Director, Regulatory Affairs Medical Devices & Combination Product
Takeda Pharmaceuticals • Dublin, Ireland
Role Description
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice (https://jobs.takeda.com/privacynotice) and Terms of Use (https://www.takeda.com/terms-and-conditions/) . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**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...
**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...