Experienced Medical Device QMS Auditor — ISO 13485 & MDR

Scarlet, a medical device auditing firm, is seeking a Medical Device Auditor to assess manufacturer quality systems against ISO 13485, EU MDR and UK MDR. You will receive training and contribute to certification decisions by reviewing evidence and interviewing teams.

Travel will be limited; you will document findings in audit reports and explain conclusions clearly. The role requires a degree in a relevant discipline and at least four years in the medical device industry, including two years

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