Quality Assurance Officer

• Directly responsible for quality assurance of the pharmaceutical drug products by enforcing SFDA requirements, Good Manufacturing Practices and other quality related tools in order to meet the quality regulations.

• Review drug product Batch Records and other manufacturing related documents to verify compliance and record keeping for all mandated manufacturing process, quality checks, testing, sampling and sanitization activities.

• Quality Audits related to API, Packaging Components, Labels, and finished products to ensure compliance with established specifications and regulatory standards.

• Follow up with implemented programs (GMPs, Good Hygiene Practices, HACCP, Allergen Control, Cleaning and Sanitization, Pest Control, Equipment Calibration etc.) to ensure compliance by all employees and other personnel involved in the production process in the manufacturing facility.

• Follow up the destruction process with SFDA

• Co-ordinate for the testing results availability involving finished products, raw materials and packaging components and the appropriate release and hold programs associated with these materials.

• Oversee the “On Hold” product program, including the status, release and destruction of Drug Products including its tailings.

• Assist in investigating and correcting quality-related issues (including customer complaints) through proper collaboration with other departments

• Ensure good performance by quality assurance by mentoring, training, setting expectations, providing accountability evaluations.

• Perform other Quality Assurance duties as directed by the Quality Assurance Supervisor .

• Responsible to maintain competence in all responsibility of a Quality Assurance Officer.

Education, Experience and Skills required:

• B.Sc. degree in Pharmacist, chemist, science, industrial Engineering, or chemical engineer.

• 1-3 years of experience in Quality Department.

• communication skill.

• English language.