- Follow-up on the implementation of the quality management system under the current Good Manufacturing Practices (cGMP).
- Be responsible for the documentation system including the final approval and the document re-evaluation process.
- Prepare the annual internal audit program.
- Follow-up the non-conformities and deviations with their corrective and preventive actions (CAPA).
- Prepare the management review meeting agenda along with its minutes of meeting.
- Follow-up on the measurement of objectives and key performance indicators (KPIs) set for all the processes.
- Follow-up on the external and internal complaints.
- Report to the top management about the efficiency of the quality management system.
- Train the personnel on quality and current good manufacturing practices principles.
- Prepare product quality review report.
- Perform quality audits.