Barrington James is seeking a Medical Device Auditor to assess manufacturers’ QMS against ISO 13485, EU MDR and UK MDR standards. The role involves auditing, interviewing teams, and producing well-evidenced reports. Training is provided, with limited travel to customer sites.
Ideal candidates hold a degree in a relevant field and have at least four years in the medical device sector, including two+ years in auditing or ISO 13485 QMS management, plus knowledge of EU/UK MDR requirements.
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Medical Device QMS Auditor (ISO 13485, MDR) employer: Barrington James
Barrington James is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals in Epidemiology and Real-World Evidence. With a strong emphasis on employee growth, we offer tailored development opportunities and the chance to lead impactful projects across diverse therapeutic areas in the dynamic UK/Europe market. Join us to be part of a team that values flexibility, creativity, and meaningful contributions to healthcare advancements.
