About the role
The job holder will manage and execute regulatory compliance activities for raw materials and finished products, including data preparation, documentation, submissions, and follow-up with regulatory authorities (EDA, NFSA, CADC, NORCB).
Acts as primary owner for Raw Materials, COAs, and CRM activities while supporting finished product operations based on workload distribution.
Position will be based in our site in Al Obour City and will report to Site Quality Assurance Manager.
Bachelor’s degree in pharmacy, Science, or a related field1–3 years of relevant experience in regulatory affairs, quality, or pharmaceutical operationsStrong knowledge of regulatory requirements (EDA, NFSA, NRC)Attention to detail and documentation accuracyCross-functional coordination (QC, regulatory, finance)Analytical and organizational skills
Bachelor’s degree in pharmacy, Science, or a related field1–3 years of relevant experience in regulatory affairs, quality, or pharmaceutical operationsStrong knowledge of regulatory requirements (EDA, NFSA, NRC)Attention to detail and documentation accuracyCross-functional coordination (QC, regulatory, finance)Analytical and organizational skills
