<ul><li>Review and approve batch manufacturing records (BMR), batch packing records (BPR), and other GMP documents.</li><li>Monitor compliance with cGMP, GLP, and regulatory requirements across departments.</li><li>Conduct in-process checks and ensure adherence to SOPs during manufacturing and packaging.</li><li>Coordinate and support validation activities (process, cleaning, equipment).</li><li>Investigate deviations, CAPA, change controls, and risk assessments.</li><li>Review and maintain quality-related documents like SOPs, protocols, and reports.</li><li>Participate in internal audits, external inspections, and regulatory audits.</li><li>Ensure data integrity, documentation control, and archival of QA records.</li></ul>

Officer/Sr. Officer-QA (Documentation)