Medical Device QMS Auditor – ISO 13485 & MDR Focus

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

#J-18808-Ljbffr…