Director, Regulatory Affairs Medical Devices & Combination Product

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**Job Description**

**OBJECTIVES:**

+ Acts as thePerson Responsible for Regulatory Compliance (PRRC) RA forTakeda’s medical deviceswithinTakeda´sEUAuthorised Representative organization perEU Medical Device Regulation (MDR)2017/745.

+ The RA PRRC of the EU Authorised Representativeis responsible forensuring that the tasks of the AR are fulfilled in the context of regulatory requirements

+ Manages the liaisons to key regulatory authorities (e.g. notified bodies, competent authorities and others asrequired)in the...

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