Regulatory Affairs Specialist – Medical Devices
Enregistrez cette offre et organisez votre recherche
Créez un compte gratuit pour enregistrer des offres d'emploi, créer des alertes et revenir à cette liste depuis votre tableau de bord.
En continuant, vous acceptez nos Conditions d’utilisation & Politique de confidentialité.
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.