- Line Clearance & Inspection: Conducting, verifying, and documenting line clearance before manufacturing and packaging to prevent cross-contamination.
- Aseptic Area Monitoring: Monitoring environmental conditions (temperature, humidity, pressure differentials) and adherence to aseptic gowning procedures in Grade A/B areas.
- Process Monitoring: Conducting in-process checks during sterile formulation, filling, and sealing (e.g., integrity testing).
- Documentation & Review: Reviewing Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and logbooks online for compliance.
- Quality Management: Supporting investigations into deviations, non-conformances, and implementing CAPA (Corrective and Preventive Actions).
- Sampling: Performing sampling of in-process materials and finished goods for testing.
Required Qualifications & Skills:
- Education: B.Pharm, M.Pharm, or M.Sc. in Microbiology/Biotechnology.
- Experience: 1–5 years in IPQA within a sterile or injectable manufacturing facility.
- Skills: Strong knowledge of cGMP, QMS, aseptic techniques, attention to detail, and documentation accuracy.
Job Types: Full-time, Permanent
Pay: ₹15,000.00 - ₹25,000.00 per month
Benefits:
- Health insurance
- Paid time off
- Provident Fund
Work Location: In person
