<ul><li>Monitor and implement Quality Management System (QMS) activities within the oral solid dosage production area.</li><li>Review and ensure compliance with SOPs, BMRs, and other GMP documentation.</li><li>Coordinate investigation and documentation of deviations, change controls, and CAPAs.</li><li>Conduct training sessions for production staff on QMS and GMP guidelines.</li><li>Perform periodic review and revision of SOPs in line with regulatory updates.</li><li>Ensure timely closure of quality-related documents like incident reports and risk assessments.</li><li>Support qualification, validation, and calibration activities for production equipment.</li></ul>

Production QMS Officer (Oral)