Project Manager Regulatory Affairs (m/f)

REFERENZNUMMER:

277762/11

IHRE AUFGABEN:

-Manage resources and coordinate activities in regard to medical device registrations
-Communicate with notified bodies and participate as well as support within the framework of audits
-Provide both practical, hands-on skills as well as strategic oversight

IHRE QUALIFIKATIONEN:

-Profound experience in a medical device/regulatory environment concerning American, European and Japanese registrations
-Proven leadership and project management skills in a relevant environment
-Outstanding English and German Skills in both verbal and written form
-Willingness to travel for up to 30% of the time (mostly within Europe)

WEITERE QUALIFIKATIONEN:

Regulatory affairs manager