<p>Responsibilities</p><ul> <li>Assist the Manager during cGMP, Environmental, and Regulatory audits.</li> <li>Assist the Manager to create and collate product master files (dossiers), drug master files (DMF).</li> <li>Generate and Review of CoCs, CoAs, CoMs, BSE documents, CMR documents, RM Certificate of Analysis, RM Safety Data Sheet, RM technical documents, RM composition breakdown, as may be required for local and international submissions.<