Regulatory Affairs Specialist – Medical Devices

Il y a 1 heure

belgium be Terumo Europe NV Temps plein

Terumo Europe NV in Leuven, Belgium, seeks a Regulatory Affairs Officer to ensure medical devices meet EU/EMEA regulatory requirements. Reporting to the Regulatory Affairs Director, you will join a close-knit team navigating regulatory landscapes and maintaining product approvals.

Responsibilities include preparing and maintaining registration files, reviewing labelling and promotional material for compliance, and monitoring European regulations to support the business across EMEA.