QC Analyst I

Novato, CA 94949

Posted: 06/05/2019 Employment Type: Contract Industry: Clinical & Scientific Job Number: 15843

Bayside Solutions is seeking a QC Analyst I 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.

QC 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:
  • The Quality Control Analyst’ s main job responsibility is to manage the Quality Control In-Process department documents to ensure their accuracy, quality and integrity. The candidate will organize, maintain, track and archive department documents and records while adhering to the BioMarin' s document lifecycle procedures and in accordance with the records retention schedule. The QC Analyst may be required to develop new processes and improve upon the current system to allow retrieval of data records more effectively. Periodically, the QC analyst may be responsible for training employees on records management procedures and policies, which include documentation, retention, retrieval, destruction and disaster recovery. The candidate may also assist with audits of data record systems and perform administrative tasks as needed.
  • Additional daily duties will include sample receipt and accessioning, laboratory housekeeping and infrastructure maintenance responsibilities, reagent preparation and lab supply management. As well as general support of routine testing analytical method or equipment validation, assay method/procedure development, and/or conducting investigations.
  • If time permits the Quality Control Analyst may be trained to perform select microbiological, biochemical and chemical tests of in-process product, equipment, and manufacturing facilities. All microbiological and analytical tests are performed under cGMP guidelines.
  • Work assignments will vary by degree of complexity. Employee is expected to follow SOPs, make appropriate decisions in daily activities with minimal needs for intervention, and be able to recognize deviations from routine practices. Incumbent must accurately complete tasks on time to achieve lab goals, meanwhile limiting GMP / procedural errors.

Summary of Qualifications:
  • Bachelor of Science in a Biological or Biochemical Science with at least 0-2 years of relevant laboratory experience
  • We are seeking a candidate who is self-directed, has the ability to work independently and is highly-motivated.
  • The QC analyst will often work in a fast-paced and deadline driven environment, so it' s important they can stay focused and carry out their tasks in a timely and accurate manner. They should be detail-oriented, dependable and trustworthy since they come in contact with complex and sensitive documents.
  • The QC analyst should have the ability to prioritize, manage time well, multitask and troubleshoot. Strong interpersonal, communication and customer service skills are also essential because the QC analyst will regularly communicate with internal and external business partners.
  • Must have excellent record keeping, written and verbal skills.
  • Ability to perform most tasks without supervision.
  • Experience in quality control practices, current Good Manufacturing Practices or Good Laboratory Practices is a plus.
  • Able to lift up to 25lbs
  • Computer literacy is required, proficiency with Microsoft Word and Excel is essential.
  • Must have excellent record keeping, written and verbal skills.
  • Must have a quality service attitude and focus, exhibit flexibility and willingness to work additional hours to meet production or laboratory process requirements.

Allison Glogovac

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