Job DescriptionEnsure that all processes in the lab in accordance with cGMP & GLP requirements.Ensure that all equipment in the department are calibrated and validated according to a planned maintenance schedule.Ensuring that all staff under my command are properly trained to perform their tasks and undertake their responsibilities.Setting up and revision of Standard Operating Procedures to ensure that the current practices are in accordance with the written procedures which should reflect the current good laboratory practice.Ensure that the implementation of Health & Safety and other legal requirements.Ensure that all necessary testing is carried out.Approve stability protocols, stability reports and other stability procedures and records.Prepare stability files for new products in apex pipeline and product under Re-registration.Ensure that the appropriate documents which required for registration process in EGYPT and KSA (eCTD) are well done and submitted at appropriate time.Qualifications:Bachelor degree of Pharmaceutical science.10+ years of experience in the same position.Excellent understanding of the rules and guidance of GMP, GLP, Stability of pharmaceutical products and Validation of analytical method.Excellent know-how of validation, documentation, internal auditing and training.Strong Leadership and Managerial skills.Growth Mindset.Excellent organizational skills and attention to detail.Strong analytical and problem-solving skills.Proficient with Microsoft Office.Location Preference:Candidates residing near Al Salheya El Gedida, Al Sharqia Governorate (Az Zagazig, Faqous, or Ismailia) are preferred.