Quality Assurance Specialist

Novato, CA 94949

Posted: 06/22/2020 Employment Type: Contract Industry: Clinical & Scientific Job Number: 17588

Job Description

Bayside Solutions is seeking a Quality Assurance Specialist to be part of our  Client’ s team in Novato. 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 Assurance 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:
  • Perform QA review of production records and other documentation associated with production and release of Biological products per QA SOPs
  • Receive, control, scan and archive of completed manufacturing production records
  • Update QA databases for batch record review status
  • Prepare and compile batch record lot history files for Cell Culture or Formulated bulk drug substance (FBDS) lots.
  • Scribe quality review meetings.
  • General administrative functions for the department.
  • Facilitate the routing of technical reports.

Required Qualifications:
  • Bachelor of Science degree in Biology, Biochemistry, Chemistry or related field
  • 1 year experience working in a regulated industry, preferably pharmaceutical, biotech, diagnostic, laboratory environment or similar industry.
  • Ability to understand technical information and report out as required.


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Allison Glogovac

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