Key Responsibilities
Ensure GMP compliance in sterile/parenteral manufacturing operations.
Perform line clearance, in-process checks, and area audits.
Review BMR/BPR, logbooks, and production records for compliance.
Support validation activities (Process, Cleaning, Equipment, Media Fill).
Conduct batch review and coordinate batch release activities.
Participate in self-inspections, regulatory audits, and customer audits.
Education: B.Pharm / M.Pharm / M.Sc
Experience: 5 to 8 years in QA of a sterile/parenteral pharmaceutical facility.