- 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
Benefits:
- Cell phone reimbursement
- Internet reimbursement
- Provident Fund