Vacancy Description
Key Responsibilities
- Prepare, compile and submit product registration dossiers for IVD products to MOHAP and other relevant authorities
- Ensure timely renewal and maintenance of product licenses and regulatory approvals
- Classify medical devices and IVD products according to UAE and international regulatory requirements
- Review product labeling, packaging and promotional materials for regulatory compliance
- Liaise and communicate with MOHAP officers and other health authorities for registration follow‑ups and clarifications
- Maintain regulatory databases, documentation and product registration records
- Monitor and interpret changes in regulatory requirements and ensure company compliance
- Collaborate with internal departments Quality, Operations and Sales to ensure all regulatory documentation supports business needs
- Support importation and post‑market surveillance activities as required
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