- Prepare and submit shipment files to EDA and relevant authorities (MOH, GOEIC, etc.).
- Ensure that all required documents (invoices, certificates, permits) are complete and compliant with Egyptian regulations.
- Ensure the company’s compliance with all regulations set by EDA, MOH, GOEIC, and other relevant authorities.
- Follow up on shipment approvals and address any issues or delays to ensure timely clearance.
- Prepare and submit product registration files with the EDA, including supplier communication and coordination with EDA supervisors.
- Manage the registration of new agency/distributor contracts and issue the agency card.
- Maintain and update supplier documents, ensuring all required certificates and regulatory documents are up to date.
- Manage GS1 product compliance (barcode registration, updates, and tracking).
- Coordinate with internal teams (logistics, finance, and legal) to ensure smooth operations and compliance.
Bachelor's degree in Pharmacy, Science, Business, or a related field.Minimum of 2 years of experience in regulatory affairs, shipment approvals, or medical device registration.Very good command of English (both written and spoken) – required for handling supplier communication and official documentation.Strong understanding of EDA, MOH, and import regulations.Experience working with medical equipment ( class I& II )is preferred.Proficiency in Microsoft Office (Excel, Word, Outlook).Strong organizational and follow-up skills.Ability to handle regulatory paperwork and liaise with government agencies efficiently.