Scarlet seeks a Medical Device Auditor based in London or Sweden to audit manufacturers’ quality management systems in line with ISO 13485, EU MDR and UK MDR. You will gain training in Scarlet’s audit methods and work with product teams to ensure evidence-based certification decisions.
The role involves reviewing records, interviewing staff, documenting findings and producing clear audit reports. Occasional travel may be required to ensure safe, compliant devices reach patients.
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Medical Device QMS Auditor (ISO 13485 & MDR) employer: Scarlet
Scarlet is an exceptional employer that fosters a collaborative and innovative work culture, where your contributions as a Product Designer will directly impact the future of health technology. With a strong focus on employee growth, you will have access to continuous learning opportunities and the chance to work alongside industry experts in a dynamic environment. Located in a vibrant area, Scarlet offers unique advantages such as flexible working arrangements and a commitment to user-centered design, making it a rewarding place to advance your career.
