Sr. QC Associate

Pay Rate Low: 32 | Pay Rate High: 34 Our client is a global, research-driven pharmaceutical manufacturer focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. The company is looking for a Sr. QC Associate to join the team. This is an amazing opportunity to work on cutting edge treatments and make a difference! Title: Sr. Quality Control Associate (Contract) Location: Alameda County, CA Schedule & Contract Contract Duration: 3 months (Likely to extend) Schedule: Monday-Friday, 8:00 AM-5:00 PM Hours: 40 hours per week Job Duties We are seeking a Quality Control Analyst to support analytical testing activities within a cGMP-regulated biopharmaceutical manufacturing environment. This role is responsible for executing and coordinating analytical testing of bulk drug substance and drug product across multiple analytical platforms, including chromatography, potency/bioassays, microbiology, raw materials, cleaning validation, and packaging testing. The analyst will independently perform and review 3-5 analytical methods, ensure accurate documentation, and support data trending, investigations, and compliance activities. Responsibilities include authoring and maintaining QC documentation (SOPs, test methods, specifications, and reports), identifying process improvements, and ensuring adherence to global regulatory requirements (e.g., FDA, EMA). Qualifications High School Diploma with 6+ years, Associate Degree with 4+ years, or Bachelor's Degree in a science or engineering field with 2+ years of cGMP experience Prior Quality Control experience preferred Strong technical knowledge of analytical testing in biopharmaceutical manufacturing Demonstrated ability to independently execute methods, review data, and ensure compliance. INDBH #LI-MG1

Created: 2026-04-19