Quality Control Analyst
Job in
Novato, Marin County, California, 94949, USA
Listed on 2026-02-20
Listing for:
Tucker Parker Smith Group (TPS Group)
Contract
position Listed on 2026-02-20
Job specializations:
-
Quality Assurance - QA/QC
-
Healthcare
Job Description & How to Apply Below
Duration: 1-year contract with potential to extend or convert
Schedule: Onsite, Monday through Friday
About the RoleThe QC Analytical Analyst is responsible for the timely execution of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products in accordance with cGMP guidelines. This role operates with minimal supervision and requires strong technical expertise, sound judgment, and the ability to recognize and address deviations from established procedures.
Key Responsibilities- Perform biochemical, physical, and chemical analyses of test samples under cGMP guidelines to meet established timelines
- Independently execute assays once proficiency has been demonstrated
- Maintain and expand proficiency across a broad range of analytical methods
- Develop technical understanding of assays and support troubleshooting and laboratory investigations
- Evaluate analytical data against established specifications and acceptance criteria
- Apply technical knowledge to non-routine situations and complex problems
- Identify key issues, analyze root causes, and make sound technical decisions
- Assist with procedure revisions, method and equipment validation, and method transfers as assigned
- Mentor and train junior analysts and new hires in areas of expertise
- Ensure compliance with departmental policies, company standards, and regulatory expectations
- Promote and maintain a strong safety and quality culture
- 1–2+ years of experience in a cGMP or GLP laboratory environment
- 1–2+ years of hands‑on experience with separation sciences (HPLC, UPLC, CE)
- Bachelor's degree in Chemistry, Biology, Biochemistry, or related scientific field
- Strong documentation skills and attention to detail
- Ability to follow written procedures and work with minimal supervision
- Demonstrated leadership capabilities
- Proficiency with Microsoft Word and Excel
- Strong written and verbal communication skills
- Ability to work effectively both independently and within a team
- 1–2+ years of Quality Control laboratory experience
- Additional experience in analytical method validation or troubleshooting
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