Conformity Analyst (Regulatory) – Medical Devices & Supplements

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SGS is seeking a Conformity Analyst (Regulatory) for Medical Devices and Supplements in Dubai for a full-time onsite role. You will manage end-to-end regulatory submissions across the Middle East, prepare EU MDR aligned dossiers, perform product classification and labeling checks, and coordinate with clients and authorities such as MoHAP and SFDA to secure approvals and renewals. The ideal candidate holds a bachelor’s degree in pharmacy, biomedical engineering, life sciences or a related field, with 2 to 5 years of regulatory affairs experience for medical devices or supplements, plus UAE/GCC registration knowledge and ISO 13485 familiarity. To apply, spotlight tangible submission wins, GCC and EU MDR expertise, and include a focused cover letter explaining your fit and readiness to work onsite in Dubai.

Company Description

SGS is the world’s leading Testing, Inspection and Certification company. We operate a network of over 2,500 laboratories and business facilities across 115 countries, supported by a team of 99,500 dedicated professionals. With over 145 years of service excellence, we combine the precision and accuracy that define Swiss companies to help organizations achieve the highest standards of quality, compliance, and sustainability.

We are looking for a Conformity Analyst (Regulatory) – Medical Devices & Supplements in SGS, UAE. The candidate will prepare, review and manage Medical devices and Supplements regulatory.

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, 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.

Qualifications

• Bachelor’s degree in pharmacy, Biomedical Engineering, Life Sciences, Chemistry, or related field.
• 2–5 years of experience in regulatory affairs, product registration or conformity assessment for medical devices, supplements or related healthcare products.
• Working knowledge of EU MDR technical documentation requirements and UAE / GCC registration pathways, including dossier preparation and submission coordination.
• Adept in ISO 13485 quality management system requirements and their application to medical device regulatory documentation and compliance processes.
• Strong documentation, analytical, and stakeholder management skills.

Additional Information