QUALIFICATIONS AND JOB DESCRIPTION
The ideal candidate should be ready to respond to the following skills and experiences;
- University Degree in Pharmacy, Chemical Engineering, Chemistry or Biology, master or MBA is a plus.
- Minimum 7 years of experience in quality assurance in pharmaceutical industry,
- Fluency in both written and spoken English,
- Must be analytical , creative minded and result oriented,
- Strong interpersonal, negotiation, coordination, communication and coaching skills,
- Proficiency in MS Office programs and ERP.
Job Description
- Responsible to improve the quality assurance system according to updated regulations Pro-actively follow the new regulations and implement them in the company,
- Implement all QA processes and procedures,
- Implement customer complaint system and root-cause problem solving that eliminated major customer complaints since implementation,
- Responsible for the evaluation and solving of deviation problems systematically,
- Review and approve all validation and qualification processes,
- Establish key process indicators (KPI’s) and implement preventive and corrective actions to eliminate the root causes of poor quality and delivery problems, responsible for the continuance of GMP conditions,
- Perform preparation of the master files of the products,
- Responsible for the implementation of Change Management System, plan, determine deadlines, approve the completed and appropriate change control requests,
- Responsible for the approval of the batches for shipment to the local and export customers warehouses,
- Responsible for the approval of certificate of analysis including microbiological tests.