EU MDR Quality Engineer

The EU MDR Quality Engineer ensures importer and distributor obligations under the EU Medical Device Regulation (MDR) are met across Europe and Turkey, owning verification procedures and supervising verification activities and inspectors. The role escalates and monitors issues found during EU MDR verification, drives continuous improvement of the verification process, and performs or supervises incoming medical device inspections in Spain per local legislation. The position is part of the Patient Safety & Quality team and reports to the Head of Quality Operations Europe.