Key Responsibilities
Ensure GMP, SOP, and company quality standards are followed.
Perform IPQA activities during manufacturing and packaging.
Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
Handle deviations, CAPA, change control, and documentation.
Monitor line clearance before production and packaging.
Coordinate with Production and QC departments for quality compliance.
Maintain QA records, logbooks, and documentation.
Participate in internal audits and regulatory compliance activities.
Requirements
Qualification: B.Pharm / M.Pharm /BSC/ M.Sc.
Experience: 0–3 years in a pharmaceutical QA department.
Valuable knowledge of GMP, GLP, and pharmaceutical documentation.
Basic knowledge of IPQA, BMR/BPR review, and audit processes.
Pay: From ₹15,000.00 per month
Advantages:
Cell phone reimbursement
Internet reimbursement
Provident Fund