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