<ul><li>Review and approve batch manufacturing and packaging records to ensure compliance with GMP and SOPs.</li><li>Manage investigations of deviations, non-conformances, and out-of-specification (OOS) results.</li><li>Coordinate corrective and preventive actions (CAPA) and follow up for effective implementation.</li><li>Support internal and external audits, including regulatory inspections, by preparing documentation and ensuring compliance.</li><li>Review and update quality documents, SOPs, and master batch records as needed.</li><li>Conduct training sessions on GMP, documentation practices, and quality systems for production and QC staff.</li><li>Participate in change control and risk assessment activities.</li></ul>

Officer/Sr. Officer-QA