Analyst, QC I

Novato, CA | Contract

Post Date: 04/11/2017 Job ID: 11010 Industry: Clinical & Scientific

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


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:
  • Performs, under direct or minimal supervision, mammalian and insect cell culture under cGMP to meet specified timelines. 
  • Works independently to prepare reagents or cell culture medium under minimal supervision.  
  • Receives samples submitted to the lab and puts them on test in a timely fashion.
  • Maintains laboratory supply inventories.
  • Maintains mammalian and insect cell lines.
  • Seeds cells for use in in-Vitro potency and infectious titer methods.
  • Maintains the laboratory in an inspection-ready state.
  • Provides support for routine laboratory functions/chores for the QC laboratory.
  • Participates in product/project coordination.
  • Assists in the revision of written procedures as assigned.
  • Develops familiarity concerning cGMP, 21CFR, USP, EP and ICH regulatory requirements.
  • Interacts with other departments, including but not limited to Manufacturing, Microbiology, Quality Assurance, Analytical Chemistry, Formulation, and Process Development. 



Required Qualifications:

  • At least 6 months experience in mammalian or insect cell culture maintenance.
  • At least 6 months 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, LIMS.
  • Viral/ gene therapy work experience is a plus.
  • Good written, verbal, and communication skills.
  • Good documentation skills.
  • Demonstrates the ability to work independently.

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