Review of completed Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), validation protocols, reports, and associated documentation to ensure compliance with GMP requirements.
Issuance, control, and reconciliation of Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), and other controlled formats in accordance with document control procedures.
Review and release of semi-finished products after verification of manufacturing documentation, in-process results, and compliance with established specifications.
Review of electronic data generated during manufacturing and quality-related activities to ensure data integrity and compliance with applicable regulatory requirements.




Performance of all In-Process Quality Assurance (IPQA) activities, including line clearance, in-process verification, sampling, documentation review, process monitoring, and GMP compliance during manufacturing and packaging operations.
Support investigations, change controls, deviations, CAPAs, and other Quality Management System (QMS) activities as applicable.
Ensure compliance with current Positive Manufacturing Practices (cGMP), applicable SOPs, and regulatory requirements while performing all assigned quality assurance activities.

📌 Qms Pune
🏢 Emcure
📍 Pune