Company Description NAPCO PHARMA is a leading Egyptian pharmaceutical company producing over 350 products across all therapeutic areas. Based in Egypt, NAPCO PHARMA operates a state-of-the-art manufacturing facility that is both GMP and ISO certified. The company is dedicated to providing high-quality pharmaceutical products at competitive prices and exports its products to 15 countries across the Middle East and Africa.
Role Description This is a full-time on-site role for a Methodology & Stability Supervisor located in the 10th of Ramadan. The role involves supervising and managing the execution of stability studies, ensuring compliance with regulatory guidelines, developing and validating analytical methodologies, and performing data analysis to ensure product quality. The Supervisor will interact with cross-functional teams to support quality control, contribute to the development/improvement of processes, and ensure compliance with Good Laboratory Practice (GLP) standards.
Qualifications Experience with stability studies, analytical method validation, and related regulatory guidelines Proficiency in laboratory analysis techniques and quality control methods Strong skills in data analysis, report preparation, and documentation Ability to lead and manage teams effectively with strong problem-solving and decision-making capabilities Familiarity with GMP, GLP, and ISO standards Educational background in Pharmaceutical Science, Chemistry, or related fields Previous experience in the pharmaceutical manufacturing industry is an advantage Proficiency in written and spoken English