<ul><li>Oversee implementation and compliance of cGMP, GLP, and regulatory standards across departments.</li><li>Review and approve BMRs, BPRs, SOPs, change controls, and validation protocols.</li><li>Lead internal audits and support external inspections by regulatory authorities (e.g., USFDA, MHRA, WHO).</li><li>Investigate deviations, OOS, OOT, and complaints; initiate CAPA and risk assessments.</li><li>Ensure timely issuance, control, and archival of quality documentation.</li><li>Monitor qualification and validation activities for equipment, process, and cleaning.</li><li>Coordinate with QC, production, engineering, and R&amp;D teams for quality initiatives.</li></ul><p>&nbsp;</p>

Assistant Manager/Manager-QA (QMS)