Job Description
1. In process check during manufacturing and packing.2. Line clearance for area.3. Verification of raw material and packing material.4. Online entries of raw data in APQR.5. Review of logbooks of production and packing6. Monitoring of basic norms of cGMP.7. To review all in process documents.8. Verification of IPQC instruments.9. Execution of process validation / Equipment qualification.10. GMP compliance on shop floor.11. IPQA allocation , monitoring and accountability.Candidates good communication skillscandidates from Tablet Pharma Industries give preferences .Candidates good Computer skills
Role