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.
- Familiarity with computerized systems and electronic data entry.
- Ability to follow written instructions and adhere to SOPs.
Job Tags
Monday to Friday,