Job Description

QC Analyst

Location: Novato, CA.

12 Month Assignment

Pay Rate: $27/hr.

Schedule:Monday to Friday, 8:00 AM to 5:00 PM

On behalf of our client a Biopharma company located in Novato, CA. We are seeking a motivated and detail-oriented QC Analyst to the Quality Control team. This individual will perform biochemical, physical, and chemical analyses of test samples in compliance with cGMP standards. The role requires a strong foundation in laboratory techniques, a commitment to data integrity, and the ability to work independently on mastered assays.

Key Responsibilities:

• Perform analytical testing on samples using established biochemical, physical, and chemical methods under cGMP conditions.
• Independently execute assays in which proficiency has been demonstrated.
• Evaluate test results against defined specifications and document findings accurately.
• Support the maintenance of a compliant, inspection-ready laboratory environment.
• Maintain laboratory supplies and ensure proper glassware cleaning and upkeep of routine lab functions.
• Review and revise standard operating procedures SOPs and other documentation as assigned.
• Collaborate cross-functionally with internal departments to support QC operations.
• Stay informed on and comply with regulatory guidelines, including cGMP, 21 CFR, USP, EP, and ICH standards.

Qualifications:

• B.S./B.A. in Biology, Biochemistry, Chemistry, or related scientific field with 2–3 years of relevant lab experience OR A.S. degree with a minimum of 4 years of relevant laboratory experience
• At least 1 year of experience in a cGMP or GLP laboratory setting; prior QC experience highly desired.
• Experience with HPLC is a plus!
• Familiarity with computerized systems and electronic data entry.
• Ability to follow written instructions and adhere to SOPs.

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