Tucker Parker Smith Group (TPS Group) | Quality ...

QC Analyst ILocation: Novato, CA.12 month assignment Pay Rate: $28hr.On behalf of our client a pharmaceutical leader specializing in the development of therapeutics for patients dealing with life threatening rare genetic diseases. We are seeking a QC Analyst I to perform biochemical, physical, and chemical analyses of test samples under cGMP conditions, ensuring data integrity and compliance with regulatory requirements. The successful candidate will play a key role in maintaining a high standard of quality control while supporting the laboratory's operational needs.Key Responsibilities:Conduct biochemical, physical, and chemical analyses of test samples following cGMP guidelines, meeting specified timelines.Evaluate test results against established criteria and dependently perform mastered assays and develop expertise in a wide range of test methods.Train other analysts in areas of personal expertise.Maintain laboratory readiness for inspections and ensure supply inventory is adequately managed.Oversee routine laboratory functions such as glassware cleaning to meet operational requirements.Develop and maintain familiarity with regulatory requirements, including cGMP, 21CFR, USP, EP, and ICH guidelines.Collaborate with cross-functional teams to address quality control needs.Revise and update written procedures as needed, adhering to company policies and quality standards.Education and Qualifications:B.S.B.A. in Biology, Biochemistry, Chemistry, or a related scientific field, with 2+ years of relevant laboratory experience.Strong ability to follow written instructions with minimal supervision.1+ years of experience in a cGMPGLP laboratory, with a focus on quality control.Proficiency in computer applications, including Windows, Microsoft Word, and Excel.Strong documentation skills and attention to detail.Ability to work independently and as part of a team.Please submit a copy of your resume in PDF or Word Document to be considered.

Created: 2025-01-01