EU MDR Quality Engineer

EU MDR Quality Engineer

The EU MDR Quality Engineer is responsible for ensuring importer and distributor obligations for EU Medical Device Regulation (MDR) verification are fulfilled all over Europe and Turkey, by performing and/or supervising EU MDR verification activities and/or inspectors while content owning EU MDR verification procedures. The role properly escalates issues found during EU MDR verification, monitoring their follow up, and continuously improves the EU MDR verification process in Philips. The EU MDR Quality Engineer is also responsible for performing and supervising inspection of incoming medical devices in Spain, according to local Spanish legislation.

You will be part of the Patient Safety & Quality team in Europe and will be reporting to the Head of Quality Operations Europe.

You are the right fit if;

• Master's degree in quality management, Supply Chain Management, Engineerin...