<ul><li>Monitor and ensure compliance with cGMP, GLP, and regulatory guidelines across departments.</li><li>Review batch manufacturing records (BMR), batch packaging records (BPR), and other quality documents.</li><li>Conduct in-process quality checks and line clearance activities during manufacturing and packaging.</li><li>Investigate deviations, change controls, CAPA, and ensure timely closure.</li><li>Coordinate with QC, production, and regulatory teams for documentation and compliance.</li><li>Participate in internal audits, vendor audits, and regulatory inspections.</li><li>Prepare, review, and update SOPs, protocols, and validation documents.</li></ul>

Assistant Manager-QA (Analytical)