Conformity Analyst (Regulatory) – Medical Devices & Supplements

SGSVerified source: this listing comes from the employer's official hiring system or a verified company · Dubai, United Arab Emirates · Onsite
Listed via SmartRecruiters
Posted Jun 26, 2026 · Apply by Sep 30
Recently checked

Last checked active on Jul 2, 2026.

Position Overview

Compensation: Not disclosed
Position: Entry
Type: Job
Employment: Full time
Practice Area: Regulatory Compliance
Remote: No
Deadline: Sep 30, 2026

Job Description

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

 

 

Practice Area

Position

Entry

Education Requirements

Bachelor degree

Experience Requirements

1 to 2 years

Required Skills

Regulatory Affairs, Stakeholder Management

Industry

Legal

Application Deadline

September 30, 2026

Employment Type

Full time

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