Regulatory Affairs is assuring in a demanding and continuously evolving regulatory environment as well as a changing business environment that the medical devices of Terumo are safe and effective and are made accessible to users and patients in the shortest possible time.

The Complaint & Vigilance department is assuring the post market surveillance for medical devices manufactured and/or sold by Terumo Europe N.V. by an established complaint handling process, by timely performing vigilance reporting and by executing product recalls whenever deemed necessary.

Interested in using your expertise to help our business grow in a compliant way? Check out our current open vacancies!