- Preparing the requirements of the quality management systems in the factory (GMP requirements and ISO system) in coordination with QA Director.
- Conducting external audits (Supplier audit).
- Preparing a plan for internal auditing of all departments, coordinating internal auditing activities (and taking a part in internal audit) then reviewing the corrective / preventive action requests and following up implementation of the corrections.
- Preparing internal audit report & management representative report.
- Preparing management review agenda, writing meeting minutes and final report.
- Follow up of QMS requirements in all departments (quality objectives – KPIs – customer satisfaction …….etc).
- Issue and Follow up change Control action plan.
- Investigate product OOS, OOT and deviations.
- Investigate customer complaints.
- Follow up CAPA execution and effectiveness.
- Member of risk assessment team.
- Any additional work that is requested by his superiors.
B.Sc. of Pharmacy or science.Not less than 3 years of experience in a similar position.Good understanding of the rules and guidance of ISO, GMP and GDP.Good English language.Good Computer skills.Excellent communication skills.Integrity and professional ethics. Attention to detail