Job Description

Review and approve product batch records. Coordinate with the Quality Assurance Manager regarding approval of the Quality Assurance Standard Operating Procedures and all site documents. Assist the Quality Assurance Manager in approving audit plans and audit activities for suppliers and distributors to ensure compliance with Company quality standards. Participate in planned GMP inspection for technical departments to ensure quality policy compliance. Coordinate with the inspector of the Ministry of Health regarding the withdrawal of the production area allocated to the Ministry of Health and any other relevant documents. Responsible for establishing the system required to comply with cGMP and international regulatory authorities and/or standards including the formats they follow..

Requirements:

12 - 15 years of experience in the pharmaceutical industry. Bachelor of Pharmacy or Science "Excellent leadership Good Analytical skills Excellent Analytical Skills. Advanced mathematical skills. TeamWork Result Oriented Problem Solving. Excellent Communicator. Commitment to Safety Fluent English. Excellent Computer skills"