Medical Device QMS Auditor (ISO 13485 & MDR)

Scarlet seeks a Medical Device Auditor based in London or Sweden to audit manufacturers' quality management systems in line with ISO 13485, EU MDR and UK MDR. You will gain training in Scarlet's audit methods and work with product teams to ensure evidence-based certification decisions.

The role involves reviewing records, interviewing staff, documenting findings and producing clear audit reports. Occasional travel may be required to ensure safe, compliant devices reach patients.