Sr. Executive - IPQA

• Perform line clearance activities prior to production operations.
  
• Review Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and Batch Filling Records (BFR).
  
• Execute in-process QA checks and verifications during manufacturing and packaging.
  
• Manage control sample collection, storage, and documentation.
  
• Collect in-process, finished product, and customer complaint samples as required.
  
• Compile Annual Product Quality Review (APQR) data and perform trend analysis.
  
• Participate in process validation, hold time studies, and related quality activities.
  
• Coordinate with relevant departments for timely batch release.
  
• Conduct routine GMP checks in production, warehouse, and other relevant departments.
  
• Coordinate and review vendor management documents and compile vendor assessment reports.
  
• Manage document archival as and when required in compliance with applicable procedures.
  
• Issue and control formats, Standard Operating Procedures (SOPs), specifications, and batch records.

Qualifications: B.Pharma/M.Pharma/M.Sc (Chemistry)

Exp.- 5-10yrs