Job Description

Revise and approve product batch records. Coordinate with the QA manager the approval of QA SOPs and all site documents. Assist the QA manager in approving audit plans and audit activities for suppliers and distributors to assure compliance with Company quality standards. Participate in GMP Planned inspection for technical departments to assure compliance with the quality policy. Co-ordinate with the MOH inspector on the assigned production area withdrawal to MOH, and any other related documents. Responsible for establishing the system required for compliance with cGMP and international regulatory authorities &/or standards including formats that they follow..

Requirements:

Bachelor of Pharmacy or Science 12 - 15 years of experience in the pharmaceutical industry. "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"