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naukri

Conformity Analyst (Regulatory) Medical Devices & Supplements

SGS
Dubai, UAE
Mid
2 weeks ago
Regulatory SubmissionsEU MDRMedical Device RegulationTechnical DocumentationProduct ClassificationLabeling Compliance
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Regulatory SubmissionsEU MDRMedical Device Regulation
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Job Description

  • 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.
  • 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.

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