Job Description

• Preparing the requirements of the quality management systems in the factory (GMP requirements and ISO system).
• Preparing a plan for internal auditing of all departments, coordinating internal auditing activities (and taking part in internal audits), and then reviewing the corrective/preventive action requests and following up on implementation of the corrections.
• Preparing internal audit report & management representative report.
• Preparing the management review agenda, writing meeting minutes and final report.
• Follow up on 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 on CAPA execution and effectiveness.
• Member of risk assessment team.
• Conducting external audits (Supplier audit).

Requirements

• B.Sc. of Pharmacy or Science.
• 2:4 years of experience in a Non-Sterile pharmaceutical field.
• 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.