EU Medical Devices Regulatory Director

Takeda Ireland is seeking a seasoned Regulatory Affairs professional to act as the Person Responsible for Regulatory Compliance (PRRC) for medical devices within the EU Authorised Representative. You will lead regulatory activities, ensure documentation is current, and liaise with Notified Bodies and health authorities across the EEA.

You will provide strategic regulatory guidance to product teams, manage risks, monitor changes in EEA requirements, and drive efficient regulatory processes for