EU Regulatory Lead - Medical Devices & Combinations

Takeda Ireland seeks an experienced Regulatory Affairs professional to act as the PRRC RA for EU medical devices under the MDR framework. You will manage liaisons with Notified Bodies and authorities, ensure up-to-date documentation, and drive regulatory strategy and submissions across the EU and EEA.

The role requires leadership, cross-functional collaboration, and strong communication skills to support launches and lifecycle management of device products in the European market.