Tucker Parker Smith Group (TPS Group)
Quality Control Technician
Tucker Parker Smith Group (TPS Group), Novato, California, United States, 94949
QC Analyst I
Location: Novato, CA.
12 Month Assignment - high potential to extend or convert to FTE
Pay Rate: $27/hr.
Schedule: Monday to Friday, 8:00 AM to 5:00 PM
Are you ready to apply Make sure you understand all the responsibilities and tasks associated with this role before proceeding.
We’re looking for a motivated, detail-oriented QC Analyst to bring their expertise to our Quality Control team. In this role, you’ll perform biochemical, physical, and chemical analyses of test samples — all while ensuring compliance with cGMP standards. If you have a passion for precision, a solid foundation in lab techniques, and the confidence to work independently on mastered assays, we want to hear from you!
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.
What We’re Looking For: Education:
B.S./B.A. in Biology, Biochemistry, Chemistry, or related field with 2–3 years of relevant lab experience OR A.S. degree with 4+ years of lab experience. Experience:
At least 1 year in a cGMP or GLP laboratory; prior QC experience strongly preferred. Skills:
Hands-on
HPLC experience is a must ; familiarity with computerized systems and electronic data entry; ability to follow SOPs with precision.
Are you ready to apply Make sure you understand all the responsibilities and tasks associated with this role before proceeding.
We’re looking for a motivated, detail-oriented QC Analyst to bring their expertise to our Quality Control team. In this role, you’ll perform biochemical, physical, and chemical analyses of test samples — all while ensuring compliance with cGMP standards. If you have a passion for precision, a solid foundation in lab techniques, and the confidence to work independently on mastered assays, we want to hear from you!
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.
What We’re Looking For: Education:
B.S./B.A. in Biology, Biochemistry, Chemistry, or related field with 2–3 years of relevant lab experience OR A.S. degree with 4+ years of lab experience. Experience:
At least 1 year in a cGMP or GLP laboratory; prior QC experience strongly preferred. Skills:
Hands-on
HPLC experience is a must ; familiarity with computerized systems and electronic data entry; ability to follow SOPs with precision.