Regulatory Affairs Specialist – Medical Devices

Il y a 6 heures

belgium belgium Terumo Europe NV Temps plein
pTerumo 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. /ppResponsibilities include preparing and maintaining registration files, reviewing labelling and promotional material for compliance, and monitoring European regulations to support the business across EMEA. /p