<ul><li>Maintain and update the Quality Management System in compliance with regulatory standards.</li><li>Draft, review, and implement Standard Operating Procedures (SOPs) and quality policies.</li><li>Prepare and review quality-related documents such as batch records, validation protocols, and reports.</li><li>Ensure accurate documentation and control of records as per regulatory requirements.</li><li>Conduct internal audits to assess compliance with GMP (Good Manufacturing Practices) and other regulatory standards.</li><li>Identify non-conformities during audits, suggest corrective actions, and follow up on implementation.</li><li>Review and approve change control requests and deviation reports.</li><li>Investigate deviations, out-of-specifications (OOS), and out-of-trend (OOT) results, and recommend corrective and preventive actions (CAPA).</li></ul>

Sr. Executive/Executive-QA (Validation)