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Job Description
- 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.
Job Requirements
- 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
