Badr City, Cairo, EgyptInternshipMedical & Healthcare
Pharmaceutical
About this role
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).
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.
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.
