Conformity Analyst (Regulatory) – Medical Devices & Supplements

Google Chrome Microsoft Edge Apple Safari Mozilla Firefox Conformity Analyst (Regulatory) – Medical Devices & SupplementsFull-timeCompany DescriptionSGS 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 DescriptionManage 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.QualificationsBachelor’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  By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy applyI'm interestedI'm interestedPrivacy NoticeI'm interestedRefer a friendshare this jobShare to WeChat×Copy the link and open WeChat to share.Copy to clipboardOpen WeChatShare to WeChat×Use Scan QR Code in WeChat and click ··· to share.