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Senior Regulatory Manager - Dusseldorf, Germany Nr ref.: /JOBS.pl Description: My client, a German Pharmaceutical company, is currently searching for a Senior Regulatory Affairs Manager to join their team based in Dusseldorf, Germany. The successful person will ideally have strong registration, Post Approval and CMC background and be fluent in German and English.Your background:*You have experience with the care / Life Cycle Management of current authorizations.*You have experience in the conduct of variation procedures and renewals.*You are willing to take responsibility as an information officer, and possibly also as a wholesale representative.*Have knowledge of technical and functional requirements pivotal documents (CMC member).*Developing appropriate regulatory strategies is not a foreign word for you.*National, MRP, DCP submissions - creation of applications for authorization and supervision of approval procedures.*You like to communicate with customers, authorities, partners and affiliates at home and abroad.Your profile:*You have a scientific education.*6-years of regulatory experience*You have mastered the standard Microsoft Office applications and have database experience.*You are fluent in English and German, both spoken and written.*Mastering an Eastern European language is an advantage.*They are used to working independently; but also a team player.For further details about this role or other opportunities within Regulatory Affairs please contact Tim Barratt on (0) or email a copy of your CV to Kontakt: Aplikuj teraz Ogłoszenie pochodzi z serwisu Jobs.pl .

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