Senior Quality Control Analyst

Vacaville, CA 95688

Posted: 10/12/2020 Employment Type: Contract Industry: Clinical & Scientific Job Number: 18019

Job Description


Bayside Solutions is seeking a Senior Quality Control Analyst to be part of our client’ s team in 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.

Senior Quality Control 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:
  • Participate in sample collection
  • Perform routine assays/laboratory maintenance functions
  • Identify assay anomalies
  • Initiate/assess discrepancies
  • Anticipate problems and notify supervision
  • Understand theory of assays; use SOPs, TPs, specifications, trends, and expertise to propose solutions to assay issues
  • Identify problems and propose solutions to systems
  • Good understanding of global systems and GMP Compliance requirements/regulations
  • Assist in preparing for internal and external inspections by ensure Laboratory is inspection ready at all times.
  • Meet scheduled performance of 95% on time.
  • Perform other duties as requested by supervision to support Quality activities

Summary of Qualifications:
  • Associate or B.S./B.A. degree.
  • 1-3 years’ experience in a Biotechnical or Pharmaceutical Industry or combination of both education and experience. This is an entry level position.
  • Solid verbal and written communication skills, ability to organize and present information both formally and informally.
  • Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures.
  • Routinely exercises sound judgment, reasoning, and problem solving.
  • Capable of completing assigned responsibilities and keeping manager informed of status.
  • Ability to work under minimum supervision to complete assigned tasks in a timely manner.
  • Capable of completing assigned responsibilities and keeping manager informed of status.
  • Strong verbal and written communication skills, ability to organize and present information both formally and informally.
  • NOTE: Position may involve use of reagents and other chemical compounds, including but not limited to acetonitrile, chlorine, acids and bases, biologic toxins, microorganisms and potent compounds

Meet Your Recruiter

Allison Glogovac

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