Scarlet is seeking a Medical Device Auditor based in London or Sweden to audit medical device manufacturers’ quality management systems against ISO 13485, EU MDR and UK MDR requirements. You’ll review records, interview teams and document evidence to reach clear conclusions supporting certification decisions.
You’ll receive training in Scarlet’s audit methods and tools; travel will be limited. A degree in a relevant field and at least four years’ experience in the medical device industry (two
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Medical Device QMS Auditor - ISO 13485 & MDR Focus 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.
