Job Responsibilities:
- In-process checks during manufacturing (Granulation, Compression, Coating, Packing)
- Line clearance before batch start-up
- Monitoring of critical process parameters (CPP) & critical quality attributes (CQA)
- Sampling of in-process materials as per SOP
- Verification of BMR/BPR entries during production
- Ensuring compliance with GMP / WHO / regulatory guidelines
- Handling of deviations, change controls & CAPA implementation
- Online documentation and real-time batch monitoring
- Coordination with Production & QC departments
- Environmental monitoring (if applicable)
- Ensuring data integrity practices are followed
Qualification:
- B.Pharm / M.Pharm / B.Sc / M.Sc (Chemistry or relevant field)
Key Skills:
- Strong knowledge of IPQA activities & GMP guidelines
- Positive documentation practices (GDP)
- Attention to detail & compliance mindset
- Basic knowledge of regulatory audits
- Communication & coordination skills
Contact Details:
Phone: +91-XXXXXXXXXX
Email:
[email protected]
Work Location: In person
📌 IPQA Officer (India)
🏢 Pharmaceuticals
📍 India