<ul><li>Supervise QC laboratory activities, including testing of raw materials, in-process, and finished products.</li><li>Review and approve analytical reports, protocols, and SOPs as per regulatory requirements.</li><li>Ensure compliance with GMP, GLP, and regulatory guidelines (e.g., WHO, USFDA, MHRA, ISO).</li><li>Coordinate and perform method validation and equipment qualification activities.</li><li>Manage laboratory investigations, OOS (Out of Specification), OOT (Out of Trend), and deviations.</li><li>Support stability studies, including protocol preparation, sample management, and data review.</li><li>Monitor environmental and instrument calibration schedules and ensure their timely execution.</li><li>Participate in internal and external audits; ensure audit readiness and address audit observations.</li><li>Mentor and train QC analysts and technicians on analytical techniques and regulatory practices</li></ul>

Deputy Manager-QC