Regulatory Affairs Associate – Medical Devices & Pharma

About the role

As a Regulatory Affairs Associate for the Gulf region, you will support the regulatory lifecycle of medical devices and pharmaceutical products. You will work closely with cross‑functional teams to ensure timely rebranding and spin‑off projects while maintaining full compliance with local health‑care regulations.

Key responsibilities

• Manage all regulatory activities related to the Gulf rebranding project and meet associated deadlines.
• Oversee regulatory tasks for the Gulf spin‑off project, ensuring timelines are achieved.
• Coordinate with local stakeholders and design centre teams to define steps, activities, and plans for both projects.
• Secure registrations, import permissions, and shipment clearances for medical devices and pharmaceuticals.
• Provide regulatory intelligence and obtain approvals for product submissions.
• Support business objectives, tender participation, and new product introductions.
• Perform product‑quality activities including vigilance, pharmacovigilance, compliant handling, and recalls.
• Monitor emerging regulatory changes affecting medical devices and pharmaceuticals in the Gulf.

Required profile

• Bachelor’s degree or higher, verified before start.
• 2–5 years of regulatory affairs experience, specifically in the Gulf.
• Excellent project‑management, communication, and organizational skills.
• Fluent in English and Arabic.

Required skills

• Regulatory intelligence
• Regulatory Affairs
• Project Management
• Pharmacovigilance
• Regulatory Compliance
• Quality Vigilance