<ul><li>Supervise QA activities to ensure compliance with cGMP, GLP, and regulatory standards.</li><li>Review and approve batch manufacturing records, validation protocols, and reports.</li><li>Oversee in-process quality checks and ensure adherence to SOPs.</li><li>Handle deviations, change controls, CAPA, and OOS investigations.</li><li>Coordinate with Production, QC, and Regulatory teams for quality-related matters.</li><li>Conduct internal audits and support external regulatory inspections (USFDA, MHRA, WHO, etc.).</li><li>Ensure timely review of documents such as SOPs, specifications, and quality manuals.</li><li>Monitor training programs for QA staff and production personnel on GMP compliance.</li></ul>

Asst. Manager-QA