaries, detailed scenario charts & graphs etc.
  • Assist with executive presentations on occupancy planning studies, 5-year occupancy plan, 5-year amenities plan, NWE (Neighborhood Work Environments) Pipeline & Governance, etc.
  • Conduct periodic occupancy audits to ensure information pertaining to department locations, individuals and configuration of spaces are accurate and up to date in CAFM system.
  • Ensure any room-use changes are documented and submitted to the CAFM team Responsible to submit drafting orders (‘ GDO’) to the documentation group for floor plan updates (cubicle and office layouts).
  • Manage allocation planning information into the CAFM system and ensure data is kept up to date Manage space contact information in the CAFM system.

Required Qualifications:
  • Bachelor’ s Degree – Preferred Fields: Architecture, Engineering, Interior Design, Project Management, Construction Management, Business Management, Life Sciences / Research, Strategic Planning, Project Planning, Facilities Management.
  • 2-4 years of experience in Facility Planning, Architecture or Interior Design.
  • Ability to define problems, collect data, establish facts, and draw valid conclusions.
  • Exceptional written and verbal communication skills.
  • Exceptional interpersonal skills to maintain positive internal and external relationships.
  • Proficient in google Apps, PowerPoint, Excel, Word, Adobe, Smart sheets & CAFM/ARCHIBUS; CAD experience a plus.
  • Ability to successfully multitask and able to adjust tasks in accordance with changing deadlines and priorities .
  • Organized, independent and self-motivated (entrepreneurial), enthusiastic, dependable, detail-oriented, flexible in scheduling and prioritization.
]]>
Tue, 03 Jul 2018 00:00:00 PDT 0
<![CDATA[Research Associate III/Scientist I]]> Bayside Solutions is seeking a Research Associate III/Scientist I  to be a part of our partner’ s team in the Newark  area. This is an opportunity to work within a life-changing biotechnology company poised to change the neuromodulator aesthetic and therapeutic product categories.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate III/Scientist I

Job Benefits:
  • An opportunity to join a bio-technology company developing and delivering next-generation neuromodulator, daxibotulinumtoxinA, and highly purified botulinum toxin  type  A.
  • Work for a company that likes to dream and think big! They are local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Assist develop new assays and improve existing methods.
  • Follow SOP and support routine testing.
  • Good communication skill and able to
  • Detail-oriented and excellent organization to multi-task and manage multiple projects.
  • Critical thinking and shows the ability in troubleshooting
  • Self-motivated, fast-learner and able to follow instructions
  • Enjoys working independently under general direction in a fast-paced, multi-tasking environment

Required Qualifications:
  • BS or MS in related scientific discipline with 8+ years industrial experience.
  • PhD in related scientific discipline with 5+ years hand on experience
  • Experience in assay development is a must
  • Solid technical training in general laboratory practices is required (e.g., buffer preparation, sample dilution). Good pipetting skill is essential.
  • Proven in-depth knowledge in protein chemistry
  • Expert in SDS-PAGE, Western Blot and ELISA
  • Mammalian cell culture experience is a plus
  • Experience in CE-SDS is a plus
  • Proficient written and verbal communication skills are required.

Additional Skills:
  • Proficient with Microsoft Word and Excel
  • Ability to work independently and troubleshoot unexpected challenges

 
]]>
Tue, 03 Jul 2018 00:00:00 PDT 0
<![CDATA[Sr. Recruiter]]> Bayside Solutions is seeking a Sr. Recruiter to be part of our client’ s team in the Tri-Valley. This is an opportunity to work with the largest biotech company and deliver better-targeted therapies

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Sr. Recruiter

Summary of Responsibilities
  • Manages the full-cycle recruiting process to include: developing and implementing sourcing strategies, review resumes and conduct interviews (pre-screening), with key emphasis on pipeline development and improving time to fill.
  • Proactively networks and establishes effective working relationships Maintains a high level of customer service by partnering with all levels of management in order to make successful hiring decisions.
  • Previous experience recruiting in the  Life Sciences  industry and successful  hiring of  Clinical/Scientific candidates is highly preferred.
  • Communicates progress to goals to the Talent Acquisition Lead/Manager/Director, HR Business Partner, and internal customer groups. Completes all reports associated with status updates and compliance.
  • Partners with Hiring Managers/functional Human Resources in order to identify, communicate, and achieve Affirmative Action goals/targets.
  • Identifies and pursues cost-containment efforts in recruiting, continually seek new sourcing options, and develop creative approaches to delivering candidates to the customer.
  • Tracks all internal and external applicants and ensures all job postings meet requirements of EEO/AA compliance guidelines.
  • Ensures compliance with all hiring practices, as outlined by client’ s policy and procedures and EEO/AA compliance guidelines.
  • Ensures candidate(s) status in company' s ATS (Workday) and all candidate tracking logistics are properly maintained.
  • Performs miscellaneous duties and special projects in support of the HR department, as assigned.

 Required Qualifications
  • Bachelor’ s degree and/or equivalent education and experience.
  • Requires a minimum of 6 years of related experience, of which 4 years must be in recruiting/staffing with a proven track record to fill a variety of different industries, roles, and levels including middle to senior level positions.
  • Experience in corporate recruiting environment highly preferred.
  • Experience with all facets of recruiting, including full cycle recruiting (sourcing, pre-screening, interviews, offer negotiation, closing candidate(s), etc.).
  • Past experience supporting remote managers in multiple locations strongly preferred.
  • Ability to travel up to 25% (local/domestic) to multiple locations, as needed, to support the business needs.

 
]]>
Tue, 03 Jul 2018 00:00:00 PDT 0
<![CDATA[Lab Technician]]> Bayside Solutions is seeking a Lab Technician  to be part of our client’ s team in the East Bay. This is an opportunity to work with a growing biotech startup!

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Lab Technician

Job Benefits:
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary  of Responsibilities:  
  • Prepare necessary materials for experiments using wet lab techniques.
  • Follow appropriate safety procedures while handling potentially hazardous chemicals.
  • Work in clean room and small scale assembly lab environments while adhering to PPE requirements.
  • Ensure labs have necessary supplies to run experiments, which includes chemical surface preparation of materials and assembling small parts.
  • Track reagents and materials used in experiments and assemblies.
  • Keep inventory of supplies and ensure a healthy stock of materials at all times
  • Certify incoming material is inspected and meets known standards.
  • Assist lab personnel with miscellaneous needs.
  • Troubleshoot issues regarding equipment preparation as they arise.
  • Prepare qPCR reagents daily.

Required Qualifications
  •   Bachelor' s Degree, 1 year of experience
  •   Background in molecular biology, biology, microbiology, biochemistry, or similar, or industry experience working with qPCR.
  • Extensive experience with qPCR, PCR, qRTPCR, RT-PCR.
  • Meticulous attention to detail.
  • Ability to follow written and verbal instructions.
  • Willingness to help other lab members.
]]>
Tue, 03 Jul 2018 00:00:00 PDT 0
<![CDATA[Business Analyst I]]> Bayside Solutions is seeking a Business Analyst I to be part of our client’ s team in South San Francisco. This is an opportunity to work with one of the largest Biopharmaceutical companies in the world developing innovative medicine to improve the quality of patients’ lives.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Business Analyst I

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Gather user requirements for Tableau dashboards
  • Provide users with reports on a regular or as needed basis (e.g. SAP Training Reports)
  • Support ad-hoc data or reporting needs through Excel, Google Sheets, Tableau, etc.
  • Maintain and update EHS website. Support migration of website from HTML to Wordpress.
  • Coordinate software upgrades on a regular basis by communicating and working with software vendors and the IT department.
  • Work with users to optimize existing spreadsheets and Google Sheets or other processes.
  • Develop Google Scripts to create and/or enhance functionality of Google Sheets and Google Forms which support EHS programs.
  • Query SQL and Oracle databases to provide data to users and to troubleshoot data issues.
  • Work with PharmaInformatics (IT) to resolve software related issues.

Required Qualifications:
  • A bachelor’ s degree is required. A degree in engineering, computer science or related technical field is highly preferred.
  • Minimum of 3 years of relevant working industry experience.
  • Experience with development of Tableau dashboards with connections to various data sources (Third-party databases, Excel, Google Sheets, etc.)
  • Exceptional analytical and conceptual thinking skills.
  • Excellent communication skills with the ability to influence stakeholders and work with them to understand their needs and develop acceptable solutions.
  • Ability to generate queries to interact with Oracle and SQL databases.
  • Competency in Microsoft Word, Excel, and Powerpoint.
  • Familiarity with the entire Google Suite of applications (Sites, Sheets, Slides, Forms, Docs, Scripts, etc.)
  • Excellent documentation skills and.
  • Experience creating detailed reports that are easily understood by the user/customer.
]]>
Fri, 29 Jun 2018 00:00:00 PDT 0
<![CDATA[Manufacturing Associate]]> Bayside Solutions is seeking a Manufacturing Associate, to be part of our client’ s team in San Francisco. This is an opportunity to work with a great Biotechnology company committed to the development and commercialization of innovative new gene therapy treatments for people with serious rare diseases. Gene therapy technology has tremendous potential as a treatment approach for many genetic diseases.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. They take pride in strong, global relationships with the patient, research and medical communities, and take equal pride in carefully selecting their colleagues.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Manufacturing Associate

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Perform all manufacturing operations under cGMP/ISO requirements.
  • Adhere to valid manufacturing procedures and documentation.
  • Collaborate with process development, support process development experiments.
  • Perform legible, clear, and concise data entry into batch records, logbooks, and all other ancillary controlled forms used in a cGMP process.
  • Contribute technical writing for SOPs and Batch Records.
  • Maintain a high level of quality and compliance with regards to all aspects of manufacturing.
  • Operate production equipment, including inspection, set up, processing, and cleaning.
  • Attend safety meetings and follow all safety procedures as defined, including maintaining a safe work environment for both self and colleagues.
  • Identify and communicate issues to Manufacturing Supervisor and/or other manufacturing support personnel.
  • Execute corrective measures addressing any issues in a timely manner.
  • Contribute to process improvement plans and implementation of such plans.

Required Qualifications:
  • B.S. in Science or Engineering or equivalent experience such as 3 years' experience in the pharmaceutical or biotech industry.
  • 1-2 years working in a GMP manufacturing environment in upstream operations.
  • Regulatory knowledge.
  • Experience with single use technologies such as bioreactors, welders, sealers.
  • Strong computer skills including MS Office (Word, Excel).
  • Strong communicator with ability to work independently and as part of a team.
  • Experience in maintaining detailed records Technical understanding of a biotech manufacturing facility.

 
]]>
Fri, 29 Jun 2018 00:00:00 PDT 0
<![CDATA[Sr. Lab Support Coordinator]]> Bayside Solutions is seeking a Sr. Lab Support Coordinator to be part of our client’ s team in the South Bay. This is an opportunity to work with a nanopore based DNA sequencing company dedicated to making genetic testing easy and affordable. They are developing a revolutionary, low cost, and semiconductor based DNA/RNA reador. This technology will improve the lives of people with a wide variety of applications including the timely screening of newborns for diseases and the diagnosis of cancers and infectious diseases.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. They take pride in strong, global relationships with the patient, research and medical communities, and take equal pride in carefully selecting their colleagues.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Sr. Lab Support Coordinator

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Responsible for coordination of work processes and operation of RSS-Pleasanton Research, Development and Clinical laboratory areas.
  • Maintain lab areas to ensure Quality System compliance, Safety Compliance, and proper equipment management.
  • Manage and support designated laboratory areas by engineers and scientists.
  • Support the Quality Management team in the SOP gaps and present findings for resolution to prepare for the IVD transition.
  • Generate in-house SOPs for programs, devices and projects.
  • Coordinate with System Support Engineers, Facilities, IT, Quality and Safety to ensure laboratory compliance for ISO 13485 and ISO 17035.
  • Train and document orientations for new lab users on laboratory organization, workflows, Quality System compliance, SOPs and Safety requirements.
  • Enforce Safety and other required laboratory practices, with the independent authority to deny lab users room access, impose re-orientation, and contact user’ s supervisor if necessary.
  • Ensure all lab supplies available when needed. Manage inventory through forecasting activities, placing purchasing orders, receiving activities, and physical inventory tracking.
  • Address laboratory organization/waste/cleanliness issues with laboratory users, General Lab Support, and Facilities to ensure compliance.

Required Qualifications:
  • Bachelor’ s degree in Biological/Life Sciences, Chemistry, Biochemistry or related field, or equivalent combination of education and work-experience.
  • Minimum Experience: 4-6 years of relevant industry experience. Preferred Experience: 7-15 years of experience working in an IVD GMP/ISO regulated environment is preferred.
  • Strong writing and communication skills.
  • Teaching background.
  • Possesses excellent people skills with ability to build effective internal/cross-functional relationships.
  • Strong desire to work in a highly regulated environment, with diligent attention to detail to ensure laboratory areas meet regulatory, safety and departmental requirements.
]]>
Fri, 29 Jun 2018 00:00:00 PDT 0
<![CDATA[Associate Engineer]]>
Bayside Solutions is seeking an Associate Engineer to be part of our client’ s team in the South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Associate Engineer:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • This entry level position is for a Validation Contractor for the Technology Validation group in South San Francisco Production (SSFP). 
  • The candidate will be responsible for supporting validation activities.
  • This includes supporting Periodic Reviews of validated equipment in SSFP, which entails review of change records for validation impact, through the TrackWise system.
  • The Periodic Review will also include review of monitoring data trends and validation lifecycle documents.
  • These reviews will be compiled in a Periodic Review summary report.
  • The contractor will also support revalidation execution on equipment to ensure the equipment has been operating in a validated state, Cleaning Validation activities, New Product Introduction (NPI), and qualification of changes to GMP equipment. 
  • Activities may include but are not limited to protocol generation, execution of protocols, swab and rinse water sampling, data analysis, reviewing worksheets, obtaining batch records and QC results, and summary report authoring.
  • The contractor will be expected to work effectively with customers (System Owner and Technical SME and Quality) to complete these validation activities.
  • Contractor must follow all safe work practices including use of appropriate Personal Protective Equipment and ensure training is up to date. 
  • Standard work hours are Monday through Friday day shift however weekend work or off hour work may be required.

Summary of Qualifications:
  • A B.S. or higher in Chemical, Biochemical or Mechanical Engineering or Science discipline with 3-5 years of relevant experience.
  • The candidate must be highly self-motivated, have excellent organization and communication skills, be willing and able to work independently or as part of a multi-disciplinary team. 
  • Attention to detail is essential for a successful candidate. 
  • Experience in a GMP regulated environment and use of quality systems and processes such as change control and discrepancy/deviation processes is desirable, but not required.

 
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Fri, 29 Jun 2018 00:00:00 PDT 0
<![CDATA[Program Manager]]> Program Manager          

Industry: Financial Service

Duration: Contract to Hire

Location: San Mateo, CA             

Interview Process: Phone, Onsite

 

Join Us

Bayside Solutions is an industry-leading provider of staff augmentation and consulting services. Since 2001, we’ ve built our company around a single concept – relationships. We focus on the people we serve. We’ re straightforward, consistent and 100% accountable. We deliver intelligent solutions that help our clients and candidates thrive.

 

The Role

We are looking for an Experienced Program Manager to manage and oversee our team of PM' s who manage a full range of projects, including the larger and more complex corporate or departmental projects and implementations. Duties also include coordinating the efforts of team members and third-party contractors or consultants to deliver projects according to plan. This person will be the Program Manager tasked with transitioning from the current onsite vendor over the next couple of months and then serving as this person to head up the GDPR (General Data Protection Regulation) program.

 

We Have
  • Influence decision-making, obtain buy-in and negotiate resources, scope, and timelines with Project Sponsors, key stakeholders, and project team members.
  • Lead and motivate teams and ensure projects are delivered with a high degree of quality.
  • Manage contract and consulting resources and ensure compliance with the project budget and Statement of Work.
  • Manage all phases of individual projects to ensure they are completed efficiently and meet the customer’ s requirements.
  • Effectively manage the project scope, budget, and timeline. 
  • Utilize analytical and problem-solving skills, as well as project management and technical knowledge, to assess and resolve project-related obstacles.
  • Analyze and assess project requirements and processes and provide recommendations for improvement.
  • Proactively develop contingency and mitigation plans.
  • Effectively communicate relevant project information to project team members, internal customers, and the management team.
  • Communicate difficult and sensitive information tactfully.
  • Work with impacted departments to identify needs and obtain project resources.

 

You Have
  • Bachelor’ s degree in a related field
  • 5+ years of professional experience in project/program management
  • Ability to establish and maintain effective relationships with management, project team members, internal clients, and consultants
  • Strong ability to persuade at all levels of the organization.
  • Ability to work independently, handle multiple priorities, and solve complex problems
  • Knowledge of waterfall and agile methodologies and tools, and experience managing projects in both
  • Ability to identify and provide solutions for improving current practices

 

Competitive Advantage
  • Prior experience working in a financial service/banking industry.
  • Successfully demonstrated experience leading collaborative project teams on technical projects of varying size and complexity
  • Prior experience working with Projects that are multi-year, multi-million dollar efforts involving the replacement of core business systems and involve process changes to multiple business units.
  • Prior experience with GDPR (General Data Protection Regulation) program.

 

 

 

 
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Fri, 29 Jun 2018 00:00:00 PDT 0
<![CDATA[Project Manager (Staff Role - Camas)]]> Project Manager          

Industry: Financial Service

Duration: Contract to Hire

Location: Camas, WA          

Interview Process: Phone, Onsite

 

Bayside Solutions is seeking an experienced Project Manager to independently manage a full range of projects, including larger and complex corporate or departmental projects and implementations. Duties also include coordinating the efforts of team members and third-party contractors or consultants in order to deliver projects according to plan.

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

 

Responsibilities include:
  • Manage all phases of individual projects to ensure they are completed efficiently and meet the customer’ s requirements. Projects may be multi-year, multi-million dollar efforts involving the replacement of core business systems and involve process changes to multiple business units.
  • Lead and motivate teams and ensure projects are delivered with a high degree of quality.
  • Identify and manage potential risks or issues. Proactively develop contingency and mitigation plans.
  • Utilize analytical and problem-solving skills, as well as project management and technical knowledge, to assess and resolve project-related obstacles.
  • Effectively communicate relevant project information to team members, internal customers, and Management
  • Communicate difficult and sensitive information tactfully.
  • Influence decision-making, obtain buy-in and negotiate resources, scope, and timelines with Project Sponsors, key stakeholders, and project team members.
  • Work with impacted departments to identify needs and obtain project resources.
  • Manage contract and consulting resources and ensure compliance with the project budget and Statement of Work.
  • Analyze and assess project requirements and processes and provide recommendations for improvement.

Qualifications:
  • Bachelor’ s degree and 5+ years of project management experience required; or equivalent combination of education/experience
  • Demonstrated experience leading collaborative project teams on technical projects of varying size and complexity
  • Ability to establish and maintain effective relationships with management, project team members, internal clients, and consultants
  • Strong ability to persuade at all levels of the organization.
  • Ability to work independently, handle multiple priorities, and solve complex problems
  • Excellent oral and written communication skills
  • Knowledge of waterfall and agile methodologies and tools, and experience managing projects in both
  • Ability to identify and provide solutions for improving current practices
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Fri, 29 Jun 2018 00:00:00 PDT 0
<![CDATA[Scientist I/II]]> Bayside Solutions is seeking a Scientist I/II to be part of our client’ s team in the Branchburg, New Jersey. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Scientist I/II

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Works under general supervision, to conduct and monitor laboratory experiments utilizing established and published procedures, and technical and theoretical understanding.
  • Makes recommendations to resolve problems encountered during experimental procedures. 
  • Assumes responsibility for the accuracy, quality, and timeliness of experimental results.
  • Plans and executes own work.
  • Summarizes experimental results, and reviews conclusions with supervisor/project leader.
  • Communicates results of experiments in the form of reports and presentations. Keeps supervisor/project leader informed of project status, particularly of significant findings and results in critical problem areas. 
  • Analyzes experimental data using various data analysis software and/or applying quantitative methods.
  • Forms conclusions, and provides/documents process improvements.
  • Uses technical writing skills to produce reports and documents.  May present findings at internal meeting.
  • Performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g., OSHA).
  • Assumes accountability for own electronic notebook documentation, ensuring experimental methods and results are recorded timely, accurately and consistently, and according to established formats.
  • Participates in routine lab maintenance, lab safety, ISO, and QSR implementation.
  • Organize and manage reagent and material stocks and inventories for project at hand.
  • May troubleshoot issues related to instrumentation.
  • With guidance, analyzes and brainstorms alternative approaches to solve problems and finds solutions. Uses discretion and independent judgment to recommend solutions to basic problems that their individual or team projects.

Summary of Qualifications:
  • Must have a B.S. in Molecular Biology, biochemistry or equivalent field.
  • 1-3 years of relevant experience. Experience in device industry is a plus.
  • Experience in extraction and handling DNA, RNA, and clinical specimen is essential. 
  • Hands on experience with qPCR, RTqPCR,  molecular biology and analytical methods are required.
  • Ability to work independently, organize and resolve basic problems, and critical thinking skills.
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Wed, 27 Jun 2018 00:00:00 PDT 0
<![CDATA[Biomarker Operations Project Manager]]> Bayside Solutions is seeking a Biomarker Operations Project Manager to be part of our client’ s team in the South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

8265987

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Provides biomarker operational expertise and guidance to global Study Management Teams (SMTs).
  • Accountable for planning, coordinating, and overseeing all operational activities required to manage the lifecycle of biomarker samples (including companion diagnostic samples/collection, processing, analysis, data delivery process and final sample disposition).
  • Responsible for collaborating closely with biomarker scientists and Biomarker Operations Program Leaders (BOPLs) to execute biomarker operational strategies, serving as a single point of contact for biomarker operations on multiple SMTs, and with internal and external stakeholders.
  • Develops and maintains effective working relationships with SMT members, with particular focus on the operational team, diagnostic partners, external CRO & Central Lab (for outsourced teams), and external biomarker vendors, where applicable.
  • Builds and maintains effective and efficient high performing biomarker sample* analysis & data delivery.
  • Supports relevant stakeholders in their accountabilities, responsibilities and deliverables to drive decisions on timelines.
  • Responsible for the identification and selection of biomarker vendors in collaboration with the BOPL, biomarker scientist, GPPS and diagnostics/CDx managers; ensuring appropriate cross-functional input is incorporated into the scope of work.
  • Ensure collection, delivery and analysis of biosamples under the highest standards of quality, ethics, and informed consent at study level.

Summary of Qualifications:
  • Bachelors or Master’ s degree within Life Sciences, Medical, or Healthcare is required. A PhD or project management certification is desirable.
  • 3+ years of related professional experience in a clinical research setting, clinical/diagnostic laboratory, or pharmaceutical/biotechnology R&D environment.
  • Good knowledge of ICH GCP Competencies.
  • Must have previous project management skills or experience.
  • Global Vendor Management experience is preferred.
  • Extensive clinical development experience with evidence of working in teams running clinical studies.
  • Pharmaceutical industry experience or experience working as a clinical trial coordinator within a clinical trial setting is a plus.
  • Clinical or biological laboratory experience with evidence of involvement in the processing and/or analysis of biological samples.
  • Critical reasoning skills including the identification and resolution of complex problems.
  • Ability to plan, organize, and demonstrate strong time management skills.
  • Highly flexible working in a fast pace global matrix environment.
  • Proven leadership skills, ability to successfully achieve results within a multi-cultural and geographically diverse team.
  • Ability to working within a team environment and create team culture and promotes team spirit.
  • Professional interpersonal skills, excellent oral/written communication and influencing skills.
  • Detail oriented with the ability to work independently and manage multiple competing priorities.
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Wed, 27 Jun 2018 00:00:00 PDT 0
<![CDATA[Accessioning Clerk I]]> Bayside Solutions is seeking an Accessioning Clerk I to be part of our client’ s team in the San Jose. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Accessioning Clerk I:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Following standard operating procedures to enter orders for high complexity clinical lab tests.
  • For efficient and accurate entry of customer and patient demographic data, clinical information, test request information and physician information.
  • Reviewing, understanding and executing customer-specific requirements for order entry.
  • Work closely with Client Services to resolve and escalate incomplete or unclear order issues.
  • Checking the work of others to ensure order entry accuracy.
  • Providing feedback on work process improvements.
  • Document retention which may include filing, scanning, and retrieval of forms.

Summary of Qualifications:
  • High School Diploma required. College degree preferred.
  • High attention to detail and quality. 
  • Ability to follow laboratory procedures and  must adhere to the laboratory’ s quality control policies. 
  • Demonstrate a strong ability to identify and act on issues within an order that may impact customer satisfaction and test turnaround time. 
  • Must be able to type 45 words per minute with excellent accuracy.
  • Experience using laboratory information systems and proficient in Microsoft Office Suite a plus.
  • Superior people skills and a team player.
  • Must be able to lift 35 lbs.
  • Generally, work hours are  Mon-Fri 12: 00-8: 30PM, but are subject to change, depending on sample volume and other business needs.
  • Minimum 6 months to 1 year of experience in order management, preferably in the clinical laboratory or healthcare industry, medical field, or equivalent.
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Wed, 27 Jun 2018 00:00:00 PDT 0
<![CDATA[Research Associate/Sr. RA]]> Bayside Solutions is seeking a  Research Associate/Sr RA   to be part of our Client’ s team in Redwood City. This is an opportunity to work with a local Biopharmaceutical company focusing on the discovery, development, and commercialization of new therapies to treat the pathologic process of fibrotic disorders. 

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate/Sr RA 

Summary of Responsibilities: 
  • Perform in vivo studies to evaluate anti-cancer efficacy of test agents in tumor mouse models
  • Monitor mice groups enrolled in drug efficacy and mechanism of action studies
  • Perform drug dosing by various routes of administration
  • Monitor in-life study measurements: tumor volume, body weight, tracking overall health condition and survival of mice
  • Entering data in animal management software
  • Availability to work on weekends (rotating schedule)
  • Follow laboratory safety guidelines and practices

Required Qualifications: 
  • BS in Biology or related field with 5+ years of direct experience with mouse syngeneic and/or xenograft tumor models in a commercial vivarium
  • Absolutely Required:  Demonstrated experience with subcutaneous tumor models. And ability to work independently, to perform multiple mouse studies simultaneously and to report study data
  • Experience with orthotopic tumor models is desirable (models of renal cell carcinoma, colorectal cancer and mammary carcinoma)
  • Experience with tasks related to efficacy studies: tumor cell implantation, tumor volume measurement, blood draws (survival and terminal bleed), necropsy and tissue collection and processing
  • Experience with dosing of therapeutic agents by various routes of administration (IP, oral gavage and IV)
  • Excellent organizational skills and ability to collaborate with the scientific team

 
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Tue, 26 Jun 2018 00:00:00 PDT 0
<![CDATA[Document Control Specialist]]> Bayside Solutions is seeking a Document Control Specialist  to be a part of our partner’ s team in the Redwood City Area.

Our partner’ s culture is fast paced and passionate about innovative drug discovery and development.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Document Control Specialist

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Responsible for the implementation and daily operations of the document control system in compliance with ISO 13485: 2016, MDD 93/42/EEC, FDA’ s QSR and related applicable regulations and good documentation practices.
  • Ensure the correct and timely implementation of ECOs per the Change Control Process
  • Maintain all hard-copy master document files and controlled binder locations
  • Maintain all controlled document computer files including security and disaster recovery controls
  • Perform word processing tasks and support ensuring proper compliance with controlled document format, content and usage
  • Maintain Document Control logs (ECO Log, Release Document Log, etc.) to ensure accuracy and current information
  • Maintain part numbering system
  • Assist in training employees to Document Control procedures as needed
  • Ensure integrity of files for the purpose of efficient and timely retrieval of generated records
  • Maintain employee Training records and database
  • Conduct Document Control audits as required
  • Provide support with internal and regulatory audits/inspections as required
  • Assist with the maintenance of the External Document Library
  • Support company goals and objectives, policies and procedures, ISO/MDD requirements, the Quality System Regulation, and other regulatory requirements

Requirements of Qualification: 
  • Minimum of 5 years of experience performing documentation and change control processing and records keeping activities in the medical device regulated industry
  • Proficient in Word, Excel and PowerPoint.
  • Some solid knowledge of ISO 13485: 2016 / FDA’ s QSR regulations and current industry trends as related to medical devices
  • Bachelor’ s degree desirable or equivalent industry experience with associate degree
  • Excellent written and verbal communication skills.
  • Self-Starter, detail oriented, quick learner and creative
  • The person in this position needs to occasionally move about inside the office to access file cabinets, office machinery, etc.

 

 
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Thu, 21 Jun 2018 00:00:00 PDT 0
<![CDATA[Case Manager]]> Bayside Solutions is seeking a Case Manager to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Case Manager

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Provides customer focused reimbursement support to patients, pharmacists, physicians and internal sales force.
  • Educates, informs, and assists patients and providers to navigate through the reimbursement process for the assigned product.
  • Identifies barriers to reimbursement and continually identifies and recommends program efficiencies to the Supervisor to promote high quality of work by Access Solutions/GATCF staff.
  • Identifies and facilitates referrals to alternative coverage options and financial assistance programs for patients who are under insured or require copy assistance.
  • Establishes relationships with appropriate stakeholders including internal & external partners.
  • May conduct necessary benefits, coverage and payer research/investigations to ensure appropriate resources, compliance with payer appeal policies, practices, timelines.
  • Educates, informs and generally assists patients and their families, as well as other related external or internal parties on how to navigate the appeals process.
  • This position may require some travel and flexibility in work shift
  • Periodic mandatory overtime throughout the year is required. This may include, but is not limited to, high referral season, new product or system launches,  enrollment renewals, new line extensions, or  any unexpected surge in volume or backlog situations. 
  • Workdays are M-F, but may include weekends as needed.

Summary of Qualifications:
  • Bachelor’ s degree is preferred.
  • A minimum of 3 years of reimbursement experience preferred.
  • Proficient in all aspects of reimbursement (i.e., benefit investigations, payer reimbursement policies, regulatory and administrative rules.
  • Understands reimbursement/funding resources and how to access these resources.
  • Demonstrates effective problem solving skills and provides excellent customer service.
  • Excellent investigational and analytical skills with a proven ability to communicate effectively in both written and verbal format.
  • Ability to work collaboratively in a team structure and responsibly delegates next steps to appropriate team members.
  • Must be able to work effectively under pressure and prioritize tasks.
  • Must be able to follow written Standard Operating Procedure.
  • Candidate must have excellent knowledge of the managed care industry, including government payers.
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Wed, 20 Jun 2018 00:00:00 PDT 0
<![CDATA[Research Associate II / Senior Research Associate]]> Bayside Solutions is seeking a Research Associate I/II to be part of our Client’ s team in Redwood City. This is an opportunity to work with a local Biopharmaceutical company focusing on the discovery, development, and commercialization of new therapies to treat the pathologic process of fibrotic disorders. 

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate II / Senior Research Associate

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Execute assigned tasks following appropriate laboratory/technical procedures under supervision or independently
  • Make detailed observations, record and analyze data
  • Evaluate and report experimental results to supervisor and colleagues on a routine basis with attention to data quality and reproducibility
  • Learn new laboratory techniques, troubleshoot experiments, and ensure experiments are well designed and performed to a high standard

Required Qualifications:
  • BA/BS or M.S degree in Molecular Biology or Biochemistry or Cell Biology
  • Minimum of 3 years’ experience working in a laboratory research environment in either industry or academia
  • Broad experience and knowledge in common cell biology laboratory procedures (cell culture, ELISA, SDS/PAGE, Western blot, cell transfection, qPCR, immunoprecipitation, fluorescent microscopy, etc.)
  • Experience working with in vivo studies, collection/analysis of tissues, tissue culture is an advantage
  • Experience with use of biological assays to characterize and optimize small molecules and data graphing analysis is an advantage
  • Ability to evaluate and clearly communicate results
     

 
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Wed, 20 Jun 2018 00:00:00 PDT 0
<![CDATA[Scientist - Analytical Chemistry and Formulation]]> Bayside Solutions is seeking a Scientist - Analytical Chemistry and Formulation Development  to be a part of our partner’ s team in the Newark Area. This is an opportunity to work with a startup Biotechnology company focused on providing therapeutics for gastrointestinal diseases.

Our partner’ s culture is fast paced and passionate about innovative drug discovery and development.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Scientist - Analytical Chemistry and Formulation Development 

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.


Summary of Responsibilities:
  • Seeking a versatile Analytical Chemist, preferably with some Formulation Development experience.
  • The primary duties will be in the non-GMP laboratory, analyzing Formulation Development samples and Dose Solutions for numerous non-clinical studies by HPLC with UV detection.
  • Supplemental duties will include media preparation and dissolution testing.

Requirements of Qualification: 
  • A solid understanding of HPLC and analytical chemistry principles is required.
  • Good written and verbal communication skills will be needed for proper notebook write-ups and communication of scientific results to the broader CMC team. 
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Mon, 18 Jun 2018 00:00:00 PDT 0
<![CDATA[Senior Research Associate - Bioanalytical Chemistry]]> Bayside Solutions is seeking a Senior Research Associate - Bioanalytical Chemistry to be a part of our partner’ s team in the Newark Area. This is an opportunity to work with a startup Biotechnology company focused on providing therapeutics for gastrointestinal diseases.

Our partner’ s culture is fast paced and passionate about innovative drug discovery and development.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Senior Research Associate - Bioanalytical Chemistry

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.


Summary of Responsibilities:
  • The candidate will be responsible for sample preparation and execution of existing bioanalytical methods, data analysis and report bioanalytical results for discovery projects, working with two Sr. Scientists in the lab.                         

Requirements of Qualification: 
  • Hands-on experience in LC/MS based bioanalytical methods, quantification of peptides from complex biological matrices and experience with analytical techniques.
  • Experience with the API-4000 instrument and Analyst software is a major plus. 
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Mon, 18 Jun 2018 00:00:00 PDT 0
<![CDATA[Sourcer]]> Bayside Solutions is seeking a talented, results driven Sourcer to be a part of our high-growth organization.  This is a unique opportunity to join a growing team of business professionals focused on building a first in class market-leader in technologies staffing and consulting services.

A successful Sourcer will thrive in a fast-paced environment, have a willingness to do attitude and possess an entrepreneurial spirit.  They also must have an amazing ability to build great relationships both internal peers and business partners as well as externally, with candidates and clients. 

The career of a Sourcer at Bayside Solutions is rewarding, challenging, prosperous and holds ample opportunity for professional growth. Bayside Solutions offers many career path options and a chance to develop an array of skills. Having been recognized as one of the Bay Area’ s fastest growing private companies, we' re ready to provide you with a challenging and rewarding career.

We believe our success  here at Bayside Solutions is a direct reflection of the quality of talented people we hire and develop. New hire training is conducted on a one-on-one basis and covers: recruiting, career consulting and extensive recruiting skills. At Bayside Solutions we make a strong effort and commitment to provide all the tools necessary to ensure the success of every Sourcer.
 

Our Company Bio:

Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at  www.baysidesolutions.com.

 

Job Benefits:
  • An opportunity to join one of the fastest growing private companies in the area, with many possibilities for promotion and career growth
  • Upon receipt of direct hire status, you will be eligible for benefits including medical, dental and vision care, paid time off and holidays totaling more than 20 days a year
  • On the job training with an impressive success rate (more than 50% of our recruiters had no previous industry experience)


Summary of Responsibilities:
  • Entry level - Recruiting Coordinator role.
  • Work in conjunction with our Recruiting Team to develop sourcing strategies to delivery on key critical needs for our clients.
  • Identify resume profiles and conduct in-depth phone interviews to recruit passive candidates in various markets that fit the needs and demands of our clients, both technically and culturally.
  • Seek to understand the candidate’ s business drivers and motivations for exploring new opportunities.
  • Build and maintain on-going relationships with qualified potential candidates in various different markets.

Required Qualifications:
  • Bachelor’ s degree or equivalent experience
  • 1+ years of professional experience with a focus on customer service in a team oriented environment
  • MS Office experience, including Word, Excel, and Outlook
  • Highly self-motivated to not only meet goals and expectations but to exceed them
  • Quick learner, flexible and adaptable to the changing demands of the business
  • Must have the ability to thrive under pressure to meet hard deadlines
  • Must demonstrate the ability to work in a fast-paced, team-centric environment
  • Exceptional ability to multi-task and possess prioritization skills
  • Excellent verbal and written communications

Preferred Qualifications:
  • Ability to build and proactively maintain working relationships with a network of technical professionals
  • Strong organizational and negotiation skills
  • Ability to develop and execute on recruiting strategies
  • Strong interpersonal skills to navigate workflow between the recruiting team, candidates and clients.
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Mon, 18 Jun 2018 00:00:00 PDT 0
<![CDATA[Research Associate I-III]]> Bayside Solutions is seeking a distinctive Research Associate to develop methods for high-throughput microbial strain engineering.

Our client in Emeryville is looking for someone to join a Development team that works in collaboration with partner companies to advance the tools and techniques applied to existing microbes used in large scale industrial fermentation. The Research Associate will work together with other scientists, automation engineers, and software engineers to develop protocols for high-throughput microbial strain engineering, plate models for microbe growth and production, and then enable their use in high throughput workflows.

Our Company Bio:
Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate I-III

Job Benefits
  • An opportunity to significantly impart the future of the company’ s operations.
  • A competitive base salary.
  • On the job training, both in person/online.

Summary of Responsibilities
  • Creating DNA assemblies using cutting edge molecular biology methods.
  • Working with software tools for DNA analysis and design
  • Help with transforming microbes (bacteria, yeast, filamentous fungi).
  • Culturing a variety of host microbes in 96 well format.
  • Use a broad range of analytical methods including PCR, DNA and protein electrophoresis, spectrophotometry, and other plate based assays to qc and test strains.
  • Work with broad range of analytical equipment for high-throughput sample analysis.
  • Preparing materials including media and buffers, managing experiment schedules, processing materials, and collecting, storing and analyzing data.
  • Using automation tools to increase experimental throughput.
  • Actively communicating experimental results to the project team.

Required Qualifications
  •   Bachelor' s Degree, 0-5 years’ experience or Master’ s Degree and 0-3years’ experience.
  •   Molecular biology background, must have significant experience building DNA constructs.  
  • Must have experience troubleshooting cloning projects and feel comfortable doing this independently.
  • Must have experience growing bacteria, yeast or mammalian cell culture.
  • Has experience working with PCR, transformations, and platting cells.  
  • Experience with gram positive staining is a plus.  
  • Some experience with high throughput microbial staining is a plus.  
  • Ideally a resilient team member that is solution seeking and not afraid to try new things.
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Mon, 18 Jun 2018 00:00:00 PDT 0
<![CDATA[Senior Administrative Associate]]> Bayside Solutions is seeking a Senior Administrative Associate  to be part of our client’ s team in the East Bay. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Senior Administrative Associate

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Supports assigned manager and teams with a variety of routine to advanced administrative and operational activities including but not limited to scheduling and coordination of onsite/offsite meetings and/or larger scale events, coordinating domestic and international travel and conference calls, channeling communication and/or materials.
  • Provide support on editing and formatting departmental documents such as memos, reports, presentations and legal documentation that may require data gathering from multiple components.
  • Coordinates the preparation of expense reports, monitors expenses against budget, researches and analyzes discrepancies, creates and submits purchase orders and manual payment requests.
  • Streamlines and reduces unnecessary administrative or operational burdens from manager and other team members.
  • Serves as the department lead on new systems, processes and training compliance. Serves as the departmental “ go-to-person” for general operational or administrative inquiries, requiring broad knowledge of departmental and organizational policies and procedures.
  • Supports the training and onboarding efforts for new staff on administrative processes, systems, practices, tools, etc.
  • Coordinates interview scheduling, office moves, office supply management and department catering.
  • Participates in administrative project initiatives within or outside department/functional area.
  • Provides back-up support to other teams as necessary, demonstrating flexibility, adaptability and positive demeanor in the face of change.
  • Actively participates in internal company meetings with other administrative professionals, finds ways to apply new methods of working, improvements in work processes and supports an exchange of ideas among colleagues.
  • Stays abreast with emerging knowledge and trends in administrative practices and collaborates with colleagues beyond own department.
  •  

Required Qualifications:
  • Associates Degree and above.
  • Advanced computer skills with Microsoft Office applications, Google E-mail, Google Calendar and  Google Drive applications.
  • Experience  with SharePoint is preferred.
  • Advanced organizational and planning skills, including the coordination of multiple activities.
  • Strong attention to detail.
  • Advanced verbal and written communication skills. Communicates clearly, concisely, thoroughly and in a highly professional manner with all internal and external partners/stakeholders.
  • Ability to be flexible and discreet handling sensitive, confidential and complex issues using tact, discretion and mature judgment.
  • Advanced problem solving and decision-making skills.
  • Advanced partnering and negotiation skills and ability to influence others without authority.
  • Strong collaboration skills and ability to partner with other staff to maximize efficiencies across work groups.
  •   Strong interpersonal skills; has a proven track record of developing and maintaining good working relationships with others
  • Require  5 or more years of progressive and directly related administrative support experience to  Director level or above.
  • Experience supporting a manager and department/functional team in the life sciences/biotechnology industry is strongly preferred.
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Fri, 15 Jun 2018 00:00:00 PDT 0
<![CDATA[Scientist I]]> Bayside Solutions is seeking a Scientist I to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Scientist I

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • We seek an outstanding candidate to join Small Molecule Analytical Chemistry and Quality Control in the department to support the Small Molecule Pharmaceutical Sciences team.
  • Responsibilities include the development of chromatographic (HPLC and GC) methods, compound characterization, supporting the development of formulations and manufacturing processes, contribution to problem solving, technical reports, documenting data, and interaction with project teams in a highly cross-functional environment.

Summary of Qualifications:
  • Must have BS, MS, or PhD in a relevant scientific discipline (analytical chemistry or organic chemistry preferred).
  • A minimum of 3 years of professional working experience in analytical chemistry is required.
  • Professional experience in chromatography method development (HPLC and/or GC) is essential.
  • Experience in method development specifically for the analysis of pharmaceuticals is strongly preferred.
  • Candidates must have good theoretical knowledge of analytical and organic chemistry.
  • Mass spectrometry experience is a plus.
  • The position requires excellent organizational and communication skills.
  • Must demonstrated the ability to work independently with sound scientific judgement, and the ability to work as part of a team.
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Thu, 14 Jun 2018 00:00:00 PDT 0
<![CDATA[Clinical Trial Associate]]> Bayside Solutions is seeking a Clinical Trial Associate to be part of our Client’ s team in the South Bay. This is an opportunity to work with a local organization focused on the movement of new drugs or devices from conception to FDA approval.   


The Clinical Trial Associate will be a crucial contributor to the Clinical project teams. Someone with working knowledge of clinical trial documentation, eTMF/TMF, and strong experience with study start-up, maintenance, and close-out would be ideal for this role. Individuals who are passionate about their long-term growth  within an organization and have a proactive mindset would be a great fit for this team.

Our Client’ s culture is founded on core values that keep them committed to being a collaborative, innovative, honest, and adaptable place to work. They have built a family within the workplace, promote employees from within, provide opportunities for professional development, and encourage their employees to be active in their efforts to impact their surrounding communities. This has ultimately created an ideal work environment where you can have a fulfilling and balanced career in clinical research.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

 

Job Benefits:

 
  • An opportunity to join an organization focused on the movement of new drugs or devices from conception to FDA approval.  
  • Work for a company that is local to the beautiful south bay area.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, vacation/PTO, and 401K.

 

Summary of Responsibilities:
  • Set-up, manage, and maintain the Trial Master File (TMF).
  • Obtain, review, process, and track study related documents (CVs, FDA 1572s, lab certifications, IRB approvals, contracts, protocols, etc.).
  • Create meeting agenda/minute templates and provides drafts of meeting minutes.
  • Receive and prepare requests, ship and return Investigational Product supplies.
  • Prepare, ship and manage inventory of study related supplies.
  • Manage and track investigational product supplies for study centers.
  • Gather investigator and site information (addresses, phone numbers, fax numbers, personnel names and email addresses, etc.).
  • Assist in preparing materials for investigator meetings, monitor workshops, and study manuals.

Required Qualifications:
  • RN or B.S. and/or advanced degree in biological sciences or related field or equivalent combination of relevant experience, education or training and previous CTA experience.
  • Strong attention to detail and excellent organizational skills.
  • Advanced proficiency in Microsoft Word and Excel.
  • Willingness to work at the office or at a client' s place of business.

 

Preferred Qualifications:
  • Ability to efficiently perform multiple tasks and manage changing priorities.
  • Ability to identify and solve logistical problems.
  • Ability to read and understand regulatory documents and SOPs.

 

 
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Thu, 14 Jun 2018 00:00:00 PDT 0
<![CDATA[Sr Software Engineer-IC3 (8253693)]]> Senior Software Engineer

Santa Clara, CA

6 months

Principal Duties and Responsibilities include but are not limited to:
  • Plans, designs, develops and tests software systems or applications for software enhancements and new products.
  • Participate in development and testing of Software meeting project deadlines and deliverables.
  • Implementing software solutions that ensure security, integrity, scalability and consistency of critical user data.
  • Solving complex problems in a highly dynamic and agile environment with moderate guidance
  • Working closely with HR, IT Business Analysts and partnering with IT Applications team Supporting
  • Documenting implemented technical solutions and application configuration processes/procedures.

Qualifications: 
  • 5 years of software development experience in enterprise software
  • 5 and/or building web services at scale Minimum 2 year of development
  • 3+ experience in Service Now application customization
  • Deep knowledge of JavaScript, JSON, XML, SOAP, REST and associated frameworks (JQuery, Angular JS)
  • Ability to quickly shift focus and manage/coordinate multiple projects
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Thu, 14 Jun 2018 00:00:00 PDT 0
<![CDATA[Research Associate]]> Bayside Solutions is seeking a friendly, energetic and hardworking Research Associate.  This is a unique opportunity to join a growing team of business professionals focused on treatments to help individuals with diseases that affect the functionality of an individual.

The culture is based on the idea of others. They pride themselves in their commitment to finding cures that other biotech companies have not tackled.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate

This position will support bioanalysis, in vitro ADME studies, formulation, and pharmaceutical characterization for lead/development compounds in support of discovery and development programs.  The ideal candidate will have experience with formulation and/or physicochemical characterization of small molecule drug candidates. He/She will conduct established in vitro ADME assays and bioanalytical analysis as well as assist in the development and validation of in vitro and ex vivo assays to characterize pharmaceutical and ADME properties of small molecule therapeutics.  He/She will participate as a team member and collaborator with a number of diverse departments to contribute to a research effort to validate assays in the areas of drug absorption, metabolism, elimination, clearance and drug-drug interactions.

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Prepare stock solutions/formulations.
  • Prepare biological samples using different extraction techniques.
  • Analyze biological samples and analytical samples by LC-MS/MS and HPLC.
  • Design and execute standard ADME assays.
  • Process and report analytical data.
  • Participate in scientific discussions at Analytical/DMPK group meetings.
  • Present experimental data to the group.

Required Qualifications:
  • A BS/MS in analytical chemistry or related field.
  • 2-5 years of hands-on experience with analytical instrumentation.
  • Knowledge in HPLC and LC/MS operation, instrument maintenance, and troubleshooting is required.
  • Familiarity with a range of laboratory automation instrumentation including robotic liquid handlers - Mechanically inclined.
  • Experience working in DMPK, Analytical, Biology or other related Laboratory
  • HPLC and LC/MS operation experience.
  • A desire to be part of a highly innovative company aimed at transforming the lives of people with serious diseases, their families and society.
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Wed, 13 Jun 2018 00:00:00 PDT 0
<![CDATA[Technical Project Manager]]> Position: Technical Project Manager

Client Industry: Retail

Location: Pleasanton, CA

Terms: Full Time

About Us:  Founded in 2001, Bayside Solutions has been recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: we have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

Our client in East Bay is looking to add a Technical Project Manager to their rapidly growing team. This is a full time opportunity.

About the opportunity: As a Technical Project Manager, you will be responsible for delivering projects within Digital Marketing and e-Commerce business functions. Your tasks include planning, managing, and tracking project activities, scope, risks and budget to ensure successful execution of projects while adhering to the PMO' s methodology and standards. In this role, you will lead application development teams and work in close association with functional IT teams, business stakeholders and company leadership across the globe.

Responsibilities:
  • Provide tactical planning for cross-portfolio programs and systems.
  • Lead and assume accountability for the quality and on-time delivery of the project, with responsibility to provide visibility and necessary reports/updates to senior leadership teams.
  • Foster a healthy work environment that rewards individual and team efforts; encourages creativity while maintaining high caliber productivity and quality.
  • Partner with e-Commerce Product Manager, Enterprise Architecture, IT PMO, Application Development, and Services and Support teams to create detailed plans for both Digital Marketing and e-Commerce initiatives.
  • Follow PMO' s defined methodology and standards, and look for opportunities to improve existing Project Management best practices, including the adoption of industry standard tools, technologies, and methodologies.
  • Track time and attendance of project team members, review vendor invoices and timesheets, review SOWs and Change Orders as necessary for the project needs.
  • Provide thought leadership and help define a vision for the expansion and improvement of a world-class project management organization, addressing elements of culture, recruiting, training, best practices/process, opportunity management, and quality assurance.

Qualifications:
  • At least 5+ years’ experience in project management and software development.
  • Sound knowledge in Project Planning particularly with Microsoft Project software.
  • Experience in an iterative approach for development environments; managing agile/scrum projects is preferred.
  • Must possess superior problem-solving skills, be action-oriented and decisive.
  • Excellent organizational skills and the ability to work under pressure to balance competing priorities in meeting business deadlines.
  • Excellent verbal, written, presentation and interpersonal communications skills.
  • Ability to effectively articulate and present complex concepts, ideas and strategies to senior leadership and end-users.
  • Demonstrated ability to motivate, coach, counsel and train team members.
  • Previous experience with medium to large projects in retail organizations, specifically pertaining to Digital Marketing and e-Commerce business functions will be considered an asset.

Education:
  • Bachelors or Master' s degree in Computer Science or equivalent.

 
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Wed, 13 Jun 2018 00:00:00 PDT 0
<![CDATA[Research Associate, Pharmacology]]> Bayside Solutions is seeking a friendly, energetic and hardworking Research Associate, Pharmacology.  This is a unique opportunity to join a growing team of business professionals focused on treatments to help individuals with diseases that affect the functionality of an individual.

The culture is based on the idea of others. They pride themselves in their commitment to finding cures that other biotech companies have not tackled.

Our Company Bio: 

Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Job Benefits:
  • Offers their employees a great work/life balance.
  • Competitive compensation
  • This position is eligible for medical, vision, dental benefits, paid sick time and 401k.

 

Summary of Responsibilities:
  • Assist in supporting the company’ s pharmacology programs.
  • Conduct and manage in vivo experiments related to the efficacy of novel small molecule compounds
  • Assist the team in identifying, characterizing and advance compounds through research and preclinical development.

Requirements:
  • This position requires a BS/MS in biology, physiology, pharmacology or related field with 0-3 years of relevant research experience
  • Ability to perform basic rodent handling and dosing is required
  • Experience in making physiological buffers
  • Experience in small animal surgery is highly preferred
  • Experience with basic molecular biology techniques (western blot, qPCR) and histology is plus
  • Basic computer skills, including experience with data management and presentation
  • Experience in a pharmaceutical/biotechnology environment is a plus

 
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Tue, 12 Jun 2018 00:00:00 PDT 0
<![CDATA[Global Studies Associate ]]> Bayside Solutions is seeking a Global Studies Associate to be part of our Client’ s team in South San Francisco. This is an opportunity to work with a local Biotechnical company focusing on the discovery, development, manufacturing and commercialization of medicines to treat patients with serious or life-threatening medical conditions.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website atwww.baysidesolutions.com.

Global Studies Associate

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Develops and maintains effective working relationships with members of the SMT involved in running clinical studies.
  • Assists the GSM with effective communication and information sharing within the SMT and with external partners General project support.
  • Provides the SMT with guidance and knows how to support the effective use of system functionality and reports to ensure consistency across SMTs Work in both US & ex-US in-sourced (CCO) & outsourced (CRO) study teams.
  • Will be assigned ≥ 5 clinical trials Works with study vendors & systems expert.
  • Willingness to work on Site Mon – Fri, 8 hr days - remote working opportunity may be considered per department policy.

Required Qualifications:
  • A Bachelor’ s Degree or higher level of education is required.
  • Flexibility to participate in early morning TCs.
  • Candidate displays initiative and resourcefulness to move actions forward without the need for continual supervision.
  • Comfortable working across different cultures & time zones, and with internal, CRO & vendor colleagues.
  • Willingness to complete on-line & instructor-led training: SOP / Healthcare Compliance.
  • Must have the ability to prioritize and multitasks to ensure tasks are completed on time.
  • High level of proficiency in written & oral communication abilities.
  • Ability to perform duties with little oversight from a manager.
  • The successful candidate is self-motivated and can hit the ground running.
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Tue, 12 Jun 2018 00:00:00 PDT 0
<![CDATA[Research Associate IV ]]> Bayside Solutions is seeking a Research Associate IV to be part of our client’ s team in South San Francisco. Imagine yourself collaborating with an organization focusing on the discovery, development, manufacturing, and commercialization of medicines to treat patients with severe or life-threatening medical conditions.

Our Company Bio:  Founded in 2001, Bayside Solutions is one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four-plus years and over 95% repeat business.

Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success!

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate IV

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Candidate will join the Small Molecule Analytical Chemistry and Quality Control in the department of Small Molecule Pharmaceutical Sciences.
  • Responsibilities include the development of chromatographic (HPLC and GC) methods, compound characterization, supporting the development of formulations and manufacturing processes, contribution to problem solving, technical reports, documenting data, and interaction with project teams in a highly cross-functional environment.
  • Ability to work independently with sound scientific judgement, and the ability to work as part of a team.

Required Qualifications:
  • Highly motivated candidate with BS, MS, or PhD degree in a relevant scientific discipline (analytical chemistry or organic chemistry is preferred).
  • Must have a minimum of 2 years of professional working experience in analytical chemistry.
  • Professional experience in chromatography method development (HPLC and/or GC) is essential.
  • Experience in method development specifically for the analysis of pharmaceuticals is strongly preferred.
  • Candidates must have good theoretical knowledge of analytical and organic chemistry.
  • The position requires excellent organizational and communication skills.
  • Mass spectrometry experience is a plus.
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Tue, 12 Jun 2018 00:00:00 PDT 0
<![CDATA[Lab Tech Ops]]> Bayside Solutions is seeking a Lab Tech Ops to be part of our client’ s team in the Branchburg, New Jersey. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Lab Tech Ops:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Perform oligonucleotide purification, characterization, diafiltration and final formulation by following detailed instructions outlined in production batch records and SOPS.
  • Organize work to ensure efficient utilization of time and materials and to complete all procedures in a cGMP compliant manner.
  • Respond quickly and effectively to multiple and changing priorities, rescheduling work effectively to ensure that current and future needs are met. 
  • Accurately and consistently record methods, materials, and results in batch records according to established formats and to keep supervisor informed on status of all projects and of significant findings and results in critical areas.

Summary of Qualifications:
  • Bachelor of Science in Chemistry or related discipline is preferred. 
  • Knowledge in oligonucleotide purification and PCR technology is desirable.
  • Good communication and teamwork skills are required.
  • Ability to work under cGMP guidelines, and coordinate/implement production schedule is necessary. 
  • Strong verbal/written skills are required.
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Thu, 07 Jun 2018 00:00:00 PDT 0
<![CDATA[.NET Developer]]> Our client is seeking a highly talented Senior Application Developer to join their team to help provide internally-developed and third-party software solutions to meet business needs.  This individual will manage technical aspects of assigned projects, including planning and resolving issues.  The Senior Application Developer will also work independently to convert business requirements to Technical Design Specifications, and design/develop code for enterprise-wide and other projects.  This will be a contract-to-hire or direct hire opportunity.

RESPONSIBILITIES
  • Develop software, primarily in C# and ASP .Net
  • Provide expertise in the use of the Microsoft .Net stack, including best practices and design patterns.
  • Significantly contribute to software design and architecture
  • Develop both new applications and improve our existing ones in performance, capability, and reliability
  • Responsible for managing technical development of software from inception through user acceptance, including projects which affect multiple departments and/or pose high risk situations
    • Designs steps and modules, defines timelines, identifies and resolves issues. 
    • May assign work and provide oversight to others
    • May serve as technical lead and make decisions regarding technical direction
  • Presents options and manages client expectations
  • Utilizes design skills to define Technical Design Specifications for complex and high impact projects
  • Creates logic flow charts and process diagrams
  • Creates and/or modifies code to meet specifications
  • Tests and debugs work
  • Supports production software operations during normal business and off-hours
  • Troubleshoots and resolves client issues (May be responsible for client support to an entire business unit)
  • Researches external software solutions

 

QUALIFICATIONS

 

Minimum Requirements:
  • 5-7 yrs. experience in developing software programs; or equivalent combination of education/experience
    • Deep understanding of the C# language and ASP.Net
    • Solid understanding of Enterprise Applications Development and strong design skills
    • Previous experience serving as a team and/or technical lead in software applications development projects preferred
  • Languages/Skills:  C#, ASP.Net, T-SQL, jQuery, JavaScript, HTML5, AJAX, REST, SOA
  • Deep understanding of Web API’ s and micro-service patterns
  • Expert in the Microsoft .Net Runtime through version 4.5, including WCF, LINQ, TPL, and other modern libraries
  • Expert in best practices and design patterns in Microsoft .Net
  • Bachelor’ s degree in MIS, Computer Science, Engineering, Physics, Mathematics, or related discipline
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Thu, 07 Jun 2018 00:00:00 PDT 0
<![CDATA[Facilities Service Coordinator]]> Bayside Solutions is seeking a Facilities Service Coordinator to be part of our client’ s team in the Madison, Wisconsin area. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Facilities Service Coordinator:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Represent the site on project teams that are implementing cross-site platforms, software, polices, or procedures.
  • Support equipment calibration and preventative maintenance activities.
  • Building maintenance and management including.
  • Serve as afterhours contact to support or respond to emergency calls from service providers, city services, the landlord or site leadership; some incidents can be addressed remotely; some will require traveling to the site.
  • Interface with company Real Estate and landlord regarding lease details.
  • Interface with Madison Fire Department when they respond to the site or during inspections.
  • Site planning; physical layout of the site and its update to accommodate needs.
  • Management of materials maintained at an offsite storage warehouse.
  • Management of third-party Facilities contractors and service providers.
  • Support site security and emergency management systems.
  • Critical System monitoring and maintenance; equipment/space monitoring hardware and software.
  • Local response to events (e.g. urgent janitorial services).
  • Local small project execution as requested.
  • Facilities budget development and maintenance.
  • Site Services support; specialty room setup and support of remote lab operations.
  • Facilities correspondence and key metric reporting to company Global Facilities.

Summary of Qualifications:
  • Associates degree in applicable technical field, OR combination of education and experience.
  • 5 years in facilities, construction, or project management role in an FDA regulated facility is preferred.
  • Exceptional organizational and communication skills.
  • Strong cross functional project management skill.
  • Excellent interpersonal skills.
]]>
Thu, 07 Jun 2018 00:00:00 PDT 0
<![CDATA[SQL Developer]]> SR SQL Developer 

Industry: Financial Services

Duration: Contract to Hire (GC or Citizen only)

Location: San Mateo, CA             

Interview Process: Phone, Onsite

Bayside Solutions is seeking an experienced SQL Developer to work on the design, development, implementation and support of client database applications.  The Database Developer will support business functions through use of internally-developed and third-party software solutions, contribute to database and software specifications, and will be responsible for developments and enhancements to computer software programs.  The Database Developer will also perform business analysis, quality assurance testing and database modeling. 

Our Company Bio: Founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

PRIMARY RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO:

It’ s an exciting time to be in our IT department; under the leadership of our newly-appointed Chief Technology Officer, we’ re investing heavily in the future of our firm’ s technology. Our business is growing internationally, which emphasizes the need to build an unparalleled technology team that drives future global growth and scale through strategic solutions and continuous innovation. We play a foundational role in supporting our firm’ s diverse businesses, and we’ re excited to continue solidifying that foundation as we add more talented technologists to our team.

Our IT Department is now seeking a highly talented Database Developer to join our team.  This individual will primarily work on the design, development, implementation and support of Fisher Investments database applications.  The Database Developer will support business functions through use of internally-developed and third-party software solutions, contribute to database and software specifications, and will be responsible for developments and enhancements to computer software programs.  The Database Developer will also perform business analysis, quality assurance testing and database modeling.  This position can be located in our San Mateo, CA, office (near San Francisco, CA) or Camas, WA, office (near Portland, OR).  This will be a contract-to-hire or direct hire opportunity.

RESPONSIBILITIES
  • Database development, reporting development and data migration
    • Perform database design by analyzing business requirements
    • Develop complex SQL queries, stored procedures, and SSIS packages
  • Define and develop a data migration strategy between different products and platforms
  • Optimization and tuning of SQL - Design, develop and migrate SSRS reports
  • Meet with business experts to analyze and document requirements from a database perspective
  • Assist database administrators (DBA) in defining architectural standards for database applications
  • Review applications and database design for compliance
  • Assist in troubleshooting and resolution of database issues
  • Assist in the application development, debugging, configuration and optimization

REQUIREMENTS
  • Must have 7+ years of experience in relational database development or administration in a commercial enterprise setting
  • 7+ year experience in database design, development/administration and implementation experience may be substituted for degree
  • Must demonstrate a clear understanding of the logical and physical database design (for both transactional and data warehouse) and data normalization concepts
  • Must have extensive hands-on experience with MS SQL Server 2012 SSIS, MS SQL Server 2012 SSRS and Transact-SQL

PREFERRED SKILLS/EXPERIENCE:
  • Excellent, proven troubleshooting and problem resolution skills
  • Must have a team-based attitude and be skilled at building constructive and effective relationships
  • Experience with software development life cycle a plus
  • Strong technical documentation skills
  • Financial industry experience is a plus
  • Programming experience with Financial industry experience is a plus

EDUCATION
  • B.S. in Computer Science, Mathematics, or Engineering or equivalent work experience
]]>
Thu, 07 Jun 2018 00:00:00 PDT 0
<![CDATA[Senior Business Analyst]]> IT Business Analyst

Industry: Information Technology, Retail

Location: Rock Hill, SC

Duration: Full Time

 

Join Us

Bayside Solutions is an industry-leading provider of staff augmentation and consulting services. Since 2001, we’ ve built our company around a single concept – relationships. We focus on the people we serve. We’ re straightforward, consistent and 100% accountable. We deliver intelligent solutions that help our clients and candidates thrive.

 

Role

The Business Analyst serves to gather user requirements, create functional requirements documents, develop testing scenarios and scripts, and execute testing to ensure application meets the functional and user interface specifications.  The Business Analyst is also expected to troubleshoot application issues to work with the application provider to resolve.  Serves as a functional and technical resource in Transportation and Freight Payment business areas.

 
  • Provide new capabilities                                                                                                                      
  • Conduct different aspects of systems development life cycle  – ensuring that:
    • Requirements are defined  and documented accurately
    • Test plans are designed and executed successfully
    • Document issues discovered in testing
    • Test resolutions provided by the software vendor.
  • Supporting existing production systems
    • Defining system problems and enhancement requests
    • Ensuring the related fixes and/or enhancements are tested successfully (by IT and by key business partners)
    • Assist with trouble-shooting data issues in relation to processes and other applications.
    • Coach users and executives through change in order to improve data quality and achieve business goals.

 

Required Skills and Qualifications
  • Prior TMS/Freight Payment Implementation experience
  • Small to Mid-size project management experience
  • Familiarity with EDI and XML Integration Mapping
  • Ability to lead other analysts and software provider
  • Demonstrated capability to coach others to improved quality
  • Develop team dynamics
  • Ability to sell the business customer to pursue a path that is good for Ross and IT standards
  • Creative problem-solver
  • Capability to see weeks and months ahead and coordinate people and tasks to accomplish needed goals

 

Preferred Skills
  • Understanding of Transportation industry best practices including Domestic and International, Systemic Bid Processes, Freight Payment
  • Experience with the Microsoft Office Suite including Visio
  • Data manipulation in Excel and/or Access
]]>
Wed, 06 Jun 2018 00:00:00 PDT 0
<![CDATA[Business Systems Analyst]]> Position: Business Analyst

Location: San Ramon, CA

Duration: 6 months

Job Requirements
  • Experienced with  customer on boarding and customer service
  • Managed development of product user guides in a knowledge base
  • Prior knowledge in Cash Management such as Payments (Domestic & International) ACH, Wires, Transfers, RTP, Bill Pay, Payments Services: Positive Pay, Reverse Pay, Stop Pay, Collaboration
  • Alerts/Messaging/Chats: Security and Fraud prevention
  • Strong experience with Information reporting/Reports: Online, Mobile and Host to Host Channels, Mobile App, API Banking


  • Position: Business Analyst
    Location: San Ramon, CA
    Duration: 6 months
    Job Requirements:
  • Experienced with customer on boarding and customer service
  • Managed development of product user guides in a knowledge base
  • Prior knowledge in Cash Management such as Payments (Domestic & International) ACH, Wires, Transfers, RTP, Bill Pay, Payments Services: Positive Pay, Reverse Pay, Stop Pay, Collaboration
  • Alerts/Messaging/Chats: Security and Fraud prevention
  • Strong experience with Information reporting/Reports: Online, Mobile and Host to Host Channels, Mobile App, API Banking
  • Experience with Waterfall, BRD, UAT, QA Coordiantion, Data Analyst(great plus)

  • Nice to have: Appian or MS Dynamics experience
]]>
Tue, 05 Jun 2018 00:00:00 PDT 0
<![CDATA[Project Manager 5]]> ROLE:                  Senior Program Manager

LOCATIONS:       San Ramon CA

INDUSTRY:          Banking

 

Bayside Solutions is seeking a Program Manager to Lead, organize, and coordinate programs (collection of related projects/work streams) that provide strategic value to the organization. A successful candidate will provide guidance to teams and project managers to promote the company’ s culture and commitment to excellence in delivery execution. The ideal candidate will be an excellent leader and will have experience in managing staff of different disciplines to produce results aligned to expectations; they will also be able to develop efficient strategies and tactics the successfully delivery the program on time, on budget, on scope. The goal is to ensure that all projects and the program deliver exceptional value to our client’ s organization.

 

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

 

PRIMARY RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO:
  • Formulating, organizing and monitoring inter-connected projects (interdependencies)
  • Coordinate executive management and provide suitable strategies and objectives for program delivery
  • Manage cross-project activities, including; statusing, issue/risk escalation, roadblock removal, and transparency into the body of work
  • Lead, evaluate, and coach project managers and other staff
  • Develop and control deadlines, budgets and activities
  • Apply change, risk and resource management best practices
  • Analyze program risks and recommend appropriate actions to mitigate
  • Assume responsibility for the program’ s people and vendors
  • Assess program performance and aim to maximize ROI and value delivery
  • Resolve projects’ higher scope issues
  • Effective change management for the interconnected-projects
  • Develop and manage stakeholder communications and ensure transparency regarding issues and decisions
  • Ensure project and program goals are achieved.

 

REQUIREMENTS
  • Ability to evaluate larger picture for program and provide approach for the most effective path to completion
  • Proven experience as a Program Manager (Managed multiple projects/work streams under one program umbrella)
  • Thorough understanding of project/program management techniques and methods
  • Excellent Knowledge of performance evaluation and change management principles
  • Outstanding leadership and organizational skills
  • Excellent communication skills
  • Excellent problem-solving ability Exceptional relationship management skills and ability to be an “ influencer”
  • Excellent knowledge of MS Office; working knowledge of program/project management software (CA PPM, Basecamp, MS Project etc.) is a strong advantage

 

EDUCATION
  • Bachelor’ s Degree in a STEM related field required
  • Master’ s Degree in a STEM related field preferred

 
]]>
Tue, 05 Jun 2018 00:00:00 PDT 0
<![CDATA[Global Studies Manager]]> Bayside Solutions is seeking a Global Studies Manager to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Global Studies Manager

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Provides direction and leadership to one or more clinical operations teams.
  • Develops operational plans including site monitoring strategies, risk mitigation strategies, trial budgets, site selection, and clinical supplies management.
  • Builds effective and efficient high performing operations teams and ensures team members are aware of their accountabilities, responsibilities and deliverables.
  • Contributes to the development and management of the study timelines, resources, budget, risk and quality plans.
  • Provides clinical operations expertise to ensure operational feasibility and delivery.
  • Oversees forecasting of clinical/non-clinical supplies.
  • Delivers the operational elements of the study plan.
  • Provides the day-to-day operational management of CROs and vendors to ensure delivery against contracted scope of work.
  • Identifies areas of best practice and process improvements.
  • Ensures study adherence to ICH/GCP and SOPs.

Summary of Qualifications:
  • Life sciences degree or nursing equivalent and 5-7 years of experience as a Global Studies Manager in a clinical research/a healthcare environment.
  • Proven clinical development experience of the operational aspects of all stages of clinical studies preferably working in a Global environment and/or including monitoring or leading affiliate teams, working with vendors and/or CROs, drug supply management and planning operational activities to achieve database lock.
  • Experience of project managing operational aspects of a clinical study including development of timelines, budgets and resource plans.
  • Good knowledge of ICH GCP.
  • Proven ability to successfully achieve results within a multi-cultural and geographically diverse team.
  • Experience of working as a part of a large team and leading small study or functional teams, with a proven ability to be an active member of the team and motivate and lead a small team to deliver against commitments.
  • Well-developed written and verbal communication skills demonstrated by an ability to present clear instruction/direction to teams at the same level in the organization and influence at higher levels in the organization.

 
]]>
Tue, 05 Jun 2018 00:00:00 PDT 0
<![CDATA[Senior IT Project Manager]]> IT Project Manager

Tempe, AZ

6 months plus Contract


Primary Responsibilities Include But Are Not Limited To:
  • Develop, track and manage project budget, project plans, timelines and scope.
  • Manage project resources including procuring project staff, developing, motivating, coaching and advising.
  • Partner closely with other members of functional project teams to define business requirements.
  • Lead teams of developers in the delivery of high-quality software solutions that meet business needs.
  • Define test plans and ensure that products are defect free before User Acceptance Testing.
  • Facilitate the User Acceptance Testing process, developing rollout plans and procedures.
  • Prepare and present cost-benefit analyses.
  • Ensure appropriate systems development and project management processes are being utilized.
  • Make presentations to steering committees or project sponsors.
  •  

Qualifications
  • Bachelor' s degree in a STEM related field required. MBA or other related advanced degree preferred.
  • Project Management Certification
  • 7+ years’ of experience managing projects in a Banking or Financial Services environment
  • Demonstrated ability to be flexible/ adaptable in exercising judgment in a changing environment and to manage competing priorities.
  • Proven ability to learn business processes quickly and to work well with business partners at different levels within the organization.
  • Strong ability to assess risk and apply management principles to technology applications/products and business functions.
  • Experience delivering technology and business application solutions in a large-scale, multi-platform systems environment.
]]>
Tue, 05 Jun 2018 00:00:00 PDT 0
<![CDATA[Research Associate, Histology]]> Bayside Solutions is seeking a Research Associate, Histology to be part of our client’ s team in Redwood City. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate, Histology:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Responsible for tissue processing (FFPE and fresh frozen) and slide preparation.
  • Proper maintenance/tracking of collected samples and slides.
  • Conduct immunohistochemical and immunofluorescent staining on mammalian tissue sections.
  • Produce experimental results using microscopy.
  • Coordinate activities with project team members.
  • Collaborate with project team members to discuss experiments and data.
  • General lab duties such as preparation of reagents and stocking of supplies.
  • Follow laboratory safety guidelines and practices.

Summary of Qualifications:
  • Bachelors of Science or Masters in biology or related discipline with at least 2 years of lab experience.
  • Experience in tissue processing, histological slide preparation, and immunohistochemical and immunofluorescent staining in mammalian tissues required.
  • Must have excellent organization and planning skills and the ability to work under timeline in a fast-paced environment.
  • Excellent written and oral communication skills.
]]>
Mon, 04 Jun 2018 00:00:00 PDT 0
<![CDATA[Engineer I]]> Bayside Solutions is seeking an Engineer I to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Engineer I:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Support new product design, development and implementation of delivery devices and novel injection tools/aids for biologic therapeutics. 
  • Primary technologies include auto-injectors, basal infusers/pumps, and needle stick prevention devices utilizing pre-filled syringes and cartridges.   
  • Execution of mechanical and analytical testing to support the selection, design verification, commercialization and marketing of various designs. 
  • This will include the execution of routine and on-going R&D stability testing, design verification testing, complaint investigations and special testing requests. 
  • Work with design engineers to identify, develop, implement, qualify and validate new testing methods (and equipment if required) to meet capability and capacity needs of the project, troubleshoot equipment failures, and ensure sample traceability and data integrity. 
  • The person will provide input and execute plans to maintain and improve laboratory safety. 
  • Support the design engineer in data analysis and interpretation, to identify questionable results and identify root cause.

Summary of Qualifications:
  • B.S. or M.S. in engineering, physical, chemical, or biological sciences.
  • 2-3 years experience in the Pharmaceutical, Biotech or Medical Device industry is preferred.
  • Direct experience in executing physical test methods, equipment procurement, and qualification of equipment.
  • Familiarity with statistical tools such as JMP or Minitab, and execution of Gage R&R or similar measurement systems analyses.
  • Experience with statistical handling and interpretation of data, technical report writing and reviewing.
  • Expertise in electrical/mechanical instrumentation, data acquisition, and equipment maintenance.
  • Prior experience working in a matrix organization with a highly cross-functional and collaborative environment.
]]>
Mon, 04 Jun 2018 00:00:00 PDT 0
<![CDATA[MS Dynamics GP Developer/Analyst]]> MS Dynamics Great Plain (GP) Developer / Analyst         

Industry: Financial Service

Duration: Full Time/Direct Hire

Location: San Mateo, CA             

Interview Process: Phone, Onsite

 

Join Us

Bayside Solutions is an industry-leading provider of staff augmentation and consulting services. Since 2001, we’ ve built our company around a single concept – relationships. We focus on the people we serve. We’ re straightforward, consistent and 100% accountable. We deliver intelligent solutions that help our clients and candidates thrive.

 

We Have
  • Support all aspects of software or hardware related to MS Dynamics GP including routine maintenance, databases, installs, updates, patches, customizations, integrations, etc. including 3rd party applications
  • Set up/maintain GP configurations on the servers and terminals
  • Ability to write, troubleshoot and analyze SQL procedures to extract/view/edit database
  • Communicate effectively with internal and external resources necessary to successfully complete assignments or projects
  • Administer GP end users, roles, security and all 3rd party associated
  • Troubleshoot and resolve daily support tickets and help requests
  • Upkeep on documentations, work instructions, procedures on SharePoint
  • Proactively managing and prioritizing multiple GP related projects, assignments, timelines, milestones and follow-up communications
  • Conduct end-user training for MS Dynamics GP
  • Help in creating best practices and suggestions to improve processes, business solutions, maintain data integrity and security
  • Assist in any other duties within IT Department

 

You Have
  • 5+ years C#/.NET/SQL Server developer with experience in Windows and Web Application development.
  • Hands on experience with MS Dynamics GP Development and Customization  (2010/2015 or newer)
  • Experience with Integrations (smartconnect, integration manager)
  • Experience doing Dynamics GP Implementations/Upgrades
  • Proficiency in Dynamics GP Core Financial Modules
  • Experience with MS SQL, SSRS, PowerShell scripting

 

Competitive Advantage
  • Microsoft Great Plains Certification
  • Prior experience implementing MS GP Dynamics in an enterprise environment

 

 

 
]]>
Mon, 04 Jun 2018 00:00:00 PDT 0
<![CDATA[Engineer III]]> Bayside Solutions is seeking an Engineer III to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Engineer III:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • The engineer is responsible for design, development, and implementation of drug delivery devices for parenteral pharmaceutical therapeutics.
  • Primary technologies include vial transfer systems, manual injection systems, automated injection systems, and interfaces with pre-filled syringes.
  • The engineer is a technical expert and provides technical leadership in the development and commercialization of new drug-device combination products in collaboration with company’ s engineering, scientific, and manufacturing organizations.
  • The engineer will work with his/her team to ensure that device design, component selection, manufacturability and test methods meet product needs. 
  • Responsibilities include drafting Design Control documents including reports, protocols, plans & specifications, conducting and participating in/leading root cause analyses, participating in cross-functional teams, managing design verification testing and evaluation of device design, assembly & test equipment.
  • Drive problem-solving activities using state of the art tool such as DMAIC, DFFS, DOE, Monte Carlo Simulation, Probabilistic Design. 
  • The engineer regularly interfaces with staff and leaders in Device Development and may interface with Commercial Marketing, Clinical Sciences, Contract Manufacturing, Product Core Teams, Pharmaceutical Development, Packaging Development, Quality and Regulatory Affairs. 
  • The engineer may also interact with external development partners and component suppliers.  

Summary of Qualifications:
  • Advanced degree (M.S.) in engineering required. Mechanical, Biomedical, Chemical Engineering preferred.  
  • 4-6 years of relevant experience preferred.
  • Experience in full cycle (concept – commercialization) of medical device development, system engineering, injection molding and mold-flow analyses, mechanical modeling methods, medical device risk management, medical device design control requirements, test method development and validation.
  • Experience in the Pharmaceutical, Biotech or Medical Device industry is a must, with previous work on development of injection devices required. 
  • Prior experience working on primary containers, needle safety systems, injection devices with automated features, and  container-device  compatibility and interactions is highly desired.
  • A proven track record of working effectively in a matrix organization with a highly cross-functional and collaborative environment is very desirable.
  • Excellent communication skills are required.
]]>
Mon, 04 Jun 2018 00:00:00 PDT 0
<![CDATA[Process Manager]]> Bayside Solutions is seeking a Process Manager to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Process Manager:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Work closely with the business to identify and analyze core business processes and workflows to improve the processes and identify opportunities and potential solutions on a variety of process and quality improvement projects and activities.
  • Responsible for analyzing, refining and developing processes through implementation and will contribute to the ongoing programmatic effort to build or refine effective global and cross-functional controlled documents (including policies, procedures, templates and forms) in a manner conducive to the business.
  • Serve as a change agent for; disseminating information, driving standardization and collaboration, resolving issues, and assisting teams with effectively implementing process improvements internally and externally as project impacts dictate.
  • Organize and facilitate teams to critically review current processes for effectiveness, quality and simplification and identify implementation requirements requiring cooperation and support from cross functional stakeholders/business partners; establishing links between business strategy needs and process improvement initiatives.
  • Elicit requirements using interviews, document analysis, requirements workshops, surveys, site visits, business process descriptions, use cases, scenarios, business analysis, tasks and workflow analysis.
  • Develop procedural documents, including process maps, working documents and clinical study manuals in compliance with regulatory requirements and global processes.
  • Collaborate with PTM, gRED subject matter experts and business partners to ensure appropriate documentation and controlled document requirements are identified and integrated in process maps (business requirements).
  • Routinely prepare reports by collecting, analyzing, and summarizing information as required.
  • Regularly attend PTM and cross functional staff meetings to present project and process improvement activity status.
  • Serve as internal advisor to address process related questions from personnel and gather information to distinguish requests from true business needs.
  • Develop tools, templates and procedural documents to support the tactical application of business processes as required.
  • Routinely solicit feedback from users on process enhancements, training and other means of driving more effective utilization and systems and process integration.
  • Provide input to training programs and team effort by accomplishing related results as needed.

Summary of Qualifications:
  • Bachelor’ s degree and a minimum of 8 years of experience working in pharmaceutical or healthcare related industry or 6-9 years with Master (E4 level).
  • Minimum 3-5 years of experience as a Process/Business Analyst or equivalent.
  • Knowledge of the drug development process, GCP/ICH requirements highly desired.
  • Advanced understanding of the Microsoft Office Suite; proficient in use of MS Word, Excel and Power Point.
  • Must have demonstrable ability to learn new systems and develop procedures to support new systems.
  • Past experience working with FDA or a regulated environment.
  • Understanding of GCP, ICH and core document management practices.
  • BPM and/or Six Sigma certification.
  • PMP or quality processes certification Competencies Identified for Success.
  • Strong skills in process mapping and business process re-engineering.
  • Strong analytical skills with a demonstrated ability to extensively analyze business processes and workflows.
  • Experience facilitating workshops and focus groups.
  • Experience developing business requirements.
  • Experience developing procedural documentation and presentations.
  • High level of competence with MS Office and MS Visio.
  • Ability to: influence with or without authority, facilitate groups with diverse perspectives, and bring teams to consensus/alignment.
  • Adept in critical thinking with demonstrated analytical, problem solving skills.
  • Excellent planning and prioritization skills with ability to multitask and adapt in a fast-paced environment.
  • Able to synthesize large amounts of information.
  • Able to deliver results despite shifting environment.
  • Excellent verbal and written communication skills and the ability to interact professionally with a diverse group, executives, managers, and subject matter experts.
  • Detail oriented with the ability to work independently and prioritize multiple tasks efficiently.
  • Strong project management skills.
]]>
Thu, 31 May 2018 00:00:00 PDT 0
<![CDATA[Study Data Manager I]]> Bayside Solutions is seeking a Study Data Manager I to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Study Data Manager I:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Acts as a core member of Study Management Teams and serves as the study data management contact at the study and/or program level, providing expert guidance to program teams.
  • Leads the CDM study team and maintains oversight of all study start-up, study conduct and study close-out data management issues, activities and deliverables for one or more studies. Interacts regularly with Clinical Data Management groups to ensure that project objectives are understood and met.
  • Performs the following: provides early strategic input into protocol design focused on data management issues:
    • Leads the development of eCRFs and database development and testing specifications by interacting with other functional area representatives.
    • Responsible for the oversight of all data review and cleaning activities involving close interaction with project clinical research professionals.
    • Responsible for the implementation of standards within Study Data Management across one or more CDM study teams; develops and executes ad hoc database queries utilizing data review and query tools.
    • Manages projects resourced externally via contract research organizations or corporate partners.

Summary of Qualifications:
  • B.A./B.S. or equivalent with a minimum of 5 years of experience in Clinical Data Management.
  • Knowledge of core clinical data management applications (Clinical data management systems, electronic data capture, query tools, web browser, MS Office suite).
  • Clinical data management system experience (EDC Medidata Rave preferred).
  • Ability to apply advanced principles, theories and concepts for CDM as a whole.
  • Understanding of the conceptual basis for data management conventions, standards and processes.
  • Good understanding of the role of data management, biostatistics and statistical programming in the drug development process.
  • Ability to develop solutions to complex problems.
  • Ability to multi-task and effectively set own priorities.
  • Strong organizational skills.
  • Strong communication and interpersonal skills.
]]>
Wed, 30 May 2018 00:00:00 PDT 0
<![CDATA[Senior Scientist]]> Bayside Solutions is seeking a Senior Scientist  to be a part of our partner’ s team in the Newark  area. This is an opportunity to work within a life-changing biotechnology company poised to change the neuro-modulator aesthetic and therapeutic product categories.

Our Company Bio:  Bayside Solutions was founded in 2001, and recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Senior Scientist 

Job Benefits:
  • An opportunity to join a bio-technology company developing and delivering next-generation neuromodulator, daxibotulinumtoxinA, and highly purified botulinum toxin  type  A.
  • Work for a company that likes to dream and think big! They are local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Supporting the development of new bioassay, by assisting lead scientist with preparation of buffers, and other routine work
  • Generate supporting document, SOP’ s, reports, etc. to support assay development
  • Detail-oriented and excellent organization abilities
  • Self-motivated, fast-learner and able to follow instructions
  • Enjoys working independently under general direction in a fast-paced, multi-tasking environment

Summary of Qualifications:
  • 5+ years of industry experience. 
  • Able to apply analytical skills and judgment in assessing the quality of data and instrument/method performance. 
  • Experience with CE SDS is a must. 
  • Experience with method development is a must.  
  • Hands on experience with ELISA or Western Blot nice to have. 
  • Hands on experience in chromatography (HPLC) is a plus.
  • Experience in instrument and method troubleshooting is highly desirable.
  • Experience in the analysis of pharmaceuticals is a plus.
  • Must be self-motivated, able to multi-task, and meet timelines efficiently and productively
  • Prepare solvents for various team members
  • Adhering to all laboratory SOPs relating to personal safety & chemical hygiene
  • Bachelor of Science degree in a related biotech discipline preferred.
  • Quick leaner
  • Excellent organization and communication skills.
  • Attention to detail is a must.
  • Ability to learn new skills related to all aspects of work.
  • Perform work in a neat and timely manner.
  • Ability to work as part of a team.
]]>
Tue, 29 May 2018 00:00:00 PDT 0
<![CDATA[Sr. Scientist (Formulation)]]> Bayside Solutions is seeking an Sr. Scientist (Formulation)  to be a part of our partner’ s team in the Newark  area. This is an opportunity to work within a life-changing biotechnology company poised to change the neuromodulator aesthetic and therapeutic product categories.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Associate Scientist/Scientist, Formulation

Job Benefits:
  • An opportunity to join a bio-technology company developing and delivering next-generation neuromodulator, daxibotulinumtoxinA, and highly purified botulinum toxin  type  A.
  • Work for a company that likes to dream and think big! They are local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Strong organizational and communication skills.
  • Designs and/or conducts pre-formulation, formulation development, process development, process optimization, scale-up and clinical manufacturing on assigned projects
  • Hands on knowledge of Design of experiments (DOE), knowledge of Six Sigma is a plus
  • Serves as a subject matter expert in formulation, process and product development, optimization and scale-up of parenteral formulations.
  • Maintains accurate, detailed records of work performed following good documentation practices.
  • Writes and reviews protocols, batch records, batch summary reports, technical transfer documents and product development reports and other key reports/documents as per ICH guidelines and regulatory requirements.
  • Train and supervise more junior team members.

Required Qualifications:
  • Experience in various modern analytical assays, applicable to protein therapeutics.
  • Hands-on experience in using methods for protein analysis, including but not limited to UV, HPLC/UPLC, IEF, and CE-SDS
  • Familiarity with biophysical methods for protein characterization, such as CD, DSC, MFI, and light scattering, is a plus
  • Excellent interpersonal and communication skills in a team-oriented environment are required. 
  • Ability to work independently as well as within a team, handle multiple projects, demonstrate initiative and accountability, and strong attention to detail. 
  • Experience in variety of formulations with emphasis on parenteral.
  • Able to collaborate with individuals in a one-on-one setting and cross-functional teams and mentor/lead individuals within the Formulation Development group.
  • Expertise in pharmaceutical development, novel drug delivery systems, process and product development experience. Should have knowledge of Current Good Manufacturing Practices and Standard Operating Procedures as related to laboratory/manufacturing environment.
  • Excellent verbal and written communications skills are essential.
  • Should have basic understanding of the Food Drug Administration guidelines and regulations.
  • Working knowledge of Microsoft suite of software products including Excel, Word, and PowerPoint.
  • Education:
    • PhD in Pharmaceutics and/or  related scientific field; preferably in Formulation Development/Drug Delivery and a minimum of 2 years of relevant experience  
    • Master' s degree in Pharmaceutical Sciences with emphasis in Pharmaceutical Formulation and Technology and a minimum of 8 years of relevant experience.
]]>
Tue, 29 May 2018 00:00:00 PDT 0
<![CDATA[Research Technician I]]>
Bayside Solutions is seeking a Research Technician I to be part of our client’ s team in the South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Technician I

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Support and/or lead cell culture experiments.
  • This is a lab-intensive role in which primary activities include cleaning, prepping, sampling, batching, monitoring and harvesting bioreactors along with data analysis.
  • Author and/or review internal technical documents.
  • Contribute to cell culture technology development projects.
  • May interact with Quality, Regulatory, and Manufacturing organizations.
  • May act as a representative in multidisciplinary project teams and present data when necessary.
  • Act as a resource within the department in a recognized area of technical expertise.

Summary of Qualifications:
  • BS or MS in Biology, Chemistry, Chemical Engineering or similar with a minimum of 1-2 years bio/pharmaceutical process development experience.
  • Knowledge of Current Good Manufacturing Procedures compliance a plus.
  • The position requires strong leadership, collaboration, communications, prioritization, and problem solving skills.

 
]]>
Fri, 25 May 2018 00:00:00 PDT 0
<![CDATA[Sr. Employee Relations Manager]]> Bayside Solutions is seeking a Sr. Employee Relations Manager to be part of our client’ s team in the South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at  www.baysidesolutions.com.

Sr. Employee Relations Manager

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Act as the single point of contact for all employee relations matters within assigned client groups.
  • Act as the primary investigator of employee complaints, including, but not limited to those involving allegations of discrimination, sexual harassment and/or hostile work environment.
  • In consultation with the Legal Department, work with clients to ensure compliance with company policies and applicable employment laws and serve as a company resource for effective risk mitigation strategies.
  • Identify opportunities to instill sound ER practices that are in alignment with company goals and objectives.
  • Effective, timely and consistent utilization of the Employee Relations case management system.
  • Will have the capacity for leveraging the involvement of key stakeholders of all levels in the resolution of ER initiatives and solutions.
  • Will have the ability to effectively collaborate with other members of the HR team, internal and external Legal.

Summary of Qualifications:
  • Bachelor’ s Degree or equivalent work experience.
  • 10 to 15 years of progressively responsible HR and/or business experience, which includes at least 7 years’ experience working on highly complex employee relations issues.
  • Proven track record in consistently meeting or exceeding identified annual work goals, including significant contribution to strategic goals and/or policies, programs, practices of the organization.
  • Deep and broad expert level technical knowledge and expertise in Employee Relations.
  • Demonstrated ability to apply expert knowledge of state and federal employment laws and regulations, as well as the ability to diagnose and develop appropriate solutions to complex cross-organization and/or cross-Company issues.
  • Requires a high-level collaboration and teamwork.
  • Must have a proven ability for decision making.
  • Demonstrated consultation and influencing skills at all levels.
]]>
Wed, 23 May 2018 00:00:00 PDT 0
<![CDATA[Manufacturing Bioprocess Technician]]> Bayside Solutions is seeking a Manufacturing Bioprocess Technician  to be part of our client’ s team in Vacaville. This is an opportunity to work with one of the largest Biopharmaceutical companies in the world developing innovative medicine to improve the quality of patients’ lives.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Manufacturing Bioprocess Technician

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Support the Manufacturing department by working effectively to meet department goals, objectives and tasks to achieve desired results.
  • Responsible for completing assigned tasks which include cleaning, sterilizing, and prepping parts used in the manufacturing environment.
  • Provides timely and accurate verbal and written communications of processing updates, discrepant events, and scheduling delays.
  • Work with senior technicians and leads to prioritize tasks and assignments and make recommendations to maximize efficiency and productivity based on shift needs.
  • May also include stocking, inventory and environmental monitoring.

 

Summary of Qualifications:
  • Bachelor' s Degree in Life Sciences or Engineering.
  • Equivalent education with a minimum of 2 years of work experience will be considered as well.
  • Must possess solid problem solving, interpersonal communication, and team-based skills.
  • Demonstrated experience and knowledge of working in a GMP environment compliantly and safely.
  • General skills: working with pressurized systems / high temperatures / acidic & basic solutions, follow Standard Operating Procedures (SOPs), making manual connections.
  • Specific skills: chromatography/TFF/UFDF processing, preparing buffer/media solutions, chromatography column packing, SAP, Trackwise.
  • Must be a self-starter with strong focus on quality, details, results and application of cGMP.
  • Must be able to work weekends and off shifts.
]]>
Tue, 22 May 2018 00:00:00 PDT 0
<![CDATA[Research Associate III]]> Bayside Solutions is seeking a Research Associate III to be part of our client’ s team in the South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate III:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Work alongside a group of researchers evaluating novel therapies in the field of cancer immunotherapy.
  • Explore mechanism of action, combinatorial therapeutic strategies, and elucidate biomarkers to support the identification of companion diagnostics that are predictive of therapeutic response.
  • Work closely with discovery scientists to advance research stage programs into early clinical development, providing both scientific and technical expertise. 

Summary of Qualifications:
  • MS degree in immunology, oncology, biology or related field, PhD strongly preferred.
  • Minimum of 8 years of hands-on relevant experience with a track record of success as evidenced by a strong publication record, and/or, evidence of sustained contributions in the biopharmaceutical industry required.
  • Must have demonstrated expertise of a wide range of cellular and biochemical assays, including cell isolation and culture, molecular biology, flow cytometry, cellular immunology assays and familiarity with in vivo models of immune disease or oncology are required.
  • Excellent communication skills, can present research at intra- and inter-departmental meetings, and work effectively as part of a team is a must.
  • Experience in Cytof and/or high dimensional flow cyotmetric analysis is highly desirable.
  • Qualified candidates should be adept at independently designing, executing and interpreting experiments.
]]>
Tue, 22 May 2018 00:00:00 PDT 0
<![CDATA[Sourcer]]> Bayside Solutions is seeking a talented, results driven Sourcer to be a part of our high-growth organization.  This is a unique opportunity to join a growing team of business professionals focused on building a first in class market-leader in technologies staffing and consulting services.

A successful Sourcer will thrive in a fast-paced environment, have a willingness to do attitude and possess an entrepreneurial spirit.  They also must have an amazing ability to build great relationships both internal peers and business partners as well as externally, with candidates and clients. 

The career of a Sourcer at Bayside Solutions is rewarding, challenging, prosperous and holds ample opportunity for professional growth. Bayside Solutions offers many career path options and a chance to develop an array of skills. Having been recognized as one of the Bay Area’ s fastest growing private companies, we' re ready to provide you with a challenging and rewarding career.

We believe our success  here at Bayside Solutions is a direct reflection of the quality of talented people we hire and develop. New hire training is conducted on a one-on-one basis and covers: recruiting, career consulting and extensive recruiting skills. At Bayside Solutions we make a strong effort and commitment to provide all the tools necessary to ensure the success of every Sourcer.
 

Our Company Bio:

Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at  www.baysidesolutions.com.

 

Job Benefits:
  • An opportunity to join one of the fastest growing private companies in the area, with many possibilities for promotion and career growth
  • Upon receipt of direct hire status, you will be eligible for benefits including medical, dental and vision care, paid time off and holidays totaling more than 20 days a year
  • On the job training with an impressive success rate (more than 50% of our recruiters had no previous industry experience)


Summary of Responsibilities:
  • Entry level - Recruiting Coordinator role.
  • Work in conjunction with our Recruiting Team to develop sourcing strategies to delivery on key critical needs for our clients.
  • Identify resume profiles and conduct in-depth phone interviews to recruit passive candidates in various markets that fit the needs and demands of our clients, both technically and culturally.
  • Seek to understand the candidate’ s business drivers and motivations for exploring new opportunities.
  • Build and maintain on-going relationships with qualified potential candidates in various different markets.

Required Qualifications:
  • Bachelor’ s degree or equivalent experience
  • 1+ years of professional experience with a focus on customer service in a team oriented environment
  • MS Office experience, including Word, Excel, and Outlook
  • Highly self-motivated to not only meet goals and expectations but to exceed them
  • Quick learner, flexible and adaptable to the changing demands of the business
  • Must have the ability to thrive under pressure to meet hard deadlines
  • Must demonstrate the ability to work in a fast-paced, team-centric environment
  • Exceptional ability to multi-task and possess prioritization skills
  • Excellent verbal and written communications

Preferred Qualifications:
  • Ability to build and proactively maintain working relationships with a network of technical professionals
  • Strong organizational and negotiation skills
  • Ability to develop and execute on recruiting strategies
  • Strong interpersonal skills to navigate workflow between the recruiting team, candidates and clients.
]]>
Mon, 21 May 2018 00:00:00 PDT 0
<![CDATA[Account Executive]]> Bayside Solutions is seeking a talented, results driven Account Executive to be a part of our high-growth organization.  This is a unique opportunity to join a growing team of business professionals focused on building a first in class market-leader in technologies staffing and consulting services.

A successful Account Executive will thrive in a fast-paced environment, have a willingness to do attitude and possess an entrepreneurial spirit.  They also must have an amazing ability to build great relationships both internal peers and business partners as well as externally, with candidates and clients. 

The career of an Account Executive at Bayside Solutions is rewarding, challenging, prosperous and holds ample opportunity for professional growth. Bayside Solutions offers many career path options and a chance to develop an array of skills. Having been recognized as one of the Bay Area’ s fastest growing private companies, we' re ready to provide you with a challenging and rewarding career.

We believe our success here at Bayside Solutions is a direct reflection of the quality of talented people we hire and develop. New hire training is conducted on a one-on-one basis and covers: recruiting, career consulting and extensive recruiting skills. At Bayside Solutions we make a strong effort and commitment to provide all the tools necessary to ensure the success of every Account Executive.

 

Our Company Bio:

Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at  www.baysidesolutions.com.

 

Job Benefits:
  • An opportunity to join one of the fastest growing private companies in the area, with many possibilities for promotion and career growth
  • Upon receipt of direct hire status, you will be eligible for benefits including medical, dental and vision care, paid time off and holidays totaling more than 20 days a year
  • A competitive base salary and commission structure based on revenue generated
  • Car allowance
  • Cell phone allowance
  • Mileage reimbursement

Summary of Responsibilities:

This is a business development role that requires a successful business professional to develop and execute on a strategy to generate sales revenue by building a maintaining client relationships, seeking to understand the client’ s business needs and initiatives and selling Bayside Solutions’ wide breadth of service offerings to craft a solution to address the client’ s business needs and demands.  The role’ s responsibilities include, but are not limited to:
  • Engage in new and existing client business development activities.  Activities include, but are not limited to: cold calling, qualifying initial clients, identifying potential decision makers, establishing contact relationships, completing company/department profiles and organizational charts, marketing candidates, scheduling and conducting new and follow-up client visits.
  • Develop and execute on business development strategy for market penetration
  • Ability to engage prospective clients confidently; determine interests and motivators of key decision-makers.
  • Qualify opportunities, create target lists for vertical markets
  • Develop superior customer relationships through client meetings, lunches and other out of office activities.
  • Consistently achieves sales quota
  • Conduct market research and qualify target accounts within the local geography. Keep current on market dynamics and trends within specific markets and regions and forecast client demands.
  • Establish client expectations and effectively communicate to appropriate parties to ensure customer satisfaction
  • Facilitate development of professional service agreements (including negotiation of terms when necessary) between Bayside Solutions and clients.
  • Ability to engage prospective clients confidently; determine interests and motivators of key decision-makers.
  • Demonstrate a strong focus on exceptional service to both clients and candidates.
  • Demonstrate well-developed presentation skills including both verbal and written communication skills.
  • Demonstrate a strong commitment to a team environment.
  • Demonstrate strong problem-solving and negotiation skills.
  • Proficient at handling difficult client negotiations with professionalism and respect.
  • Maintain courteous, professional, and effective working relationships with employees at all levels of the organization.
  • Develop, mentor and train assigned recruiters

Required Qualifications:
  • Bachelor’ s degree or equivalent sales/recruiting experience
  • 3+ years of professional outside sales experience in a staffing agency with focus on either an IT or Scientific
  • MS Office experience, including Word, Excel, and Outlook
  • Must be a self-starter who is highly self-motivated to not only meet goals and expectations but to exceed them
  • Exhibit an entrepreneurial mindset and professional image
  • Exhibit strong drive for results and success; convey a sense of urgency to achieve outcomes and exceed expectations; persist despite obstacles, setbacks and competing influences.
  • Quick learner, flexible and adaptable to the changing demands of the business
  • Must have the ability to thrive under pressure to meet hard deadlines
  • Must have a desire to learn and advance in a fast-paced sales environment and excel in a rewards driven culture based on performance
     

Preferred Qualifications:
  • Ability to build and proactively maintain working relationships with a network of technical professionals
  • Strong organizational and negotiation skills
  • Ability to develop and execute on recruiting strategies
  • Strong interpersonal skills to navigate workflow between the recruiting team, candidates and clients.
]]>
Mon, 21 May 2018 00:00:00 PDT 0
<![CDATA[Technical Recruiter]]> Bayside Solutions is seeking a talented, results driven Recruiter to be a part of our high-growth organization.  This is a unique opportunity to join a growing team of business professionals focused on building a first in class market-leader in technologies staffing and consulting services.

A successful Recruiter will thrive in a fast-paced environment, have a willingness to do attitude and possess an entrepreneurial spirit.  They also must have an amazing ability to build great relationships both internal peers and business partners as well as externally, with candidates and clients. 

The career of a Recruiter at Bayside Solutions is rewarding, challenging, prosperous and holds ample opportunity for professional growth. Bayside Solutions offers many career path options and a chance to develop an array of skills. Having been recognized as one of the Bay Area’ s fastest growing private companies, we' re ready to provide you with a challenging and rewarding career.

We believe our success here at Bayside Solutions is a direct reflection of the quality of talented people we hire and develop. New hire training is conducted on a one-on-one basis and covers: recruiting, career consulting and extensive recruiting skills. At Bayside Solutions we make a strong effort and commitment to provide all the tools necessary to ensure the success of every Recruiter.
 

Our Company Bio:

Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

 

Job Benefits:
  • An opportunity to join one of the fastest growing private companies in the area, with many possibilities for promotion and career growth
  • Upon receipt of direct hire status, you will be eligible for benefits including medical, dental and vision care, paid time off and holidays totaling more than 20 days a year
  • A competitive base salary and commission structure based on revenue generated
  • On the job training with an impressive success rate (more than 50% of our recruiters had no previous industry experience)


 

Summary of Responsibilities:

This position entails identifying excellent candidates to fill job requirements requested by our clients.

You will develop recruiting skills, including but limited to: generating a high call volume to produce a quantity of potential candidates, quickly and thoroughly screening candidates to learn about the person behind the resume, and maintaining relationships with hundreds of potential candidates. You will need to have excellent communication skills, must be able to build strong relationships quickly and demonstrate a drive to succeed.
  • Source and qualify resumes of industry professionals to identify potential candidates
  • Conduct in-depth phone interviews to recruit potential candidates in various markets that fit the needs and demands of our clients, both technically and culturally
  • Conduct in-person screens and interviews of potential candidates
  • Seek to understand the candidate’ s business drivers and motivations for exploring new opportunities.
  • Prospecting and negotiating contracts with candidates to use our placement services and building a supply of potential contractors
  • Consulting candidates throughout the entire interview process
  • Build and maintain on-going relationships with qualified potential candidates in various different markets.

Required Qualifications:
  • Bachelor’ s degree or equivalent experience
  • 1+ years of professional experience with a focus on customer service in a team oriented environment
  • MS Office experience, including Word, Excel, and Outlook
  • Highly self-motivated to not only meet goals and expectations but to exceed them
  • Quick learner, flexible and adaptable to the changing demands of the business
  • Must have the ability to thrive under pressure to meet hard deadlines
  • Must demonstrate the ability to work in a fast-paced, team-centric environment
  • Exceptional ability to multi-task and possess prioritization skills
  • Excellent verbal and written communications

?Preferred Qualifications:
  • Ability to build and proactively maintain working relationships with a network of technical professionals
  • Strong organizational and negotiation skills
  • Ability to develop and execute on recruiting strategies
  • Strong interpersonal skills to navigate workflow between the recruiting team, candidates and clients.
]]>
Mon, 21 May 2018 00:00:00 PDT 0
<![CDATA[Medical Writer I]]> Bayside Solutions is seeking a Medical Writer I  to be part of our client’ s team in South San Francisco. This is an opportunity to work with one of the largest Biopharmaceutical companies in the world developing innovative medicine to save patients’ lives.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Medical Writer I

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Cursory literature review of clinical trials publications (Conference abstract, publication) and clinical guidelines in Small Cell Lung Cancer with a focus on patient-reported outcomes, PhD.
  • Medical writing, data review and analyses, presentation, participation in global multi-functional teams.
  • Interactions with writing team to front load deliverables (CSR, AED) for non-data driven content and ultimately data-driven content.
  • Data interpretation (including use of interactive tools SPOTFIRE and R-SHINNY), summary and communication of the results.
  • Writing PRO-sections for CSR and AED.
  • Abstract and draft manuscript.
  • Create and maintain FORM contractor training manual.
  • Assist with preparation of presentations for internal leadership meetings.
  • Ensures resources are organized and stored appropriately.

Summary of Qualifications:
  • An advanced degree in psychology, health services research, public health or related discipline.
  • Industry experience, GCP/ICH guideline and practice exposure skills and experience in biostatistics (analyses of clinical trials data) and rating scales (patient-reported questionnaires) including descriptive analyses, cross-sectional and longitudinal modeling.
  • Proficient in medical writing.
  • Fluent in English (written and oral communication) with previous experience publishing data or writing clinical study reports.  
  • Experience in oncology preferred. 
  • Experience with Sportfire would be a plus.
]]>
Wed, 16 May 2018 00:00:00 PDT 0
<![CDATA[Business Analyst]]> Bayside Solutions is seeking a Business Analyst to be part of our client’ s team in Santa Clara. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Business Analyst:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Eliciting, analyzing and documenting all product requirements, business processes, and system requirements.
  • Work collaboratively with product owner, development team, lead architect and the development lead to assess current capabilities and identify high level customer needs.
  • Identify and author use cases and user stories.
  • Elicit requirements using interviews, document analysis, requirements workshops, storyboards, surveys, site visits, business process descriptions, use cases, scenarios, event lists, business analysis, competitive product analysis, task and workflow analysis, and/or viewpoints.
  • Write requirements specifications according to standard templates, using natural language simply, clearly, unambiguously, and concisely.
  • Decompose high-level business and user requirements into functional requirements and quality, specified in an appropriate level of detail suitable for use by those must base their work on the requirements.
  • Define quality attributes, external interfaces, constraints, and other nonfunctional requirements.
  • Set up and maintain the traceability from customer requirements to product requirements, functional design and verification.
  • Work with the architects, technical leads and the product owners to define the metrics and performance goals for the application.
  • Participate in the transitioning and communicating requirements and user stories to the designers and developers, and ensure a clear and complete understanding of the requirements.
  • Assist in translating the user stories and use cases into test conditions and the desired results for product, performance, and user acceptance testing.
  • Participate in reviews of the design, prototypes, and other work products to ensure they fully meet the requirement specifications.
  • Work collaboratively with the product owners to prioritize requirements and system tradeoffs to help make decisions and communicate trade-offs and risks.

Summary of Qualifications:
  • B.S. or B.A. degree in Computer Science, Engineering or related field.
  • Five years of experience in software development, including 3-5 years of practical professional experience in requirements engineering or business analyst.
  • Interviewing skills, to talk with individuals and groups about their needs and ask the right questions to surface essential requirements information.
  • Working knowledge of BDD methodology.
  • Listening skills, to understand what people say and to detect what they might be hesitant to say.
  • Analytical skills, to critically evaluate the information gathered from multiple sources, reconcile conflicts, decompose high-level information into details, abstract up from low-level information to a more general understanding, distinguish presented user requests from the underlying true needs, and distinguish solution ideas from requirements.
  • Facilitation skills, to lead requirements elicitation workshops.
  • Observational skills, to validate data obtained via other techniques and expose new areas for elicitation.
  • Writing skills, to communicate information effectively to customers, marketing, managers, and technical staff.
  • Organizational skills, to work with the vast array of information gathered during elicitation and analysis and to cope with rapidly changing information.
  • Interpersonal skills, to help negotiate priorities and to resolve conflicts among project stakeholders (such as customers, product management, and engineering).
  • Modeling skills, to represent requirements information in graphical forms that augment textual representations in natural language, including using modeling languages already established in the development organization.
  • 2-3 years of experience with Agile Scrum or Kanban development methodologies.
]]>
Tue, 15 May 2018 00:00:00 PDT 0
<![CDATA[Lab Technician - Operations]]> Bayside Solutions is seeking a Lab Technician - Operations to be part of our client’ s team in Branchburg, New Jersey. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Lab Technician - Operations:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Formulating enzyme Bulks, enzyme Reagents, Oligo Pools, Liat’ s oligo solutions, Buffer solutions, Protease production and HPLC eluent solutions by following. detailed instructions outlined in production batch records and SOPs.
  • Organize work to ensure efficient utilization of time and materials and to complete all procedures in a cGMP compliant manner.
  • Respond effectively to multiple and changing priorities, rescheduling work effectively to ensure that current and future needs are met.
  • Accurately and consistently record methods, materials, and results in batch records according to established formats and to keep supervisor informed on status of all projects and of significant findings and results in critical areas.

Summary of Qualifications:
  • B.S. in Chemistry, Biochemistry or other scientific discipline is preferred. 
  • Experience working in a laboratory and/or manufacturing environment is desirable. 
  • Good communication and teamwork skills are required.  
  • Ability to work under cGMP guidelines, and coordinate/implement production schedule is necessary. 
  • Strong verbal/written skills are required.
  • Knowledge & ability to work with chemicals, including solvents.
  • Comfortable working in a manufacturing/laboratory environment and wearing protective clothing for extended periods. 
  • Good documentation skills, including ability to write clear and legibly.
  • Organized, neat, conscientious, and flexible.
  • Duties may include handling of hazardous materials.
  • Manages schedules, workload and establishes priorities using inputs from business requirements, SAP, and/or internal customer needs. 
]]>
Tue, 15 May 2018 00:00:00 PDT 0
<![CDATA[Lab Technician - Operations]]> Bayside Solutions is seeking a Lab Technician - Operations to be part of our client’ s team in Los Gatos. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Lab Technician - Operations:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Perform and oversee production and production support duties for Operations and ensure quality of production and lab testing processed by the department. 
  • Performs a variety of duties relating to production and testing operations. Follows departmental work instructions, SOP’ s, OSHA safety regulations and cGMPs to perform assigned tasks. 
  • Monitor and oversee lab supply inventory, generate expense purchase requisitions, if applicable, input production data and other work-output data into appropriate network (e.g. SAP / LIMS) and maintain documentation in accordance with established procedures. 
  • Duties may include handling of hazardous materials in activities described above. Depending upon area of assignment or primary focus, may maintain departmental stock rooms, keep labs stocked, prepare buffers as needed/required which may also include performing direct production or testing activities. 
  • Monitor lab supply inventory, generate expense purchase requisitions, if applicable, input production data and other work-output data into appropriate network (e.g. SAP / LIMS) and maintain documentation in accordance with established procedures. 
  • Duties may include handling of hazardous materials as described above. Depending upon area of assignment or primary focus, may perform various manufacturing and testing duties in addition to maintaining departmental stock rooms, log books, preparing buffers as needed/required which may also include, performing direct manufacturing activities such as bulk formulation, filling, sub-assembly and sample testing.
  • Interface with internal groups to assure laboratory equipment maintenance, calibration and documents conform with established practices.
  • Attends required training classes and participates in on-the-job training. 
  • Manages schedules, workload and establishes priorities using inputs from business requirements, SAP, and/or internal customer needs. 
  • Participates in the design and organization of experiments in conjunction with supervisor. Providing input in writing experimental protocols, investigations and reports may be required.  Serves as a resource to operations or scientific staff.
  • Provides input for improving existing laboratory procedures.  Assist supervisor in development and implementation of new procedures and evaluating new products and equipment. Assist with generation of written standard operating procedures.

Summary of Qualifications:
  • Associates Degree or equivalent combination of education and work experience, Bachelor’ s degree preferred.
  • 2 - 4 years of relevant industry experience.
]]>
Tue, 15 May 2018 00:00:00 PDT 0
<![CDATA[Senior Software Engineer (C++)]]> Client Industry: Information Technology

Location: San Diego, CA / Campbell, CA

Position: Senior C++ Developer

Duration: 6 months contract to hire

About Us: Founded in 2001, Bayside Solutions was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

About the role: Our client is looking for Senior C++ Developer to join their team on a 6 months contract to hire. The position is open for hire either in San Diego or in Campbell, CA. This role requires strong collaborative and communication skills along with advanced skills in C++ development.

Qualifications:
  • Ability and desire to quickly evaluate and learn new concepts, technical skills and technologies.
  • Strong troubleshooting and problem solving skills.
  • Able to mentor others and lead design efforts.
  • Experienced in an agile development environment (Scrum, Kanban).

Must Have Skills:
  • 10+ years’ experience of recent C++ experience in Linux/Unix environment with strong understanding of STL and Boost libraries.
  • 5+ years of application design and development experience with XML, SOAP, HTML, web and restful services and technologies.
  • 5+ years RDBMS experience (e.g. Oracle 11g, SQL Server 2008 or later, MySql), with demonstrated ability to implement tables, views, triggers, procedures, functions, indexing.  Experience with document based databases a plus.
  • Experience with scripting languages such as Python and JavaScript.
  • Server side business and data access logic.
  • Ability to refactor individual functions when necessary.
  • Well versed in object oriented design, analysis, and development.

Desired Skills:
  • RogueWave experience.
  • Java development experience.

Education:
  • Bachelor’ s Degree or above (Computer Science, Bio Engineering, Electronics and Electrical Engineering or any related field).
]]>
Mon, 14 May 2018 00:00:00 PDT 0
<![CDATA[Senior Java Engineer]]> Client Industry: Information Technology

Location: San Diego, CA / Campbell, CA

Position: Senior Java Engineer

Duration: 6 months contract to hire

Summary of Duties:

As a Senior Java Engineer, you should be able to communicate effectively with your peers. Proven abilities in expressing ideas and concepts for the creation and self-maintenance of documentation is key to the role. The ideal candidate in this positions must have experience with the complete software development lifecycle which encompasses gathering requirements, writing design proposals, implementation, testing and maintenance and enhancement of both existing and new products. As a Senior Engineer, you will provide technical support and guidance to project team members and mentor associate developers.

Qualifications:
  • Great interpersonal skills and cross team collaboration skills are required
  • Must have the ability to communicate with technical and business stakeholders
  • Stay abreast of emerging technologies and software development best practices
  • Have the ability and eagerness to quickly evaluate and learn new concepts, technical skills and technologies
  • Serve as a mentor to others and lead design efforts
  • Lead the complete SDLC

Must Have Skills:
  • 10+ years’ experience with Java technologies (including Spring and Hibernate)
  • Linux experience (medium to advanced knowledge) is required
  • Experience working in an enterprise level environment
  • Experience with JSON, RESTful web services and client-server interactions
  • Experience  with highly scalable web services
  • RESTful API design and development
  • Experience with Oracle database

Desirable Skills:
  • Experience with Groovy and Scala
  • Experience with Spring Boot
  • Environment management/orchestration systems (Kubernetes, etc.)
  • Experience with testing frameworks and code quality tools
  • Experience with continuous integration environment and tools
  • Enterprise data warehousing design and development

Education:

Bachelor’ s Degree or above (Computer Science, Bio Engineering, Electronics and Electrical Engineering or any related field)  
]]>
Mon, 14 May 2018 00:00:00 PDT 0
<![CDATA[Equipment Technician II]]> Bayside Solutions is seeking an Equipment Technician II to be part of our client’ s team in South San Francisco. Imagine yourself collaborating with an organization focusing on the discovery, development, manufacturing, and commercialization of medicines to treat patients with severe or life-threatening medical conditions.

Our Company Bio:  Founded in 2001, Bayside Solutions is one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four-plus years and over 95% repeat business.

Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success!

You can find additional information on our company website at www.baysidesolutions.com.

Equipment Technician II

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Responsible for EQ in gASAT, which include end-to-end process of equipment qualification, maintenance, inventory management, change record and documentation.
  • Ensure compliance, data integrity and efficient EQ operation, develop and maintain business process.
  • Join the cross-functional and cross-site QC automation effort and lead the automation instrument qualification and database management sub team.
  • Serve as QC network expert for QC robot qualification and script/data management Representing gASAT in global data integrity team and EQ related CAPAmeetings or other compliance improvement effort.
  • Plan, coordinate, execute and document qualification of gASAT equipment and associated software compliance with GMP requirement.
  • Generate System Requirement Specifications, User Requirement Specifications, System Impact Assessments, and Component Function Criticality Assessments
  • Perform Quality Risk Assessments Coordinate with various functions within gASAT for priority and timelines of equipment qualification Write IQ/OQ/PQ protocols Execute IQ/OQ/PQ per protocols and write qualification reports Manage instruments inventory and PM schedule through SAP Set up an efficient system for performance maintenance tracking, scheduling and coordination Identify and propose resolution for validation deviations and discrepancies.
  • Design and execute quality investigations and CAPA (corrective actions preventive actions) initiatives as needed Identify resolution to technical problems; lead troubleshooting in equipment qualification and calibration activities.
  • Represent EQ function during internal and external audits and regulatory inspections. Responsible to addressing questions from audit inspection Ensure the EQ team meets schedules and timelines.
  • Operate within the relevant quality computer systems e.g, SAP ensuring implementation in line with quality and timeliness objectives

Required Qualifications
  • B.A. or B.S. degree (preferably in relevant scientific discipline) or an equivalent combination of education and experience and CAPA certifications.
  • Candidate must have strong track record in successfully leading EQ function with limited direction EQ or operating experience with automatic QC robot such as Tecan or Hamilton is highly desirable.
  • Previous hand on experience in analytical, cell based and PCR instruments and their qualification in GMP environment, and change control record is highly desirable.
  • Excellent resource and task planning and prioritization skills with the ability to deliver high quality results per planned timelines.
  • Knowledge of scientific theories, principles, techniques, used in analytical or biological/microbiologic test procedure.
  • Knowledge of and experience with cGMP, compliance, and regulatory requirements for biopharmaceuticals are required.
  • Experience with Labware LIMS, Trackwise, Change Control and other quality systems is desirable.
  • Strong written and verbal communication skills with proven record in protocol, report and deviation/CAPA writing.
  • Highly motivated and self-driven individual with the ability to work with minimal supervision to schedule, track, review, and report progress.
  • Familiarity with GMP requirements and compliance, high attention to detail and good documentation practices.
  • Consistently and independently exercises sound judgment, reasoning and problem solving.
  • Capable of working under minimal supervision and determining own short term priorities.
  • Basic knowledge of scientific theories, principles, techniques, used in analytical or biological/microbiologic test procedures.
]]>
Fri, 11 May 2018 00:00:00 PDT 0
<![CDATA[QC Support Analyst 4]]> Bayside Solutions is seeking a friendly, energetic and hardworking QC Support Analyst 4.This position is responsible for providing automation engineering function on all automated systems on site.

A successful Manufacturing Tech must be a strong team player, and provides a great attitude to the team.  They are one who is organized, diligent and provides positivity to the work environment.

The culture is based on the idea of others. They pride themselves in their commitment to finding cures that other biotech companies have not tackled.

Our Company Bio: 

Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

QC Support Analyst 4

Summary of Duties:
  • Performs routine testing including release testing, performance testing, analytical testing, bioburden testing, environmental monitoring using GMP/GLP practices.
  • Performs data analysis and results interpretations comparing to specifications, validity criteria, alert limits.
  • Responsible for maintaining product and QC material inventories.
  • Responsible for the maintenance and cleanliness of the laboratory, stocking shelves/drawers with testing materials.
  • Responsible for the maintenance and cleanliness of equipment, calibrating or submitting items for calibration as needed.
  • Responsible for completing training in a timely manner and maintaining the records.
  • Responsible for revising QC documents (SOPs, QSs) Participates in Lab Investigations and Out of Specification investigations.
  • Responsible for training QC analysts on test methods.
  • Participates or leads a QC department team.

Required Skills:
  • Minimum requirement of a Bachelor’ s Degree.
  • Working knowledge of GMP/GLP.
  • Intermediate computer skills.
  • Attention to detail.
  • 3-5 years of relevant experience.
  • QC experience in an FDA regulated environment is highly desirable.
  • LIMS experience helpful.
]]>
Thu, 10 May 2018 00:00:00 PDT 0
<![CDATA[IT Project Manager IV]]> Bayside Solutions is seeking an IT Project Manager IV to be part of our client’ s team in South San Francisco. Imagine yourself collaborating with an organization focusing on the discovery, development, manufacturing, and commercialization of medicines to treat patients with severe or life-threatening medical conditions.

Our Company Bio:  Founded in 2001, Bayside Solutions is one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four-plus years and over 95% repeat business.

Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success!

You can find additional information on our company website at www.baysidesolutions.com.

Project Manager IV

Summary of Responsibilities
  • Provides project management and business analysis for various applications requiring customer input using meeting facilitation to determine needs and develop solutions.
  • Can concurrently manage 1 – 3 projects of diverse scope across functional areas.
  • Manages projects using the corporate IT Project Management Methodology (PMM) lifecycle.
  • Creates and/or assists with required project documentation practices such as user requirements, functional specifications and testing plans.
  • Directs BSAs, Developers and SQA resources in the creation, testing and delivering of applications to support business requirements.
  • Manage a project team of approximately 15 people.
  • Manages project budgets of 1 million, scheduling, planning and contractor resource assignment and track vendor and resources’ performance including billing against budget and contract.
  • Manage project statements of work (SOW), change requests, requests for proposal and other procurement activities in conjunction with IT planning teams as required.
  • Effectively communicates to stakeholders in verbal and written form.
  • Collaborates effectively with business, technical and validation resources, to ensure project delivery and on-going support of business services and applications.
  • Interact and influence local and global teams and stakeholders.
  • Report and interact with directors and executives.

Required Qualifications
  • BS or BA degree in Business, Information Systems or engineering discipline.
  • PMI PMP certification or equivalent preferred.
  • 7 years of project management experience.
  • A professional focus on solution delivery and customer-service.
  • Ability to organize, prioritize and effectively manage multiple projects with various scopes simultaneously.
  • Ability to navigate between local and global teams, communicating and influencing accurately.
  • Excellent verbal and written communication skills with ability to manage vendors, project teams and stakeholders at all levels, including directors and executives.
  • Advanced ability with office productivity tools (Microsoft Office Suite, Google Apps, MS Project).
  • Demonstrated success handling initiatives of high complexity and risk.
  • Previous experience working in life sciences or drug development preferred.
]]>
Mon, 07 May 2018 00:00:00 PDT 0
<![CDATA[Senior/Staff Software Engineer]]> Position: Senior Software Engineer

Location: Boulder, CO

Terms: Full time hire

About Us: Founded in 2001, Bayside Solutions was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

About the role:

Our client is a Biotech start-up and has a very lean development team. They are looking to bring in a Senior Software Engineer as a direct hire to help them scale up and grow the team. This resource will be responsible for providing guidance and mentoring junior associates on the team. The ideal candidate will have a strong mathematical background and must be an excellent communicator.

Responsibilities:
  • Creating and maintaining custom information management systems software (primarily written in Java and C#) to track process data and workflow queues
  • Developing new software/systems to support delivery of data to customers,
  • Creating/maintaining/tuning database SQL required to support the system functionality and other database centric applications used internally
  • Mentoring junior software engineers and database developers
  • Supporting end-users in a 24/7 production environment as needed
  • Such other matters as may be determined by yourself and the Company

Qualifications:               
  • Recent success in a start-up environment.
  • 10+ years’ experience with OOP using Java, C# and/or C in a client/server architecture.
  • Experience with developing complex custom web GUI and visual components on a web platform – AngularJS preferred.
  • Must have advance skills in writing complex SQL queries, optimizing stored procedures and data table performance - MSSQL preferred.
  • Understanding of laboratory processes and workflow systems is a plus.
  • Ability to manage daily test processing needs with high emphasis on quality.
  • Ability to work as part of a team.
  • BS in Computer Science, Engineering or Life Sciences is preferred
]]>
Fri, 04 May 2018 00:00:00 PDT 0
<![CDATA[Salesforce Tech Lead]]> Position:  Salesforce  Developer / Technical Lead

Client Industry: Health and Wellness

Location: East Bay

Terms: Full Time 

About Us:  Founded in 2001,  Bayside  Solutions has been recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success. 

Our client in East Bay is looking to add a  Salesforce  Technical Lead to their growing team. This is a full time opportunity. 

About the opportunity:

Our client has a very lean team and is moving from old school solutions towards cloud based services and digital experiences. This role is unique since this individual will be responsible for having in depth technical knowledge of the implementation of Service Cloud and Partner Communities. As a Technical Lead, you will be required to code at least 50% of the time and lead an offshore development team.  You will be responsible for developing and enhancing the system to meet business requirements and responding to production issues on priority. 

Responsibilities:
  • Lead the  Salesforce  offshore development team.
  • Proven skills in technical design analysis.
  • Responsible for delivering clean, quality code that meets defined standards.
  • Leverage comprehensive understanding of  Salesforce  products and platform to provide technical recommendations on solutions and enhancements.
  • Responsible for configurations and  customizations  for  Salesforce  in stage and production environments.
  • Customize and manage profiles, roles, security settings, sharing rules, custom objects, custom fields, page layouts,  workflow, validation rules, approvals, etc.
  • Develop or enhance custom objects, Visual Force pages, APEX classes, triggers and services, reports, dashboards, and  workflows.
  • Administration of the  Salesforce  instances, manage fields/relationships,  workflow  rules, approval processes, page layouts, security, validation rules, email notifications, custom buttons/links, etc.
  • Develop reports, dashboards, and processes to continuously monitor data quality and integrity.
  • Respond to production severity issues with required intensity of attention.
  • Ensure data security is enforced by the use of roles, profiles, and sharing rules.
  • Perform unit testing and fix any defects. Support the user acceptance test activities.
  • Develop and manage the release process.
  • Prepare project documentation including technical specifications and unit test scripts. 

Requirements:
  • At least 5+ years experience in  Salesforce  development (including Lighting, Apex,  SOQL,  Visualforce, web service  APIs, JavaScript, and  CSS)
  • In-depth understanding of the  Salesforce  platform
  • Experience with Partner Communities and Service Cloud required.
]]>
Thu, 03 May 2018 00:00:00 PDT 0
<![CDATA[Sr. Research Associate - Protein Sciences]]> Bayside Solutions is seeking a Sr. Research Associate – Protein Sciences to be part of our Client’ s team in San Francisco. Our client is seeking a talented and motivated team member to support our research efforts in developing our antibody-based immuno-oncology therapeutics.

Our Company Bio:  Bayside Solutions was founded in 2001, and was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Sr. Research Associate – Protein Sciences

Job Benefits:
  • An opportunity to join a company focused on delivering targeted, science-based biological products to improve crop productivity.
  • Work for a company that is local to the bay area, in the beautiful South San Francisco area.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Development of biosensor (SPR or BLI) based assay platforms for screening/characterization of antibody binding and specificity
  • Biophysical characterization of antibody stability and developability assessment using calorimetry (ITC, DSC), light scattering, and differential scanning fluorimetry (DSF) to support lead candidate selection
  • Organization and analysis of results, communicating and presenting findings in team meetings, and contributing to scientific publications
  • Troubleshooting and optimizing assays through data interpretation, identification of novel or alternate procedures and techniques, and timely execution
  • Ability to work in a team environment and adapt to changing company priorities

Required Qualifications:
  • Bachelor’ s or Master’ s degree in a life sciences discipline with at least five plus years of industry experience in developing assays using SPR, BLI, DSC, DSF, FTIR, AUC, and DLS
  • Good understanding of biophysical characterization of antibodies is must
  • Experience in standard protein analytical techniques including electrophoresis, Western Blot, ELISAs, HPLC, UV-Vis spectrophotometry
  • Proficiency in protein production and purification techniques (e.g., using peristaltic pumps, HPLC systems), ultrafiltration/diafiltration is a significant plus
  • Motivation to learn and use new and emerging techniques for mammalian cell culture, protein production, flow cytometry, and gene manipulation in cells
  • Excellent communication skills with the ability to work effectively in a dynamic and flexible team environment
  • Ability to maintain detailed records of experimental methods and results
  • Ability to critically interpret and effectively present data
  • Adaptability to shifting priorities and changing work assignments
]]>
Wed, 02 May 2018 00:00:00 PDT 0
<![CDATA[Manufacturing Associate II, III (Day)]]> Bayside Solutions is seeking a Manufacturing Associate to be a part of our partner’ s team in the San Francisco East Bay Area. This is an opportunity to work with a Biotechnology company focused on providing fast acting therapeutic relief through a proprietary transdermal system.

 

Our partner’ s culture is fosters creativity, execution, accountability, urgency, and transparency. These are aspects of that are essential for establishing a robust portfolio of products that they have in development.

 

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.
 

You can find additional information on our company website at www.baysidesolutions.com.

Manufacturing Associate

Job Benefits:
  • An opportunity to join a biotech utilizing current drugs for their fast acting transdermal applications
  • Work for a company that is local to the bay area and recognized as a leader of innovation
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K

 

Summary of Responsibilities:
  • Support manufacturing set-up, operation, troubleshooting and dismantling equipment used for the preparation of drug delivery systems.
  • Provide support for process and equipment validation activities for cGMP operations.
  • Demonstrate ability to recognize and document equipment malfunctions and process deviations.
  • Assist with resolving technical issues as well as maintenance of production equipment.
  • Follow SOPs and complete master production records in a cGMP environment.
  • Complete and Review batch production records to ensure cGMP documentation practices are followed and information entered is complete and accurate. 
  • Provide communication between shifts to ensure smooth and efficient transition of tasks.
  • Bring equipment and facilities issues to the attention of the Supervisor for resolution. 

 

Required Qualifications:
  • BS with one years’ experience or equivalent years’ experience the medical device field or Pharmaceutical/Biotech industry. 
  • Aseptic manufacturing experience is highly desired.
  • Experience with gowning up procedures and protocols.
  • Experience in classified clean room manufacturing operations is required.
  • Perform duties in accordance with Current Good Manufacturing Practices (cGMP’ s), FDA and ISO guidelines.
  • Strong mechanical aptitude and familiarity or experience in handling drug compounds, organic chemicals and solvents is required. 
  • Demonstrated basic math skills.
  • Able to sit or stand for long periods of time. 
  • The ability to lift 35-40 lbs. is essential.

 
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Wed, 02 May 2018 00:00:00 PDT 0
<![CDATA[Network Analyst I]]> IT/Network Administrator

Client: Healthcare

Location: Concord, CA

Duration: Contract to Hire

 

Join Us

Bayside Solutions is an industry-leading provider of staff augmentation and consulting services. Since 2001, we' ve built our company around a single concept - relationships. We focus on the people we serve. We' re straightforward, consistent and 100% accountable. We deliver intelligent solutions that help our clients and candidates thrive.

 

The Role

We are looking for a talented Network Administrator to join our Healthcare client. This person will be performing a full range of system administration activities for computer network with mini-computers and multiple Local Area Networks (LAN' s) and Wide Area Networks (WAN' s).

 

Deliverable
  • Monitors and enhances complex computer and communications systems, on-site or remote; develops, designs and implements problem solutions, using standard analysis techniques; and recommends solutions to correct malfunctions
  • Installs and configures computer and/or telecommunications hardware and software; and services and maintains equipment
  • Designs, develops and implements computer applications for user departments
  • Administers remote logins, system securities, data transfers, and remote activities
  • Retrieves and downloads/uploads data and assists with transitioning data/operations between systems
  • Maintains systems back-ups and control records; assists in the maintenance of files and libraries; creates logical directory structure; and may be responsible for retention and storage of databases
  • Capacity planning, technology planning, disaster planning and budgeting required to ensure an efficient, effective, and reliable system
  • Directs and coordinates the design, development, acquisition and implementation of computer hardware, software and data communications solutions that will meet the needs of the division
  • Project management and change control for all internal system and component changes
  • Performs system and user account creation, maintenance, security and removal
  • Monitors daily activity on systems, checking for potential problems, resource ability, performance and " load" characteristics, and network integrity; monitors systems activity and usage to maintain a secure environment; and troubleshoots, repairs and provides viable recommendations for resolving problems
  • Interfaces with department staff/customers to provide help with hardware or software related questions, network or connectivity questions, and general assistance required regarding the systems, software, and resources
  • Keeps current with software releases and updates for all operating systems, applications and e-mail systems, keeping all systems at current release levels, unless directed otherwise
  • Evaluates new software under consideration for adoption; reviews available public domain software for possible use; and maintains accurate inventory of licenses and appropriate version/release levels for all applications in use
  • Develops and maintains written and on-line documentation, procedures and help files which includes keeping existing documentation current as well as occasionally authoring end-user documentation
  • Interfacing with vendors' sales and field services personnel to coordinate normal periodic maintenance and arrange for and monitor equipment repairs and purchases

 

You Have
  • 4+ years of full-time professional experience in designing, installing and maintaining complex multi-site Network Server Operating Systems, and LANs using physical layers, bridges, and routers.
  • On-site broad-based technical, operational, programming and analytical problem-solving support Installation, maintenance, expansion, and upgrading of software, hardware, networks and peripherals common operating systems

 

 
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Thu, 26 Apr 2018 00:00:00 PDT 0
<![CDATA[Scientist, Study Coordinator]]> Bayside Solutions is seeking a Study Coordinator to be a part of our partner’ s team in the San Francisco South Bay Area. This is an opportunity to work with a startup Biotechnology company focused on providing therapeutics for gastrointestinal diseases.

Our partner’ s culture is fast paced and passionate about innovative drug discovery and development.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

 

Study Coordinator:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.


Summary of Responsibilities:
  • The individual is a self-starter with excellent study management capabilities and is a critical part of an innovative team that to support the company’ s drug development process.
  • Coordinating with CRO Study Directors,  DMPK Group, scientists, formulation vendors, and/or analytical labs to design and carry out the studies.
  • Requesting quotes and looking for the best deals/timing from different CROs.
  • Writing/reviewing study protocols and amendments.
  • Shipping test articles that are prepared internally.
  • Tracking completion of each milestone of the study (protocol approval, shipment of TA, dosing, receipt of samples, receipt of data).
  • Managing CRO quotes.
  • Reviewing in vivo reports.
  • Monitor project progress and document the involved aspects of the projects, coordinate CROs and internal resources to make sure the projects are on schedule and the results are delivered on time.
  • Review the project protocols and amendments to ensure the scope and the direction of the projects.
  • Calculate the PK parameters for biological samples (such as plasma, urine, rectal feces and standard feces) using various software, determine the tissue distribution of our compounds, perform the data analysis, report data summaries and interpret results for project teams.
  • Review technical study reports and IB report.

                          
Requirements of Qualification: 
  • BS or MS degree in a biological science or a related field along with a minimum of 5 years of experience conducting toxicology studies in a biotech/pharma environment.
  • Experience in outsourcing, vendor management, and establishing and managing CROs driving timely delivery of clear, accurate, and well-written nonclinical study data. 
  • Strong verbal communication skills accompanied by scientific writing skills.
  • Enjoys and thrives in a fast-paced, multi-tasked, and hands-on environment

 
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Tue, 24 Apr 2018 00:00:00 PDT 0
<![CDATA[Enzyme Engineer Research Associate]]> Bayside Solutions is seeking an Enzyme Engineering RA to be a part of our partner’ s team in the Pleasanton Area. They are a gene editing technology company developing a family of CRISPR enzymes.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Enzyme Engineering RA

Responsible for the discovery and optimization of the enzymes that drive innovation.

Job Benefits:
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Construct high quality gene variant libraries and optimize protocols for library construction
  • Run assay processes for key phenotypes, including preparing samples for Next-gen sequencing
  • Work closely with automation engineers to execute these workflows on laboratory automation workstations
  • Provide general lab and data analysis support for an Enzyme Engineering Scientist

Required Qualifications:
  • B.Sc. in a life sciences related discipline
  • 2+ years of hands-on laboratory experience, preferably in an industry setting
  • Experience running and optimizing basic molecular biology protocols including PCR, DNA purification, transformation and DNA sequencing
  • Some familiarity with software and data tools such as Python, C++, SQL
  • Experience with laboratory automation is desirable but not a requirement
  • Desire to work in a team environment and collaborate closely with other cross-functional teams
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Thu, 19 Apr 2018 00:00:00 PDT 0
<![CDATA[Automation Engineer]]> Bayside Solutions is seeking an Automation Engineer to be a part of our partner’ s team in the Pleasanton Area. They are a gene editing technology company developing a family of CRISPR enzymes.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Automation Engineer

Responsible for developing and operating automation solutions in support of the Enzyme Engineering and Applications teams.

Job Benefits:
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Based on requirements gathered from Enzyme Engineering and Applications teams, assist in selecting, purchasing, installing and validating new automation equipment
  • Work closely with bench scientists to adapt protocols to automated systems and script new workflows that meet key performance metrics
  • Collaborate with scientific teams to execute these automated workflows
  • Perform equipment maintenance, calibration and quality assurance to ensure process robustness and minimize down time
  • Integrate automated workflows with internal software and data systems to automate complex experimental designs and ensure samples and metadata are captured and tracked appropriately

Required Qualifications:
  • MS or BS in a Science or Engineering discipline
  • 3 or more years hand-on experience with automated liquid handling systems such as Tecan Freedom Evo, Biomek FX/NX or Hamilton Vantage/Microlab.
  • Demonstrated ability to adapt bench-scale protocols to automation systems
  • Experience with relevant software and data systems such as Python, C++, SQL
  • A desire to work in a highly collaborative and cross-functional team
  • Ability to learn quickly in a fast-paced startup environment
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Thu, 19 Apr 2018 00:00:00 PDT 0
<![CDATA[Senior Analyst, Asset Liability Management]]> Position: Senior Analyst              

Location: San Francisco, CA

Client Industry: Banking

Terms: 6-12 months contract

Number of positions: 2

About Us: Founded in 2001, Bayside Solutions was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

About the role: Our client is looking for Senior Analysts with experience in Asset Liability Management for a 6-12 months contract. This is a high visibility role and strong communication skills with business acumen are a must have. These resources will provide expertise on a System Implementation on client site.

Key Responsibilities:
  • Assist in meeting monthly and quarterly Asset Liability Management risk assessment and reporting requirements by utilizing: Net Interest Income simulations, Economic Value of Equity, and other relevant analyses.
  • Play an integral hands-on role in the implementation, configuration, testing, and ongoing maintenance of an Asset Liability Management risk platform.
  • Develop and maintain various financial or forecasting/planning models used to project the operating results and risk exposure of the Bank under various macroeconomic and credit environments.
  • Support various groups within Finance and the Bank with relevant analyses of the impact of business decisions on the bank' s interest rate risk exposure, profitability and performance, capital ratios, regulatory requirements, and others.
  • Assist in the annual Dodd-Frank Act Stress Test analyses and submissions.

Qualifications:
  • Hands-on experience with Asset Liability Management
  • Experience with QRM, ALM5/6, or Empyrean
  • Skilled with SQL and VBA
  • Advanced understanding of valuations concepts (EVE)
  • Advanced skills in MS Excel
  • Proactive and positive attitude
  • Quick learner with strong analytical aptitude
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Fri, 13 Apr 2018 00:00:00 PDT 0
<![CDATA[Analyst, QC I]]> Bayside Solutions is seeking an Analyst, QC I  to be part of our Client’ s team in Marin County. This is an opportunity to work with a local Biopharmaceutical company focusing on the developing and commercializing novel therapies for rare diseases.  

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. Their company has been recognized as one of the fastest drug developers in the industry and has also been recognized among the Top 10 World’ s Most Innovative Company’ s in 2015 & 2016.Their organization is fueled by their employee’ s passion and dedication to change the course of disease.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Analyst, QC I

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Enjoy working in a team environment where feedback/interaction/collaboration is heavily encouraged.
  • Perform, under direct supervision, chemical analyses of incoming raw materials under cGMP to meet specified timelines.
  • Coordinate and track outside laboratory testing activities.
  • Maintain the laboratory in an inspection ready state.
  • Must have a quality service attitude and be willing to work additional hours to meet production or laboratory requirements when necessary.

Required Qualifications:
  • B.S./B.A. in Science (major in biology-biochemistry-chemistry or related field) with 1 - 2 years of relevant laboratory experience or A.S. with at least 2 years of relevant laboratory experience.
  • Must have a positive, team minded personality Experience working in a GMP laboratory Experience with physical and chemical methodologies and a variety of analytical instrumentation Organizational skills as well as good written and verbal communication skills essential.
  • Experience with Microsoft Word and Excel required; experience with Labware LIMS, O365 a plus.
  • On rare occasion, may be required to work overtime, weekends and holidays to meet deadlines and requirements.

 
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Tue, 10 Apr 2018 00:00:00 PDT 0
<![CDATA[Lead IT Applications Analyst (POS)]]> Role:                     Lead IT App Analyst aka Project Manager

Industry:              Retail

Location:             Dublin

 

Bayside Solutions is seeking a Lead IT App Analyst for our client in Dublin CA.  Areas of focus will be Project Management, Vendor Management, Information Management, Software Development, and TechOps

 

A successful candidate will be tasked with working on very significant and unique store system projects, assignments and issues. This person will also act freely to decide methods and procedures on new/special assignments and will lead/oversee the activities of others associates.  

 

Primary Responsibilities Include But Are Not Limited To:
  • Identify holes in existing functionality and review requirements with stakeholder’ s complex projects.
  • Develop high level functional design solutions.
  • Ensure designs abide by the architectural roadmap; support development/execution/operation of service complex projects.
  • Authenticate processes to guarantee that specific designs match and are traceable to requirements complex projects.
  • Must be influential and authoritative advising development team during design and build phases to safeguard quality deliverables are produced.
  • Drive test execution throughout all phases of testing
  • Create training deliverables: training plan, training schedule, job aids, etc.

 

Qualifications:
  • 8 years of experience in the IT field or equivalent work experience
  • Bachelor’ s Degree (required) or Master’ s Degree (nice to have) from a STEM related field.
  • Ability to act independently to determine methods and procedures on new or special assignments
  • Ability to create formal networks involving coordination among groups

 

Preferred Qualifications:
  • Very technically competent
  • Working experience with POS and payment processing systems
  • Programming experience with computer languages such as SQL, PL/SQL
  • Working experience with system configurations, file systems, network, and Store device
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Fri, 06 Apr 2018 00:00:00 PDT 0
<![CDATA[IT Applications Analyst (Store System)]]> Role:                     IT App Analyst in Store Systems

Location:             Dublin CA

Industry:              Retail

 

The IT App Analyst is responsible for application support as well as applying new or existing technologies and solutions to solve business needs.  A successful candidate may serve as a functional and/or technical expert in one or more disciplines.

 

Primary Duties Include But Are Not Limited To:
  • Manage technical staff that support current production systems as well as the creation of new systems
  • Assess technical designs, develop alternatives, and recommend appropriate solutions.
  • Collaborate with other IT and business teams, to maintain punctual and successful issue resolution.
  • Prepare estimates of technical project components.
  • Develop project plans covering the entire systems development life cycle.
  • Design, code, integrate, and implement solutions.
  • Participate in projects throughout the entire SDLC; create timely / thorough status reports and leading status meetings to maintain the following
    • Accurately defined requirements
    • Purchased, designed or coded systems meet requirements, and execute efficiently
    • System interfaces are successfully coded, designed and tested
    • Full cycle test and training plans are designed and executed appropriately
    • Calculate, track, and balance all financial responsibilities per project/task
    • All required system and user documentation is created accurately
    • Accurate system and user documentation
    • Successful and timely completion of all projects.

 

Requirements:
  • At least 5 years of experience in supporting IT systems.
  • Bachelor’ s degree (required) or Master’ s degree (nice to have) in a STEM related field
  • Analyzing and correcting system functionality problems
  • Ensuring the related fixes and/or enhancements are tested successfully (by IT and by key users)
  • Ensuring all support activities are executed on time and under budget
  • Identify alternative methods of application, performance and stability improvement
  • Experience working with Windows Operating Systems
  • Working experience with relational databases – specifically Microsoft SQL
  • Programming experience with computer languages such as SQL, PL/SQL, and Pro C
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Fri, 06 Apr 2018 00:00:00 PDT 0
<![CDATA[Pharmacovigilance Associate II]]> Bayside Solutions  is seeking a Pharmacovigilance Associate II to be part of our Client’ s team in Marin County. This is an opportunity to work with a local Biopharmaceutical company focusing on the developing and commercializing novel therapies for rare diseases. 

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. Their company has been recognized as one of the fastest drug developers in the industry and has also been recognized among the Top 10 World’ s Most Innovative Company’ s in 2015 & 2016.Their organization is fueled by their employee’ s passion and dedication to change the course of disease.

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Pharmacovigilance Associate II

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation. 
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Participates in activities related to, and processing of, Adverse Events for marketed products and investigational products.
  • Accountable for accurate data capture for individual case safety reports.
  • Responsible for narrative creation for individual case safety reports.
  • Perform quality review and submissions (as appropriate).
  • Ensuring departmental workflow processes and timelines are followed.
  • Proactively managing workload to ensure regulatory timelines are met.
  • Demonstrated knowledge of safety concepts and global regulatory reporting obligations

Required Qualifications:
  • Bachelor' s degree in a Life Science Degree Required
  • Minimum of 2-5 year previous Pharmacovigilance experience required.
  • Strong knowledge of medical terminology.
  • Strong organizational skills, detail oriented, ability to adapt to change.
  • Proven team player with the ability to function in a multi-disciplinary environment.
  • Demonstrates initiative and accountability.
  • Excellent communication skills, both verbal and written.
  • Computer literate

 
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Fri, 30 Mar 2018 00:00:00 PDT 0
<![CDATA[System Engineer (SCCM)]]> System Engineer (SCCM)

Company: Retail

Location: Dublin, CA

Principal Duties and Responsibilities include but are not limited to:
  • Develop and implement patch and vulnerability remediation process including package creation, testing and deployment.
  • Develop and optimize pre- and post- patching process to ensure proper implementation without any outages.
  • Coordinate patch schedule with other teams such as patch team, infrastructure management, security operations, governance & risk. Communicate project and operational metrics.
  • Assess software patches and create recommended patch list with logical explanation in terms of compliance.
  • Score each patch based on risks & opportunity to prioritize. Identify which patches are more valuable to the organization than others.
  • Assist in developing action plans, schedules, budgets, status and metrics reports as well as other management communications intended to improve the patch management program.
  • Thorough testing of patches in a non-Production environment. Must be able to think ahead to avoid business outages based on the lab results.
  • Assist in the process for vulnerability and patch management ensuring they are compatible with the company' s business needs and strategic objectives
  • Available for rotation assignment for on-call support duties

Qualifications:
  • 8 to 12 years’ experience supporting diverse IT systems, processes or capabilities
  • Must have excellent competency with SCCM, WSUS and other patching tools.
  • Must be able to create deployment patch package using SCCM and WSUS
  • Solid understanding of industry best practices for Patch Management; specific demonstrated experience mapping business processes and comparing those processes to industry best practices
  • Understanding of the balance between business and patch requirements
  • Proficiency in scripting of packaged installation of patches, software and configuration changes.
  • Must have understanding of network, system and application security
  • Knowledge of various vulnerability scanning solutions, scripting and automation
  • Experience with automation tool like Ansible, data base and Java application development (in-house developed or off-the-shelf) will be a plus
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Tue, 27 Mar 2018 00:00:00 PDT 0
<![CDATA[IT Applications Analyst]]> ROLE:                    IT Application Analyst

LOCATIONS:       Dublin CA

INDUSTRY:          Retail

 

Bayside Solutions is seeking an IT Application Analyst for our retail client in Dublin CA. 

 

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

 

PRIMARY SKILLS INCLUDE BUT ARE NOT LIMITED TO:
  • In the IT Allocation Department you will be responsible for designing, developing and implementing IT solutions.
  • Contribute in projects through the entire systems DLC making sure that requirements are accurately defined, that code meets defined requirements, and that test plans are planned and executed successfully.
  • Design, configure, and test changes to support business requests.
  • Provide Level 1 support for critical production issue resolution.

 

QUALIFICATIONS:
  • 3+ years of experience implementing and/or supporting JDA Allocation Systems.
  • Strong comprehension of Allocation business process generic to Retail industry.
  • Ability to interpret technical issues into business terms.
  • Experience implementing, supporting and troubleshooting interfaces using oracle PLSQL
  • Working experience in Linux/UNIX environment
  • Experience with shell scripting
  • Bachelors or Masters in a STEM related subject.

 

PREFERRED QUALIFICATIONS:
  • Planning reporting experience preferred
  • Experience with JDA Advanced Allocation
  • Experience in Hive SQL
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Mon, 19 Mar 2018 00:00:00 PDT 0
<![CDATA[Machinist]]> Bayside Solutions is seeking a Machinist to be part of our Client’ s team in Pittsburg.

Our Company Bio: 

Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Job Benefits:
  • Offers their full benefit package
  • Competitive compensation
  • This position is eligible for medical, vision, dental, life insurance, flexible spending account (FSA), pension plan, and 401K plan.

Summary of Responsibilities: 
  • Post-secondary education or experience needed to meet demands of the trade.
  • Ability to plan and layout work, interpret drawings and sketches while operating equipment at close tolerance

Must have professional knowledge and skills to work on the following equipment or systems:
  • Operate Milling Machines
  • Slitters
  • Planers
  • Drill Presses
  • Grinders
  • CNC
  • Lathes
  • Shapers
  • Boring Mills
  • Key Seater
  • Hydraulic Press

Required Qualifications:
  • High School Diploma or GED. Minimum experience in an industrial maintenance or operation environment.
  • Documented completion of technical or trade courses is a plus.
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Fri, 09 Mar 2018 00:00:00 PST 0
<![CDATA[Industrial Maintenance Mechanic]]> Bayside Solutions is seeking am Industrial Maintenance Mechanic to be part of our Client’ s team in Pittsburg. A successful Maintenance Mechanic will inspect, dismantle and repair all mechanical, hydraulic, and control systems to ensure proper operation.

Our Company Bio: 

Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Job Benefits:
  • Offers their full benefit package
  • Competitive compensation
  • This position is eligible for medical, vision, dental, life insurance, flexible spending account (FSA), pension plan, and 401K plan.

Summary of Responsibilities: 
  • Post-secondary education or experience needed to meet demands of the trade.
  • Ability to interpret mechanical drawings a schematics needed for maintenance and repair of plant equipment and machinery,
  • Also have the ability to learn the computerized recording system (MAXIMO).

Must be versed in all areas as noted below:
  • Hydraulics
  • Pneumatics
  • Print reading
  • Welding (MIG/TIG)
  • Power Transmission
  • Lubrication
  • Pumps
  • Piping
  • Mechanical Maintenance
  • Shop Machines, Tools, & Equipment

Required Qualifications:
  • High School Diploma or GED. Minimum experience in an industrial maintenance or operation environment.
  • Documented completion of technical or trade courses is a plus.
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Fri, 09 Mar 2018 00:00:00 PST 0
<![CDATA[Windows Operations Systems Engineer]]> Systems Engineer           

Industry: Financial Service

Duration: Contract to Hire

Location: San Mateo, CA             

Interview Process: Phone, Onsite

 

Join Us

Bayside Solutions is an industry-leading provider of staff augmentation and consulting services. Since 2001, we’ ve built our company around a single concept – relationships. We focus on the people we serve. We’ re straightforward, consistent and 100% accountable. We deliver intelligent solutions that help our clients and candidates thrive.

 

We Have
  • Install and Configure Microsoft Windows Server 2012 R2 and 2016
  • Troubleshoot and debug systems end-to-end
  • Manage technical support relationship with our financial software vendors.
  • Train, mentor and lead junior system support team members.
  • Utilizes design skills to define Technical Design Specifications for complex and high impact projects
  • Create, train and manage all necessary documentation including but not limited to system standards, run-books, etc.
  • Take ownership of new and/or existing environments including planning upgrades, staying on top of EOL dates and documenting inter-dependencies
  • Research software solutions to meet current business needs or to proactively create efficiencies
  • Participate in 24x7 on-call rotation

 

You Have
  • Bachelor’ s degree in MIS, computer science, math, or other related science field (or equivalent)
  • 5+ years of  experience in supporting an enterprise class infrastructure
  • Experience providing advanced level OS support for Microsoft Windows Server 2012 R2 and 2016
  • Experience supporting portfolio management, compliance, or trading infrastructures
  • Good knowledge of Financial Services systems such as Order Management Systems (OMS), FIX, TNS, market data providers and crossing systems.
  • Good understanding of Transaction Network Services for financial data communications and interoperability solutions
  • Understanding of controlled private networks which includes extranets and DMZs
  • Strong analytical capabilities.
  • Scripting experience using PowerShell and task automation
  • Ability to communicate with all levels of management and end users with varying levels of technical expertise

 

Competitive Advantage
  • Prior experience with servers build out from scratch
  • Prior experience and full ownership implementing and customizing systems software/applications
  • Prior experience working in a banking,  investment management or investment research firm
]]>
Fri, 09 Mar 2018 00:00:00 PST 0
<![CDATA[Sr. Research Associate]]> Bayside Solutions is seeking a Sr. Research Associate  to be part of our Client’ s team in San Jose. This position is for a self-motivated scientist with strong technical ability and demonstrated proficiency in performing troubleshooting complex cellular and molecular biology systems. Candidate  will help in developing and transferring our technologies for fast and low-cost genome sequencing.

The candidate should be able to effectively communicate, design and perform experiments independently with minimal supervision. The candidate should be dynamic and a good team player in a cross-functional environment.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Sr. Research Associate

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Develop and test novel concepts.
  • Follow verbal and written instructions.
  • Plan, run experiments, analyze, interpret and report results in a timely fashion.
  • Participate and contribute in weekly group meetings on experimental design, activity planning, and troubleshooting, including reporting experimental results.
  • Execute experimental work plans in collaboration with other group members, providing technical expertise, material and hands-on support as needed.
  • Perform other work-related duties as assigned.
  • Experience in a biology research laboratory.
  • Molecular biology experience including DNA, RNA isolation, quantification and purification, ligations, gel electrophoresis, primer design, RT-qPCR, cDNA preparation and genotyping.
  • Cell biology experience including cell isolation, flow cytometry, immunostaining, mammalian cell culture, microscopy.
  • Experience in DNA/RNA library preparation for NGS is desirable.
  • Familiarity with NGS, handling liquid biopsies, cell sorting and industrial experience will be a plus.

Required Qualifications:
  • Bachelors or Master’ s degree in Molecular and Cell Biology or related field with a minimum of 2-5 years of experience.
  • Should be well organized, motivated and possess excellent time management skills.
  • Ability to multitask and adapt to rapidly changing requirements, priorities and tight schedules.
  • Excellent analytical, organizational, and planning skills, with great attention to detail and record-keeping.
  • Effective communication and presentation skills.
  • Knowledge of S88 Batch Controls is a plus

 
]]>
Thu, 08 Mar 2018 00:00:00 PST 0
<![CDATA[Director of Information Security (CISO)]]> ROLE:                   Director of Information Security

LOCATIONS:       Martinez, CA

INDUSTRY:          Hospital and Healthcare

Bayside Solutions is seeking a highly practiced Director of Information Security (CISO) to be part of our client’ s security team in Martinez CAThe candidate will provide active leadership for security programs for our client that are designed to provide for the confidentiality, integrity, and availability of data, physical, and virtual assets.

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

Principal duties include but are not limited to:
  • Coordinates and directs as required technology and security efforts to maintain compliance with applicable Federal, State, Local and industry regulations
  • Maintains high compliance for system OS and application patching for assets within 6 weeks of patch release
  • Work with our client, the County, and Industry to deliver an operationally functional and secure technology platforms for services delivered by our client
  • Plans, organizes, schedules, and completes budgets, projects, and policies in an efficient, productive manner
  • Develops processes to secure externally hosted applications and data sets

Required Qualifications:
  • Bachelor’ s Degree (required) Master’ s Degree (preferred) in a STEM related field.
  • Honesty and Integrity is a critical competency and characteristic of any role. This is manifested by not cutting corners ethically, earns organization trust and maintains confidentiality.
  • Handles sensitive matters with discretion and maintains confidentiality
  • Communicates professionally by speaking in terms the audience understands.
  • Speaks and writes clearly, concisely and Meets deadlines and commitments
  • Able to complete work efficiently and learn new technologies and methodologies quickly
  • Able to lead the analysis, design and implementation of IT security solutions
  • Prior experience conducting vulnerability and risk assessments to identify IT system compromises/risk/vulnerabilities or potential compromises/risk/vulnerabilities and their sources. Provides recommendations for remediation
  • Directs or conducts the review, evaluation, and recommendation of software and hardware products, (e.g., virus scanning and repair, encryption, firewalls, internet filtering and monitoring, intrusion detection).
  • Able to structure and process qualitative or quantitative data and draw conclusions or root causes from it.

Extras:
  • Attention to detail -Does not let important details slip through the cracks or derail a project.
  • Resolve - Demonstrates perseverance and willingness to go the distance to get something done.
  • Proactive - Acts without being instructed on what to do. Brings new and creative ideas to the company.
  • Strategic thinking/visioning. Able to see and communicate the big.
  • Determines opportunities and threats through comprehensive analysis of current and future trends
  • Work ethic.
  • Has a track record of working to task completion no matter the difficulty.
  • Expects personal performance and team performance to be nothing short of their best effort.
  • Teamwork. Reaches out to peers and cooperates with supervisors to establish an overall collaborative working relationship.
  • Lead the analysis of system outages, alerts, and/or reports of abnormal system behavior due to suspected security-related events (e.g. viruses, trojan activity, and intrusions)
  • Participate in the Countywide Computer Emergency Response Team (CCERT), Departmental Computer Emergency Response Team (DCERT), and or Security Engineering Teams (SET)
  • Represent their department in legal matters related to IT systems security.
  • Consults with application and software developers to ensure production applications will meet established IT security policies and standards
]]>
Fri, 23 Feb 2018 00:00:00 PST 0
<![CDATA[SQL Developer]]> Our client is seeking a highly talented Database Developer to join their team.  This individual will primarily work on the design, development, implementation and support of client database applications.  The Database Developer will support business functions through use of internally-developed and third-party software solutions, contribute to database and software specifications, and will be responsible for developments and enhancements to computer software programs.  The Database Developer will also perform business analysis, quality assurance testing and database modeling.  This will be a contract-to-hire or direct hire opportunity.

RESPONSIBILITIES
  • Database development, reporting development and data migration
    • Perform database design by analyzing business requirements
    • Develop complex SQL queries, stored procedures, and SSIS packages
  • Define and develop a data migration strategy between different products and platforms
  • Optimization and tuning of SQL
  • Design, develop and migrate SSRS reports
  • Meet with business experts to analyze and document requirements from a database perspective
  • Assist database administrators (DBA) in defining architectural standards for database applications
  • Review applications and database design for compliance with these standards
  • Assist in troubleshooting and resolution of database issues
  • Assist in the application development, debugging, configuration and optimization from a database perspective

 

QUALIFICATIONS

Minimum Requirements:
  • Must have 7+ year experience in relational database development or administration in a commercial enterprise setting
    • B.S. in Computer Science, Mathematics, or Engineering or equivalent work experience
  • 7+ year experience in database design, development/administration and implementation experience may be substituted for degree
  • Must demonstrate a clear understanding of the logical and physical database design (for both transactional and data warehouse) and data normalization concepts
  • Must have extensive hands-on experience with MS SQL Server 2012 SSIS, MS SQL Server 2012 SSRS and Transact-SQL

Preferred Skills/Previous Experience:
  • Excellent, proven troubleshooting and problem resolution skills
  • Must have a team-based attitude and be skilled at building constructive and effective relationships
  • Experience with software development life cycle a plus
  • Strong technical documentation skills
  • Financial industry experience is a plus
  • Programming experience with Financial industry experience is a plus
]]>
Thu, 22 Feb 2018 00:00:00 PST 0
<![CDATA[Senior Security Analyst]]> Position: Senior Security Analyst

Location: Dublin, CA

Client Industry: Retail

Terms: Full Time OR Contract to Hire

Number of positions: 2

About Us: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

About the role:

As a Senior Security Analyst, you will be responsible for validating security requirements adherence, evaluating security services and technologies, and maintaining information security policies and procedures.

Primary Duties and Responsibilities include but are not limited to: 
  • To maintain up-to-date knowledge of the IT security industry, including awareness of new or revised security solutions, improved security processes and the development of new attacks and threat vectors.
  • Assist in researching and evaluating various methods to secure systems, networks, databases, and business applications in support of the project deliverable, related services and other IT organizations.
  • Performs host security certification to ensure compliance with minimum security baselines.
  • Maintains system, database, or network devices minimum security baselines and automated scripts use for host security certification process.
  • Monitor current and proposed laws, regulations, industry standards, and ethical requirements related to information security and privacy, so that the company is warned in advance and is ready to be fully compliant with these requirements.
  • Develop and execute test cases and procedures for validation of project related security requirements.
  • Assist in the execution of project related penetration testing and source code security review, where applicable.
  • Contributes in identifying resolution to security related problems by using creative thinking and problem solving.

Qualifications:
  • Familiarity with firewalls, VPN, PKI, IPS, wireless, IPT, virtualization security, Oracle and MS SQL preferred.
  • Demonstrated experience in risk evaluation and determining mitigating controls.
  • Demonstrated experience in information security for applications, web architectures, operating systems, databases, and networks.
  • Working knowledge of UNIX and Windows.
  • Ability to articulate security issues in terms of business risk.
  • Ability to analyze and solve complex problems.
  • Ability to work in a group setting and independently.
]]>
Thu, 15 Feb 2018 00:00:00 PST 0
<![CDATA[Account Executive]]> Bayside Solutions is seeking a talented, results driven Account Executive to be a part of our high-growth organization.  This is a unique opportunity to join a growing team of business professionals focused on building a first in class market-leader in technologies staffing and consulting services.

A successful Account Executive will thrive in a fast-paced environment, have a willingness to do attitude and possess an entrepreneurial spirit.  They also must have an amazing ability to build great relationships both internal peers and business partners as well as externally, with candidates and clients. 

The career of an Account Executive at Bayside Solutions is rewarding, challenging, prosperous and holds ample opportunity for professional growth. Bayside Solutions offers many career path options and a chance to develop an array of skills. Having been recognized as one of the Bay Area’ s fastest growing private companies, we' re ready to provide you with a challenging and rewarding career.

We believe our success here at Bayside Solutions is a direct reflection of the quality of talented people we hire and develop. New hire training is conducted on a one-on-one basis and covers: recruiting, career consulting and extensive recruiting skills. At Bayside Solutions we make a strong effort and commitment to provide all the tools necessary to ensure the success of every Account Executive.

 

Our Company Bio:

Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at  www.baysidesolutions.com.

 

Job Benefits:
  • An opportunity to join one of the fastest growing private companies in the area, with many possibilities for promotion and career growth
  • Upon receipt of direct hire status, you will be eligible for benefits including medical, dental and vision care, paid time off and holidays totaling more than 20 days a year
  • A competitive base salary and commission structure based on revenue generated
  • Car allowance
  • Cell phone allowance
  • Mileage reimbursement

Summary of Responsibilities:

This is a business development role that requires a successful business professional to develop and execute on a strategy to generate sales revenue by building a maintaining client relationships, seeking to understand the client’ s business needs and initiatives and selling Bayside Solutions’ wide breadth of service offerings to craft a solution to address the client’ s business needs and demands.  The role’ s responsibilities include, but are not limited to:
  • Engage in new and existing client business development activities.  Activities include, but are not limited to: cold calling, qualifying initial clients, identifying potential decision makers, establishing contact relationships, completing company/department profiles and organizational charts, marketing candidates, scheduling and conducting new and follow-up client visits.
  • Develop and execute on business development strategy for market penetration
  • Ability to engage prospective clients confidently; determine interests and motivators of key decision-makers.
  • Qualify opportunities, create target lists for vertical markets
  • Develop superior customer relationships through client meetings, lunches and other out of office activities.
  • Consistently achieves sales quota
  • Conduct market research and qualify target accounts within the local geography. Keep current on market dynamics and trends within specific markets and regions and forecast client demands.
  • Establish client expectations and effectively communicate to appropriate parties to ensure customer satisfaction
  • Facilitate development of professional service agreements (including negotiation of terms when necessary) between Bayside Solutions and clients.
  • Ability to engage prospective clients confidently; determine interests and motivators of key decision-makers.
  • Demonstrate a strong focus on exceptional service to both clients and candidates.
  • Demonstrate well-developed presentation skills including both verbal and written communication skills.
  • Demonstrate a strong commitment to a team environment.
  • Demonstrate strong problem-solving and negotiation skills.
  • Proficient at handling difficult client negotiations with professionalism and respect.
  • Maintain courteous, professional, and effective working relationships with employees at all levels of the organization.
  • Develop, mentor and train assigned recruiters

Required Qualifications:
  • Bachelor’ s degree or equivalent sales/recruiting experience
  • 3+ years of professional outside sales experience in a staffing agency with focus on either an IT or Scientific
  • MS Office experience, including Word, Excel, and Outlook
  • Must be a self-starter who is highly self-motivated to not only meet goals and expectations but to exceed them
  • Exhibit an entrepreneurial mindset and professional image
  • Exhibit strong drive for results and success; convey a sense of urgency to achieve outcomes and exceed expectations; persist despite obstacles, setbacks and competing influences.
  • Quick learner, flexible and adaptable to the changing demands of the business
  • Must have the ability to thrive under pressure to meet hard deadlines
  • Must have a desire to learn and advance in a fast-paced sales environment and excel in a rewards driven culture based on performance
     

Preferred Qualifications:
  • Ability to build and proactively maintain working relationships with a network of technical professionals
  • Strong organizational and negotiation skills
  • Ability to develop and execute on recruiting strategies
  • Strong interpersonal skills to navigate workflow between the recruiting team, candidates and clients.
]]>
Wed, 14 Feb 2018 00:00:00 PST 0
<![CDATA[Quality Analyst I]]> Bayside Solutions is seeking a Quality Analyst I to be part of our Client’ s team in South San Francisco. This is an opportunity to work with a local Biotechnical company focusing on the discovery, development, manufacturing and commercialization of medicines to treat patients with serious or life-threatening medical conditions.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website atwww.baysidesolutions.com.

Quality Analyst I

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Supporting activities for GMP testing laboratories including reagent preparation, equipment maintenance and verification (balance weight checks, spectrophotometer checks, pH electrode maintenance, temperature monitoring, pipet maintenance).
  • Routine housekeeping of laboratories to ensure adherence to cGMP and safety regulations, and to maintain an efficient work environment.
  • Coordinating the receipt and transport of clinical samples for method validation activities.
  • Provide support for cGMP and GLP release and stability testing of preclinical and clinical therapeutic protein samples. 
  • The primary functions of a QC Analyst I include daily, weekly, and monthly maintenance of PAC-V/T GMP Equipment, supporting both lot release, stability, and validation groups. 
  • The Lab Support responsibilities associated with these functions include equipment maintenance and monitoring, reagent preparation and review, and method validation sample management.  
  • A QC Analyst I is expected to precisely follow written procedures, demonstrate accurate documentation skills, and report deviations in a timely manner through the QC discrepancy process. 
  • Other expectations include participating in staff meetings and assigned projects to meet department goals.

Required Qualifications:
  • B.S. in Chemistry, Biochemistry, or related field.
  • The candidate must have excellent written and verbal communication skills, and have strong collaborative skills. 
  • The candidate should also possess keen organizational skills, and be detail oriented. 
  • The candidate must be able to work effectively as part of a multi-disciplinary team responsible for numerous concurrent projects, delivering quality results within specified timelines. 
  • Experience with pH, spectrophotometry, and other wet chemistry assays is preferred. 
]]>
Fri, 26 Jan 2018 00:00:00 PST 0
<![CDATA[Quality Associate]]> Bayside Solutions is seeking a Quality Associate to be part of our Client’ s team in South San Francisco. This is an opportunity to work with a local Biotechnical company focusing on the discovery, development, manufacturing and commercialization of medicines to treat patients with serious or life-threatening medical conditions.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website atwww.baysidesolutions.com.

Quality Associate

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Follow defined internal procedures and comply with cGMP practices.
    Organize, compile and analyzed QC test results - summarize in written reports.
  • Review results to ensure that protocol requirements were met.
  • Communicate deadlines to other groups.
  • Perform compliance checks on data summaries and reports for accuracy.
  • Assist with management of GMP documents, including compiling data binders, scanning and following archiving processes.

Required Qualifications:
  • B.A. or B.S. degree (preferably in Life Science), experience in the pharmaceutical or biopharmaceutical industry a plus.
  • A positive attitude and willingness to learn new concepts in support of commercial QC.
  • Ability to write clearly and effectively. Strong verbal communication skills.
  • Familiarity with GMP requirements and compliance, particularly good documentation practices.
]]>
Fri, 26 Jan 2018 00:00:00 PST 0
<![CDATA[QA Specialist II]]> Bayside Solutions is seeking a QA Specialist II to be part of our Client’ s team in South San Francisco. This is an opportunity to work with a local Biotechnical company focusing on the discovery, development, manufacturing and commercialization of medicines to treat patients with serious or life-threatening medical conditions.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website atwww.baysidesolutions.com.

QA Specialist II

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Provide on-the-floor day to day Quality support to clinical packaging and warehousing operations.
  • Perform routine Manufacturing Quality Assurance tasks, including labeling printing approval, line clearance, QC sampling, and AQL inspection to support clinical packaging and lot release.
  • Perform final review of manufacturing batch records for Genentech manufactured cell banks and clinical large molecule drug substance, drug product and final drug product.
  • Compile Batch History Records for Product Manager review.
  • Scan documents into our GMP document management system.
  • Review and Interact with interdepartmental contacts on discrepancy assessment, resolution, and quality approval.
  • Provide Quality oversight to internal customers in the Manufacturing organization.
  • Collaborate with departments to ensure that all review activities are executed efficiently and effectively.
  • Make independent decisions around complex issues in alignment with GNE policies.
  • Identify and implement process improvements, as necessary.

Required Qualifications:
  • BS/BA degree in the life sciences plus 5-7 years experience.
  • A minimum of at least 5 years experience in Quality Assurance, Quality Control, Manufacturing, or equivalent experience. 
  • Thorough knowledge of cGMPs (Drugs and Biologics), and regulations applicable to U.S. and international Regulatory agencies.
  • Knowledge of cGMPs or equivalent regulations strongly preferred.
  • Ability to interpret Quality standards for implementation.
  • Ability to independently evaluate situations and propose potential solutions.
  • Ability to interpret Quality standards for implementation.
  • Aility to communicate clearly and professionally both in writing and verbally.
  • Flexibility in problem solving and work hours to meet business objectives.
  • Knowledge of SAP and Trackwise applications and project management skills are highly desirable.
]]>
Fri, 26 Jan 2018 00:00:00 PST 0
<![CDATA[Recruiter]]> Bayside Solutions is seeking a talented, results driven Recruiter to be a part of our high-growth organization.  This is a unique opportunity to join a growing team of business professionals focused on building a first in class market-leader in technologies staffing and consulting services.

A successful Recruiter will thrive in a fast-paced environment, have a willingness to do attitude and possess an entrepreneurial spirit.  They also must have an amazing ability to build great relationships both internal peers and business partners as well as externally, with candidates and clients. 

The career of a Recruiter at Bayside Solutions is rewarding, challenging, prosperous and holds ample opportunity for professional growth. Bayside Solutions offers many career path options and a chance to develop an array of skills. Having been recognized as one of the Bay Area’ s fastest growing private companies, we' re ready to provide you with a challenging and rewarding career.

We believe our success here at Bayside Solutions is a direct reflection of the quality of talented people we hire and develop. New hire training is conducted on a one-on-one basis and covers: recruiting, career consulting and extensive recruiting skills. At Bayside Solutions we make a strong effort and commitment to provide all the tools necessary to ensure the success of every Recruiter.
 

Our Company Bio:

Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

 

Job Benefits:
  • An opportunity to join one of the fastest growing private companies in the area, with many possibilities for promotion and career growth
  • Upon receipt of direct hire status, you will be eligible for benefits including medical, dental and vision care, paid time off and holidays totaling more than 20 days a year
  • A competitive base salary and commission structure based on revenue generated
  • On the job training with an impressive success rate (more than 50% of our recruiters had no previous industry experience)


 

Summary of Responsibilities:

This position entails identifying excellent candidates to fill job requirements requested by our clients.

You will develop recruiting skills, including but limited to: generating a high call volume to produce a quantity of potential candidates, quickly and thoroughly screening candidates to learn about the person behind the resume, and maintaining relationships with hundreds of potential candidates. You will need to have excellent communication skills, must be able to build strong relationships quickly and demonstrate a drive to succeed.
  • Source and qualify resumes of industry professionals to identify potential candidates
  • Conduct in-depth phone interviews to recruit potential candidates in various markets that fit the needs and demands of our clients, both technically and culturally
  • Conduct in-person screens and interviews of potential candidates
  • Seek to understand the candidate’ s business drivers and motivations for exploring new opportunities.
  • Prospecting and negotiating contracts with candidates to use our placement services and building a supply of potential contractors
  • Consulting candidates throughout the entire interview process
  • Build and maintain on-going relationships with qualified potential candidates in various different markets.

Required Qualifications:
  • Bachelor’ s degree or equivalent experience
  • 1+ years of professional experience with a focus on customer service in a team oriented environment
  • MS Office experience, including Word, Excel, and Outlook
  • Highly self-motivated to not only meet goals and expectations but to exceed them
  • Quick learner, flexible and adaptable to the changing demands of the business
  • Must have the ability to thrive under pressure to meet hard deadlines
  • Must demonstrate the ability to work in a fast-paced, team-centric environment
  • Exceptional ability to multi-task and possess prioritization skills
  • Excellent verbal and written communications

?Preferred Qualifications:
  • Ability to build and proactively maintain working relationships with a network of technical professionals
  • Strong organizational and negotiation skills
  • Ability to develop and execute on recruiting strategies
  • Strong interpersonal skills to navigate workflow between the recruiting team, candidates and clients.
]]>
Tue, 23 Jan 2018 00:00:00 PST 0
<![CDATA[Research Associate I/II]]> Bayside Solutions is seeking a Research Associate I/II to be a part of our partner’ s team in the Mountain View area. He/She will be responsible for the execution of established protocols and methods and will interface directly with the fermentation and analytical groups. Our partner’ s culture is fast paced and passionate about manufacturing proteins.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Research Associate I/II

Job Benefits:
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Perform recovery, chromatography, and in-process analytics at various process stages and scales.
  • Analyze and communicate results in a timely and effective manner.
  • Maintain organized, neat records and summarize data.
  • Collaborate with cross-functional teams.

Required Qualifications:
  • B.S. in Biochemistry, Biology, Chemistry, or relevant scientific discipline with at least 1 year of lab or industry experience.
  • Strong written and verbal communication skills required.
  • Physical ability to lift up to 40 lbs. and work at the lab bench for an extended duration.
  • The position requires the ability to walk and/or stand for an extended duration.
  • Experience with centrifugation, FPLC/HPLC, column packing, SDS-PAGE, UV-Vis desirable.
]]>
Tue, 23 Jan 2018 00:00:00 PST 0
<![CDATA[Reagent Manufacturing Technician II]]> Bayside Solutions is seeking a Reagent Manufacturing Technician II to be part of our client’ s team in the South  Bay. This is an opportunity to work with the largest biotech company and deliver better-targeted therapies.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of America’ s best companies to work for by Forbes.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Reagent Manufacturing Technician II

The Reagent Manufacturing Technician II will be an integral part of a team that produces reagents used to carry out the Harmony (NIPT) test. This person will be directly responsible for reagent filling and packaging activities. The ideal candidate would have direct experience with equipment set-up, filling activities, and final kit packaging in a GMP environment.

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary  of Responsibilities:  
  • Coordinates and executes reagent manufacturing.
  • Maintains records and clean room environment to comply with good manufacturing practices and standard operating procedures.
  • Maintains production and laboratory equipment and environment.
  • Dispense and aliquot chemicals and reagents from bulk containers.
  • Setting up and operating automated filling equipment.
  • Print and apply container labels.
  • Perform final kit packaging.
  • Ensures sufficient inventory levels of consumables and provides recommended purchases to management to keep stock at sufficient levels.
  • Assists in the development of reagent manufacturing SOPs and documentation.
  • Assists with setting up and establishing protocols for using new equipment introduced to the lab.
  • Assists in process and product verification tests for reliability, robustness, and stability.
  • Supports continuous improvement in both processes and materials.

Required Qualifications:
  • 3 or more years related hands-on experience in a reagent manufacturing GMP environment.
  • Strong technical skills.
  • Experience with manual and automated dispensing/filling equipment.
  • Demonstrated problem solving skills.
  • Demonstrated ability to work effectively in a team environment.
  • Proven math skills.
  • Experience with Excel.
  • Strong written and verbal communication skills.
  • Proven ability to meet deadlines and work under aggressive timelines.
  • High School Diploma or GED required.

 
]]>
Thu, 18 Jan 2018 00:00:00 PST 0
<![CDATA[IT Manager 1: Host Security (PM)]]> IT Manager (Host Security)

Industry: Retail

Location: Dublin, CA

Job Duration: Direct Hire / FTE

 

Join Us

Bayside Solutions is an industry-leading provider of staff augmentation and consulting services. Since 2001, we' ve built our company around a single concept - relationships. We focus on the people we serve. We' re straightforward, consistent and 100% accountable. We deliver intelligent solutions that help our clients and candidates thrive.

 

The Role

Our client is looking for a Talented IT Manager (Host Security) that will be responsible for evaluation, selection and implementation of solutions to address current and future business needs. Highly visible role with IT executives and directly interface with the business community.

 

Deliverables
  • Serve as project delivery issue escalation and communication point for security delivery challenges.
  • Manage project delivery resources of security architects, engineers, analysts, and operators, and prioritize project and operational work efforts.
  • Coordinate project delivery efforts with other teams such as security operations, network operations/architecture, governance & risk, technology engineering.
  • Communicate project and operational metrics.
  • Ensure that new designs meet those standards.
  • Interprets information security and compliance requirements and develops plans to align company security infrastructure to those requirements
  • Assist with management of a multi-million dollar budget (capital and expense).
  • Maintain relationships with 3rd party vendors
  • Coordinate strategic and tactical plans, projects, service transition and contracts.

 

You Have
  • Bachelor' s degree in information systems, computer science, or a related technical discipline
  • 5+ years of IT experience
  • 3+ years in supervisory position of security related staff/projects
  • Prior experience and proven success in managing staff remotely, across multiple time zones
  • Demonstrated ability to anticipate and handle critical situation, negotiating solutions, resolving conflicts, and driving projects to completion
  • Demonstrated ability to execute ROI (basic financial analysis)
  • Techno-functional and has the ability to supervise engineers, analysts, consultants and external vendor resources.
  • Outstanding verbal and written communication skills; outstanding listening skills
  • Able to articulate issues, build consensus around recommendations, and define next steps
  • Highly organized and detail oriented

 

Competitive Advantage
  • Solid understanding and knowledge of End-point/Host security concepts, processes and general trends in the industry
  • Experience with delivery of specific technologies to secure endpoint systems i.e., anti-malware, advanced threat detection, security incident & event management(SIEM), behavior analytics, mobile device management(MDM) security
  • Solid knowledge of IT Infrastructure designs, technologies, products, and services which include knowledge of networking protocols, operating systems, databases, encryption, and other technologies.

 

 


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Wed, 17 Jan 2018 00:00:00 PST 0
<![CDATA[IT Manager II: Technology Solution Architecture]]> IT Manager II (Technology Solution Architecture)

Company: Retail

Location: Dublin, CA

Principal Duties and Responsibilities include but are not limited to: 
  • Ensure accuracy of financial deliverers such as Bill of Materials, quotes, SOW’ s and adherence of architecture deliverables to Company' s standards and project requirements.
  • Partner with peers to gain alignment on new technology standards, understand technology impacts to upcoming projects and changes in strategies for their relevant areas.
  • Participate in the development of the technology roadmap that aligns with the strategic objectives of particular business units and the various technology groups.
  • Support the architecture deliverables and milestones for projects as part of the systems development lifecycle.
  • Manage, mentor and coach a team of technology solution architects that cover various technology disciplines such as networking, storage, systems or other infrastructure technologies.

Qualifications:
  • At least 5 years of experience managing a team of solution or enterprise architects.
  • Experience with Citrix VDI platforms and technologies
  • Experience with major Operation System platforms including Windows server and desktop technologies, UNIX/Linux/Solaris, and virtualization platforms such as VMWare
  • Experience with large enterprise networking technologies and concepts including routing, switching, firewalls, load balancing
  • Strong background in infrastructure technologies
  • Experience with Enterprise storage and backup platforms and technologies
  • Experience sizing infrastructure components to meet various application requirements including high availability considerations, disaster recovery needs, security requirements and operational requirements




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Mon, 15 Jan 2018 00:00:00 PST 0
<![CDATA[Clinical Program Leader]]> Bayside Solutions is seeking a Clinical Program Leader to be part of our Client’ s team in South San Francisco. This is an opportunity to work with a local Biotechnical company focusing on the discovery, development, manufacturing and commercialization of medicines to treat patients with serious or life-threatening medical conditions.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Clinical Program Leader

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Through appropriate leadership, direction and operational expertise, lead the development and execution of operational strategies for multiple molecules/programs in early development portfolio.
  • Represent Clinical Operations on the Early Development Teams (i.e. Core, Development or Clinical Sub-Teams).
  • Develop program timelines and budgets and manage variance.
  • Provide strategic, operational input to clinical development plan (CDP), target product profiles (TPP) and project plans.
  • Lead the Clinical Operations team to ensure effective development, implementation and execution of all clinical trials within agreed timelines, resources and budget.
  • Develop and present operational plan to management review bodies.
  • Identify program risks and develop and implement mitigation strategies for assigned programs.
  • Define the resourcing and outsourcing strategy for early development programs.
  • May participate in Business Development assessments.
  • Work collaboratively, effectively, and efficiently with all internal and external partners and stakeholders.
  • Partner with Business Management to identify strategic business needs to support the clinical programs.
  • Partner with late-stage development leaders to ensure strategic alignment on the CDP Functional Management.
     
Required Qualifications:
  • Bachelor’ s Degree or equivalent required (scientific or healthcare discipline preferred) Advanced degree preferred.
  • 10+ years’ experience of clinical and drug development, including 5+ years of clinical trial management experience and 2+ years of clinical program management experience.
  • Working knowledge of international regulatory and ICH GCP guidelines.
  • Demonstrated understanding, knowledge, and experience of drug development in a complex setting with particular focus on early development.
  • Demonstrated experience in various therapeutic areas.
  • Strong analytical and strategic agility skills.
  • Exceptional leadership skills, including motivation and delegation.
  • Strong financial acumen with experience managing clinical program budgets.
  • Proven ability to implement and manage a clinical program (i.e. a series compromising a clinical development plan).
  • Ability to drive, encourage and support innovation.
  • Highly effective verbal and written communication skills in English.
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Wed, 10 Jan 2018 00:00:00 PST 0
<![CDATA[Project Manager III]]> Bayside Solutions is seeking a Project Manager III to be part of our client’ s team in South San Francisco. Imagine yourself collaborating with an organization focusing on the discovery, development, manufacturing, and commercialization of medicines to treat patients with severe or life-threatening medical conditions.

Our Company Bio:  Founded in 2001, Bayside Solutions is one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four-plus years and over 95% repeat business.

Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success!

You can find additional information on our company website at www.baysidesolutions.com.

Project Manager III

Summary of Responsibilities
  • Managing CMC teams for pipeline products from Toxicology production through Phase I/II/III process development and clinical manufacturing.
  • Work closely with the Technical Development Leader (TDL) to manage the team including timeline, resources, escalating issues, following up on action items and meeting preparation and follow up (agendas, meeting minutes, etc).
  • May be required to assist with creating presentations including timelines, strategy, budget and resources for governance committees and other reviews. 
  • This position requires excellent communication, collaboration, influencing, planning and strategic thinking.
  • Applies project management expertise including planning, tracking and performance management
  • Facilitating technical development team meetings and documenting decisions, risks and actions.
  • Provide timely information for reporting such as the annual budgeting process, governance committees, Monthly Project Reporting, Milestone/schedule tracking etc.
  • Must be able to independently manage priorities and assignments across multiple projects simultaneously.
  • Act as catalyst and primary contact for multiple functional areas across project teams, ensuring good cross-functional collaboration and healthy team dynamics to drive project work forward.

Required Qualifications
  • Undergraduate degree in science, engineering and/or business (MBA) or commensurate experience. PMP certification a plus.
  • For the position, an absolute must is experience in pharmaceutical development. This means someone who has actively worked (3+ years) on supporting or project management for CMC development of new drugs or line extensions (e.g, approval of new indications) for approved drugs.
  • 3 years+ experience of relevant work in project management within biotech or the pharmaceutical industry
  • Strong knowledge of CMC drug development, manufacturing processes and relevant regulations (e.g., cGMP).  
  • Proficient in MS Project and MS Office applications.  Planisware experience a plus.
  • Must work well in a collaborative team environment and communicate effectively with all levels of the organization
  • Excellent written and verbal communication skills.
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Wed, 10 Jan 2018 00:00:00 PST 0
<![CDATA[.NET Developer]]> Our client is seeking a highly talented Senior Application Developer to join their team to help provide internally-developed and third-party software solutions to meet business needs.  This individual will manage technical aspects of assigned projects, including planning and resolving issues.  The Senior Application Developer will also work independently to convert business requirements to Technical Design Specifications, and design/develop code for enterprise-wide and other projects.  This will be a contract-to-hire or direct hire opportunity.

RESPONSIBILITIES
  • Develop software, primarily in C# and ASP .Net
  • Provide expertise in the use of the Microsoft .Net stack, including best practices and design patterns.
  • Significantly contribute to software design and architecture
  • Develop both new applications and improve our existing ones in performance, capability, and reliability
  • Responsible for managing technical development of software from inception through user acceptance, including projects which affect multiple departments and/or pose high risk situations
    • Designs steps and modules, defines timelines, identifies and resolves issues. 
    • May assign work and provide oversight to others
    • May serve as technical lead and make decisions regarding technical direction
  • Presents options and manages client expectations
  • Utilizes design skills to define Technical Design Specifications for complex and high impact projects
  • Creates logic flow charts and process diagrams
  • Creates and/or modifies code to meet specifications
  • Tests and debugs work
  • Supports production software operations during normal business and off-hours
  • Troubleshoots and resolves client issues (May be responsible for client support to an entire business unit)
  • Researches external software solutions

 

QUALIFICATIONS

 

Minimum Requirements:
  • 5-7 yrs. experience in developing software programs; or equivalent combination of education/experience
    • Deep understanding of the C# language and ASP.Net
    • Solid understanding of Enterprise Applications Development and strong design skills
    • Previous experience serving as a team and/or technical lead in software applications development projects preferred
  • Languages/Skills:  C#, ASP.Net, T-SQL, jQuery, JavaScript, HTML5, AJAX, REST, SOA
  • Deep understanding of Web API’ s and micro-service patterns
  • Expert in the Microsoft .Net Runtime through version 4.5, including WCF, LINQ, TPL, and other modern libraries
  • Expert in best practices and design patterns in Microsoft .Net
  • Bachelor’ s degree in MIS, Computer Science, Engineering, Physics, Mathematics, or related discipline
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Tue, 09 Jan 2018 00:00:00 PST 0
<![CDATA[Scientist I]]> Bayside Solutions is seeking a Scientist I to be part of our client’ s team in the East Bay. This is an opportunity to work with the largest biotech company and deliver better-targeted therapies

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of America’ s best companies to work for by Forbes.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Scientist I

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary  of Responsibilities:
  • Organize, conduct and monitor laboratory experiments utilizing established and published procedures, and technical and theoretical understanding.
  • Assumes responsibility for the accuracy, quality, and timeliness of experimental results.
  • Summarizes experimental results, and reviews conclusions with supervisor/project leader.
  • Communicates results of experiments.
  • Keeps supervisor/project leader informed of project status, particularly of significant findings and results in critical problem areas.
  • Performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g., OSHA). 
  • Analyzes and interprets experimental data using various data analysis software and/or applying quantitative methods.
  • Uses technical writing skills to produce reports and documents.
  • May present findings at internal meetings. 
  • Assumes accountability for electronic lab notebook documentation, ensuring experimental methods and results are recorded timely, accurately and consistently, and according to established formats. 
  • Participates in routine lab maintenance, lab safety, ISO, and QSR implementation.      
  • May troubleshoot issues related to instrumentation. 
  • Works independently and manages own work flow to accomplish assigned objectives.   
  • With guidance, analyzes and brainstorms alternative approaches to solve problems and finds solutions.
  • Makes sound recommendations to solve problems.
  • Establishes as appropriate internal/cross-functional/customer relationships. 
  • Uses discretion and independent judgment to recommend solutions to basic problems that their individual or team projects.

Required Qualifications:
  • Bachelor’ s degree in Biological/Life Sciences, Chemistry, Biochemistry or related field, or equivalent combination of education and work-experience.
  • 0-3 years of relevant industry experience.
  • Ability to execute relevant laboratory experimentation.  
  • Ability to recognize and resolve basic problems encountered in experimental procedure. 
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Mon, 08 Jan 2018 00:00:00 PST 0
<![CDATA[Sitecore Developer]]> Sitecore Developer

Banking

Location: San Francisco, CA

Principal Duties and Responsibilities include but are not limited to:
  • Responsible for hand-on development and 3rd party vendor system integration support.
  • Design robust integration between Sitecore as CMS to web analytics and email marketing platform.
  • Partner closely with technical teams supporting infrastructure builds, application development and testing.
  • Works as part of the digital implementation team to meet with business and IS teams to identify problems and define design.
  • Lead end-to-end (conception, development, maintenance and evolution) implementation of digital solutions using Sitecore.
  • Creates artifacts following Bank’ s standards to document the proposed design. These artifacts will be created by eliciting, analyzing, validating and managing technical requirements definition, flows and deliverables for projects.
  • Provides assistance to support teams during troubleshooting and issue triage, helping to resolve issues and identify gaps that would need remediation.
  • Adhering to and complying with all applicable, federal and state laws, regulations and guidance, including those related to Anti-Money Laundering (i.e. Bank Secrecy Act, USA PATRIOT Act, etc.).

Qualifications
  • Familiar with WCAG 2.0 compliance guidelines.
  • Bachelor’ s degree in Computer Science or related degree preferred.
  • Must have 7+ years of development experience with financial services applications using .Net/C#/MVC and formal education with experience in Computer Information systems (or related field).
  • Integration knowledge and practices.
  • Strong and proven technical skills across various internal and external systems, including Sitecore as multi-site CRM and IBM
  • Information Technology architecture and system & data
  • Marketing Cloud as bulk mail provider.
  • Strong sense of prioritization and execution against critical deliverables, coupled with a sense of personal ownership for key projects / issue resolution.
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Mon, 08 Jan 2018 00:00:00 PST 0
<![CDATA[Scientist II]]> Bayside Solutions is seeking a  Scientist II  to be part of our client’ s team in the East Bay. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Scientist II

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Candidate will be part of a small team which develops and qualifies cell based assays for GMP lot release
  • Candidate' s main duties will be to perform cell based bioassays to assess relative potency of large molecule biologics
  • Cultivate mammalian cells, including routine maintenance such as media prep, myco and viral path testing, cell banking
  • Perform real time documentation, and some data management, including data review and control charting
  • Maintain laboratory equipment, restock laboratory supplies, place orders, and submit work orders and other routine tasks as needed
  • Initiate and complete scientific experiments in a team environment
  • Independently execute test methods
  • Present analytical results in a clear manner
  • Perform basic troubleshooting for technical problems
  • Work in an efficient manner and complete assignments in a timely manner

Required Qualifications:
  • Bachelor’ s Degree in biology, chemistry or related science
  • 2-4 years of experience running cell-based assays in the context of relative potency
  • 2-4 years of experience running bioassays such as proliferation, viability, cytotoxicity, activation
  • 2-4 years of experience with readouts such as luciferase, absorbance, fluorescence
  • 1-2 years of experience running ELISAs
  • 2-4 years of experience with mammalian cells
  • Proficiency with analytical software such as SoftMax Pro and PLA
  • Experience with analytical testing, and an understanding of GMP regulations in the context of testing
  • Ability to multi-task and prioritize as needed to meet assigned deadlines
  • Excellent facilitation, organizational and problem solving skills
  • A great attitude and a willingness to work hard with the team
  • Strong interpersonal and communication skills (both written and oral)
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Wed, 03 Jan 2018 00:00:00 PST 0
<![CDATA[Scientist II]]> Bayside Solutions is seeking a Scientist II to be part of our client’ s team in the East Bay. This is an opportunity to work with the largest biotech company and deliver better-targeted therapies

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of America’ s best companies to work for by Forbes.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Scientist II

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary  of Responsibilities:
  • Works under general supervision to conduct and monitor laboratory experiments utilizing established and published procedures, and technical and theoretical understanding.
  • Makes recommendations to resolve problems encountered during experimental procedures.
  • Assumes responsibility for the accuracy, quality, and timeliness of experimental results.
  • Summarizes experimental results, and reviews conclusions with supervisor/project leader.
  • Communicates results of experiments in the form of reports and presentations.
  • Keeps supervisor/project leader informed of project status, particularly of significant findings and results in critical problem areas.
  • Performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g., OSHA).
  • Analyzes experimental data using various data analysis software and/or applying quantitative methods.
  • Forms conclusions, and provides/documents process improvements.
  • Uses technical writing skills to produce reports and documents.
  • May present findings at internal meeting.
  • Assumes accountability for own electronic notebook documentation, ensuring experimental methods and results are recorded timely, accurately and consistently, and according to established formats.
  • Participates in routine lab maintenance, lab safety, ISO, and QSR implementation.
  • May troubleshoot issues related to instrumentation.
  • Keeps informed of trends and developments in area of scientific responsibility.
  • Knows and effectively uses the broad concepts of a particular field or specialization to resolve problems of limited scope and complexity.
  • May act as a lead for assigned projects or team.

Required Qualifications:
  • Bachelor’ s degree in Biological/Life Sciences, Chemistry, Biochemistry or related field, or equivalent combination of education and work experience. Master' s degree preferred.
  • Typically 2 to 6 years of relevant industry experience.
  • Ability to design and execute relevant laboratory experimentation and determine next steps within the context of overall project goals and direction.
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Wed, 03 Jan 2018 00:00:00 PST 0
<![CDATA[Scientist I]]> Bayside Solutions is seeking a Scientist I to be part of our client’ s team in the South  Bay. This is an opportunity to work with the largest biotech company and deliver better-targeted therapies.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of America’ s best companies to work for by Forbes.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Scientist I

The Scientist will provide scientific excellence and guidance in sample preparation for the nanopore platform. The candidate will contribute to the optimization and development of sample preparation protocols that enable sequencing-based assays in a wide variety of applications. The candidate must be self-motivated, but also be able to work well in a team and with multiple lab groups.

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary  of Responsibilities:  
  • Assist senior Lab personnel in creating sample preparation assays and material to support development of sequencing system.
  • Hands-on experience with basic molecular biology techniques, including DNA isolation and purification, PCR, Biosafety I/II procedures, RNA techniques, and creation of buffer solutions.
  • Experience with Bioanalyzer instruments a strong plus. 

Required Qualifications:
  • Bachelor’ s degree in Chemistry, Biochemistry, Molecular Biology, Microbiology, or other related disciplines is required.
  • Minimal 1 year of experience as laboratory assistant preferred.
  • Must be able to immediately work independently and meticulously as directed  for common workflows such as PCR, qPCR, DNA-bead purifications, and acrylamide gels.
  • The candidate will also be required to quickly learn new techniques in molecular biology and instrumentation as needed by the job. 
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Mon, 18 Dec 2017 00:00:00 PST 0
<![CDATA[Clinical Trial Line Manager]]> Bayside Solutions is seeking a Clinical Trial Line Manager  to be part of our Client’ s team in the South Bay. This is an opportunity to work with a local organization focused on the movement of new drugs or devices from conception to FDA approval.   


The Clinical Trial Line Manager  will be a crucial  to ensuring the success of the Clinical project teams. Someone who has managed a team of CTAs or CRCs with working knowledge of clinical trial documentation, eTMF/TMF, and strong experience with study start-up, maintenance, and close-out would be ideal for this role. Individuals who are passionate about their long-term growth  within an organization and have a proactive mindset would be a great fit for this team.

Our Client’ s culture is founded on core values that keep them committed to being a collaborative, innovative, honest, and adaptable place to work. They have built a family within the workplace, promote employees from within, provide opportunities for professional development, and encourage their employees to be active in their efforts to impact their surrounding communities. This has ultimately created an ideal work environment where you can have a fulfilling and balanced career in clinical research.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Clinical Trial Line Manager

Job Benefits:
  • An opportunity to join an organization focused on the movement of new drugs or devices from conception to FDA approval.  
  • Work for a company that is local to the beautiful south bay area.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, vacation/PTO, and 401K.

Summary of Responsibilities:
  • Management of Clinical Research Staff, more specifically Clinical Trial Assistants.
  • Create an environment where Clinical Research staff can successfully achieve established standards of services to clients according to SOPs and contract stipulations.
  • Coordinate with Project Managers and Client Managers in the identification and resourcing of consultants that meet business needs in a cost effective manner.
  • Participate in recruitment of staff; review CVs, conduct telephone and face-to-face interviews and reference checks.
  • Monitor performance of direct reports on a continuous basis, and perform periodic evaluations according to company policies and procedures. This may include solicitation of feedback from clients, client managers, and others, conducting performance discussions, and setting future goals.
  • Identification of and communication to direct reports regarding performance issues, including advising of issue(s), and assessing additional training as needed.
  • Conduct Monitoring Performance Assessments, and other training as needed.
  • Interface with Human Resources regarding compensation, salary adjustments, promotions, disciplinary actions and other related tasks concerning employee evaluations, performance and sub-contractor performance.
  • Work with Human Resources for development of performance plan, as required.
  • Coordinate the training of staff in the areas of company’ s time and expense systems, travel policies and guidelines, overall management structure, professional conduct expectations regarding communication and deliverable expectations.
  • May negotiate consultant sub-contract terms and conditions that meet company standards and practices.
  • Participation in regular meetings regarding project staffing requirements, and other business activities.
  • Maintenance of shared staff assignment spreadsheet.
  • Communication of staff assignment changes and salary updates to HR personnel.
  • Collaborate with Project Managers in establishing project-specific expectations for direct reports allocated to the projects, and assures they are understood by direct reports.
  • Communication of any direct report performance issues to Director of Line Management.
  • Review time and expenses reported by direct reports to ensure utilization of time as well as management of client' s resources are consistent, with expectations.
  • Communicate regularly with Project Managers and Client Account Managers regarding performance of direct reports and assessment of project needs.
  • Forward final signed reviews, contracts, essential employments documents, including documentation of training review, to corporate office for record keeping according to company policies.
  • Ensure notes from phone interviews and reference checks are filed electronically on the server or forwarded to the corporate office for scanning to the server.

Required Qualifications:
  • Four or more years of successful CRA experience.
  • Previous direct supervisory experience preferred.
  • Detail oriented.
  • Excellent organizational skills and strong problem solving skills.
  • Familiarity with medical and pharmaceutical industry, and related terminology and practices.
  • Willingness to travel as needed.
  • Appropriate knowledge of FDA regulations and their practical implementation.
  • Excellent interpersonal, communications, and management skills.

Preferred Qualifications:
  • Ability to work well under pressure, and meet multiple and sometimes competing deadlines.
  • Ability to demonstrate cooperative behavior with colleagues and supervisors.
  • Excellent organizational skills.
  • Flexibility with changing priorities.
  • Critical thinking and problem solving skills. Able to make supported decisions.
  • Excellent communication and listening skills, including influencing and leading, delegation, and team development.
  • Strong negotiation skills, conflict management, and adaptability.
  • Computer proficiency in Microsoft Outlook, Word, Excel, Access, Project, and PowerPoint.
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Fri, 08 Dec 2017 00:00:00 PST 0
<![CDATA[Quality Systems Support Associate]]> Bayside Solutions is seeking a Quality Systems Support Associate  to be part of our Client’ s team in Marin County. This is an opportunity to work with a local Biopharmaceutical company focusing on the developing and commercializing novel therapies for rare diseases.  

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. Their company has been recognized as one of the fastest drug developers in the industry and has also been recognized among the Top 10 World’ s Most Innovative Company’ s in 2015 & 2016.Their organization is fueled by their employee’ s passion and dedication to change the course of disease.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Quality Systems Support Associate

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Review and closure of QC discrepancy reports within specified timelines: EM excursions, laboratory deviations, laboratory investigation reports, out of specification/trend reports.
  • Provide technical expertise and knowledge to QC support group in determining root causes and developing effective CAPAs.
  • Reviewing compendial updates and evaluating current QC practice compliance.
  • Providing departmental metrics.
  • Assisting with the closure of departmental Change Requests.
  • Training record GDP review and resolution. 
  • Assist in the investigation of training discrepancies.
  • Support the FVIII production/project for deviations, discrepancies and training item build for QC.
  • Record entry into Learning Management Systems.
  • Assist with the development and administration of the training system for QC groups.

Required Qualifications:
  • Associates degree or higher with a minimum of 5 years’ experience with GxP environment.
  • Excellent with writing and reviewing skills.
  • Knowledge of discrepancy records (deviations, laboratory investigation reports, out of specification, out of trend) for assignable root cause, development of appropriate CAPAs, and evaluation of CAPA effectiveness a plus.
  • Knowledge of Learning Management Systems and other QC information systems (such as Trackwise, ComplianceWire, document control systems).
  • Experience with compendial updates and compliance.
  • Meticulous record keeping skills, excellent attention to detail.
  • Knowledge of cGMPs and regulations applicable to the FDA and comparable international regulatory agencies a plus.
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Wed, 06 Dec 2017 00:00:00 PST 0
<![CDATA[Mongo DB Developer]]> Position: Mongo DB Developer

Location: San Francisco, CA

Duration: 3 months plus

Responsibilities
  • Analyze data from heterogeneous databases by performing data analysis and implement data migration solution
  • Develop MongoDB, proofs of concept and API prototypes
  • Implement Mongo Management Service for automating a variety of tasks and performance management
  • Implement appropriate indexes (B-Tree, Geospatial, Text) for performance improvement

Qualifications
  • 6+ years of computer science/engineering, IT consulting, and/or IT management experience,
  • Knowledge of modeling/architectural patterns, governance methodologies, and potential limitations within MongoDB
  • Development and designing experience building are usable REST
  • Experience in API model/framework to consume data from and/or push data into MongoDB (or similar technology)
  • Experience working on enterprise applications.
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Wed, 15 Nov 2017 00:00:00 PST 0
<![CDATA[Linux Administrator]]> Position: Linux Systems Administrator

Health care

Location: San Diego CA

Terms: 6 months  contract to hire

SUMMARY

As a Linux Systems Administrator will work closely with  DevOps  to eliminate organizational bottlenecks that hold up deployments that affect our internal and external customers. You must have a passion for continuous learning and be able to conduct R&D to continuously innovate our client’ s infrastructure as well as help other teams with technical issues at the beginning and planning stages of the  SDLC.  This includes (defining) needs/benefits/technical strategy

Linux  Skills:
  • 5+ years of experience in Linux system administration.
  • Support and administration of Linux (Redhat) Cisco,  VMWare,  AWS  and other cloud based technologies
  • Administration and maintenance of networks and computing environments (HW, SW, Systems, Applications and configurations)
  • Installation and configuration of new servers, peripherals, settings, directories, services etc.
  • Rebuilding of existing servers, peripherals, settings, directories, services etc.
  • Develop automation scripts
  • Design new and maintain current server configurations and build documentation
  • Maintain asset configuration documentation and inventory
  • Design, organize, and implement network security measures to protect SW/HW  and Data.
  • Gather data relating to the needs of our customers, and use that info to recognize, forecast, understand, and assess system and network requirements aka capacity planning.
  • Explore new technology, in an effort to implement or recommend its implementation.
  • Daily monitoring of  HW, Server Resource, Systems and processes to verify its integrity and availability.
  • Control dominant consoles in order to oversee the performance of computer systems and networks.
  • Performance of network restart procedures, and maintenance of control records.
  • Performance of security monitoring to identify intrusions
  • Perform daily backups.
  • Perform regular file archival; if necessary, perform purge.
  • Ownership of User accounts: Create, change, and/or delete user accounts.
  • Provide Tier III support to various area’ s - Investigate and troubleshoot issues.
  • Repair and recover from  HW/SW failures.
  • Perform data backups and disaster recovery operations.
  • Update and configuration of system SW which supports infrastructure applications or Asset Management applications.
  • Linux tuning,  HW  upgrades, and resource optimization.
  • Experience working in a 24-7  uptime  environment.

DevOps Skills:
  • Setup and administration of AWS instances (AWS Certified SysOps Administrator or AWS DevOps Engineer preferred)
  • Puppet Configuration Management
  • Setup and administration of Docker containers/Microservices/ Kubernetes
  • Use of Splunk and Nagios

Education: Bachelor’ s degree in Computer Science
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Mon, 13 Nov 2017 00:00:00 PST 0
<![CDATA[Oracle Database Administrator]]> Position: Oracle DBA

Client Industry: Retail

Location: East Bay

Terms: Full Time

Bayside Solutions is seeking a mid-level Oracle DBA to be part of our client’ s growing team in East Bay.

Our Company Bio:  Founded in 2001, Bayside has been recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

About the role:

As an Oracle DBA, you will be involved in the technical design and delivery of database installs, integration, maintenance and upgrade of software to the Oracle platform. You will also ensure database integrity and compliance and monitor database utilization and performance metrics as needed along with providing 3rd  level production support.

Essential Functions:
  • Research, evaluate, develop and implement Oracle Database Engineering designs and standards following industry and best practices.
  • Ensure that current and planned technical solutions are compatible with the company' s business needs and strategic objectives.
  • Work with the other IT organizations to design, develop, and implement Enterprise Oracle Databases in support of development, test, and production environments
  • Provide technical expertise and assistance to other IT and Business groups
     

Qualifications:
  • Bachelor degree preferred, or equivalent combination of education and relevant experience
  • Oracle certification preferred
  • Demonstrated experience with Oracle 11g and 12c, GRID, RAC and DataGuard
  • 5-7 years of experience in system design, implementation and Level 3 support activities
  • Strong technical working knowledge and hands-on experience with server hardware and operating systems
  • Prior experience with DBVault, Encryption, Masking, Subsetting, High Availability, performance management and capacity planning is a plus
  • Experience with Oracle Enterprise Manager (OEM) for monitoring and troubleshooting issues in Development and Production environments
  • Good communication skills are essential.  
  • Must be able to give and receive correct information, explain difficult information in layman’ s terms and maintain a customer service attitude to all levels of users
  • Knowledge of/prior DBA experience with SQL Server and/or MySQL is a plus
  • Ability to work independently, provide leadership, guidance and training to others
  • Ability to provide accurate estimates of time frames and cost estimates necessary to complete potential projects and develop milestones and project implementation plans
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Wed, 08 Nov 2017 00:00:00 PST 0
<![CDATA[Transportation and Logistics Project Manager]]> ROLE:                    Transportation and Logistics Project Manager

LOCATIONS:       South Carolina

INDUSTRY:          Retail

 

Bayside Solutions is seeking a Logistics and Transportation and Logistics Project Manager for our Retail client in South Carolina.  Our client is one of the largest discount retailers in the world and the largest in the United States.  Over the course of 30 years they have grown from a very small clothing retailer with less than 10 stores in California, to a Fortune 500 global giant worth well over $12b annually. 

 

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

 

PRIMARY SKILLS INCLUDE BUT ARE NOT LIMITED TO:
  • Strong Project Management experience in the Transportation and/or Freight Payment IT field.
  • Experience with TMS Systems; preferably Manhattan.
  • Familiar with Carrier Communications to include XML/EDI
  • Experience working on a project team.
  • Strong analytical, problem-solving, and debugging skills
  • Understands data flow diagrams (DFD)
  • Understands and creates swim lane process flows
  • Demonstrated ability to create requirements documentation
  • Demonstrated ability to develop and execute a test plan including leading users through testing
  • Strong written and verbal communication skills
  • Undergraduate degree in Information Systems, or equivalent discipline, or an equivalent business experience

 

NICE TO HAVE:
  • Beginner to Intermediate SQL
  • Grasp of industry best practices within the transportation industry; Domestic and International, Systemic Bid Processes, Freight Payment
  • Experience with the Microsoft Office Suite including Visio
  • Excel and Access
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Mon, 06 Nov 2017 00:00:00 PST 0
<![CDATA[Host Security Engineer]]> Host Security Engineer

Market Segment: Retail

Location: Dublin, CA

Responsibilities
  • In-depth knowledge of Host security products such as File Integrity, End Point Security, End Point Encryption, Mobile Security, Advanced Threat, PKI/Certs.
  • Strong knowledge of current security space with general understanding of current security threats, techniques, and landscape, as well as a dedicated and self-driven desire to research current information on the security landscape.

Qualifications
  • At least 6 years of Information Security experience and at least 4 years with a large organization.
  • Conceptual and practical understanding of IT Infrastructure designs, technologies, products, and services.
  •   Knowledge of Hosting protocols, operating systems, databases, encryption, and other technologies.
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Thu, 26 Oct 2017 00:00:00 PDT 0
<![CDATA[Scientist I]]> Bayside Solutions is seeking a Scientist I  to be part of our client’ s team in the East Bay. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Scientist I

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Help the team with PCR assay development and trouble-shooting.
  • Support optimization and feasibility studies being conducted for an mRNA expression assay.

Required Qualifications:
  • College degree with preferred coursework: biology, chemistry, molecular biology and biochemistry
  • Basic skills: Organized, attention to detail, works well with others and independently, motivated.
  • Some computer experience (especially Microsoft office)
  • Some previous lab work experience preferable
  • Basic knowledge of PCR preferable
  • Some previous work with gene expression preferable.
  • Planning, organizing, executing experiments
  • Learning and applying the fundamentals of PCR
  • Instrument automation for samples and master mixes; Using the Cobas z480
  • Computer analysis of and documenting results in eLN
  • Communication, reports, presentations in weekly meetings and once a year in the department meeting.

 
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Mon, 23 Oct 2017 00:00:00 PDT 0