On-Site GMP QA Associate: Batch Records & Compliance

A biopharmaceutical company in San Diego is seeking a Manufacturing Quality Assurance Associate to ensure compliance with cGMP standards. In this role, you will collaborate with various teams, review production records, and participate in quality-related activities. Candidates should have a Bachelor's degree in life sciences, 2+ years of relevant experience, and familiarity with FDA regulations. This position offers competitive pay and the opportunity to grow in a supportive team environment. #J-18808-Ljbffr