Job Reference: 1604-132
Job Duration:
Start date: 01/08/2016
Description:
My client, a German Pharmaceutical company,is currently searching for a Junior Regulatory Manager to join their team based in Dusseldorf, Germany. This is an office basedrole and there will be minimal travel involved. The successful person MUST be fluent in German and English and have a background in EU registrations and CMC.
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 responsibilityas 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.
*3+ 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 +44 (0) 1727 817 626 or email a copy of your CV to tbarratt@keypeople.co.uk
Industry: Pharmaceuticals
Salary: €35000 - €45000 per annum
Salary Benefits:
Vacancy Type: Permanent
Job Skills: regulatory affairs, assistant manager, manager, cmc, germany, pharmaceutical
Contact Name: Tim Barratt
Website: -
Direct Application URL: -