Medical Device Auditor

About the role

Scarlet is looking for a Medical Device Auditor to join its certification team in Dubai. You will evaluate medical device manufacturers' quality management systems and provide clear, evidence‑based conclusions that support certification decisions. The role combines document review, stakeholder interviews, and limited travel for on‑site audits.

Key responsibilities

• Plan and conduct QMS audits against ISO 13485, EU MDR and UK MDR requirements.
• Review records, interview teams and assess compliance with regulatory standards.
• Document evidence, findings and conclusions in timely audit reports.
• Communicate findings constructively and keep customers informed throughout the audit.
• Review corrective actions and verify evidence needed to close findings.

Required profile

• A degree in a scientific, engineering or medical discipline.
• At least four years of experience in the medical device industry, including two years auditing or managing an ISO 13485 QMS.
• Working knowledge of EU MDR or UK MDR requirements for quality management systems.
• Proven ability to explain audit findings and regulatory requirements clearly, both in writing and verbally.
• Experience with software design, validation, testing and debugging.

Required skills

• ISO 13485
• EU MDR
• UK MDR
• Software design
• Software validation
• Software testing
• Software debugging
• QMS auditing

What we offer

• Competitive salary (£75K‑£90K per year)
• Comprehensive training on Scarlet audit methods and tools
• Limited travel with occasional on‑site visits