Responsible for ensuring compliance with cGMP, GLP, and regulatory requirements in formulation manufacturing.
Review and approve Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and validation documents.
Handle deviations, change controls, CAPA, and OOS/OOT investigations.
Conduct internal audits and support regulatory and customer audits.
Oversee product quality reviews and ensure continuous quality improvement.
Coordinate with Production, QC, and Regulatory teams for process and documentation compliance.
Qualification:
B.Pharm / M.Pharm / M.Sc
Location:
A S Rao Nagar
Salary:
Depends on current & interview experience
Interested Candidates Contact: 7396423749
Job Types: Full-time, Permanent
Benefits:
Health insurance
Provident Fund
Work Location: In person
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