<ul><li>Review and approve batch manufacturing records (BMR) and batch packing records (BPR).</li><li>Ensure compliance with cGMP, regulatory guidelines, and internal SOPs.</li><li>Handle deviations, change controls, and CAPA documentation.</li><li>Conduct in-process checks during manufacturing and packing operations.</li><li>Perform internal audits and assist in external audits and regulatory inspections.</li><li>Monitor and ensure proper documentation practices across departments.</li><li>Review and approve SOPs, protocols, and validation documents.</li><li>Manage training programs for GMP compliance.</li><li>Oversee product quality complaints and recall procedures.</li><li>Support continuous improvement initiatives and risk assessments.</li></ul>

QA Executive (IPQA)