Conformity Analyst (Regulatory) – Medical Devices & Supplements

• Manage end-to-end regulatory submissions across the Middle East (UAE, KSA, GCC), including application preparation, tracking and authority coordination (e.g., MoHAP, SFDA).
• Prepare and review regulatory dossiers and technical documentation aligned with EU MDR and regional authority requirements, ensuring completeness and submission readiness.
• Conduct product classification, labeling/claims compliance checks and gap assessments for market entry across UAE and GCC markets.
• Liaise with clients, internal teams, and regulatory authorities to support approvals, renewals, and query/deficiency responses.
• Monitor regional regulatory updates and maintain submission trackers, documentation, and compliance records.

• Bachelor’s degree in pharmacy, Biomedical Engineering, Life Sciences, Chemistry, or related field.
• 2–5 years of experience in regulatory affairs, product regis...

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