<ul><li>Oversee and ensure implementation of Quality Management Systems (QMS) in compliance with cGMP and regulatory standards.</li><li>Review and approve Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and related QA documents.</li><li>Manage deviations, change controls, OOS/OOT, and CAPA in a timely and effective manner.</li><li>Coordinate and support internal audits, external audits, and regulatory inspections.</li><li>Supervise document control activities including SOPs, protocols, and validation reports.</li><li>Ensure qualification and validation of equipment, utilities, and processes as per plan.</li><li>Conduct GMP training and promote quality awareness among employees.</li></ul>

Asst. Manager-QA