Medical Device Quality Auditor — ISO 13485 & MDR

Medical Device Quality Auditor — ISO 13485 & MDR

Full-Time No working from home possible
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Scarlet, authorised to assess and certify medical devices, is seeking a Medical Device Auditor. You will audit manufacturers’ quality management systems and produce clear conclusions to support certification decisions, with training in Scarlet’s audit methods and tools. Travel will be limited.

You will review evidence, interview teams, document findings, and explain conclusions clearly to customers. Experience with ISO 13485, EU MDR, or UK MDR is essential.

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Medical Device Quality 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.

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Contact Details:

Scarlet Recruitment Team