GMP QC Specialist, CMC — Quality & Release Expert

A biopharmaceutical company based in Pennsylvania is seeking a GMP QC Specialist to ensure compliance with Good Manufacturing Practices. The ideal candidate will have over 5 years of experience in biopharmaceutical technical operations and specific familiarity with microbiological assays. Responsibilities include developing quality control procedures, conducting batch reviews, and managing documentation. This role offers the opportunity to enhance overall laboratory efficiency and work closely with cross-functional teams. #J-18808-Ljbffr