- Prepare, review, and submit regulatory dossiers (CTD, , eCTD) for new product registrations and variations across international markets .
- Maintain up-to-date knowledge of regulatory requirements and changes in targeted countries.
- Liaise with health authorities and regulatory agents to follow up on submissions and respond to queries.
- Collaborate with R&D, Quality Assurance, and QC departments to gather necessary documentation for regulatory submissions
Bachelor's degree in Pharmaceutical Sciences, Science or a related field .Experience (1-3) years of in Regulatory Affairs, preferably with international exposure.Solid knowledge of global regulatory frameworks (WHO, ICH, GCC, SFDA, etc.).Familiarity with CTD/ eCTD formats.Strong communication skills in English (written and verbal); French is a plus.Excellent organizational, time management, and problem-solving skills.Ability to work independently and collaboratively in a cross-functional team.Pharmaceutical Experience is a must .6th October City resident and nearby are preferred .