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: Solid 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

Perks:
Health insurance
Paid time off
Provident Fund

Work Location: In person

📌 Ipqa Officer Baddi (India)
🏢 Eurocrit Labs International
📍 India