| Job Location | Lebanon |
| Education | Bachelor's degree / higher diploma |
| Salary | Not Mentioned |
| Industry | Pharmaceutical Manufacturing |
| Functional Area | Not Mentioned |
- 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.
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