Conformity Analyst (Regulatory) – Medical Devices & Supplements

Responsibilities

• Manage end-to-end regulatory submissions across the Middle East (UAE, KSA, GCC)
• Prepare and review regulatory dossiers and technical documentation aligned with EU MDR
• Conduct product classification, labeling/claims compliance checks, and gap assessments
• Liaise with clients, internal teams, and regulatory authorities to support approvals
• Monitor regional regulatory updates and maintain submission trackers and compliance records

Requirements

• Bachelor’s degree in pharmacy, Biomedical Engineering, Life Sciences, Chemistry, or related field
• 2–5 years of experience in regulatory affairs or product registration for medical devices or supplements
• Working knowledge of EU MDR technical documentation and UAE/GCC registration pathways
• Proficiency in ISO 13485 quality management system requirements
• Strong documentation, analytical, and stakeholder management skills

About the Company

SGS is the world’s leading Testing, Inspection and Certification company, operating a network of over 2,500 laboratories and business facilities across 115 countries.