Posted to MedZilla on 9/23/2018

Phaidon International

US-, Senior Regulatory affairs specialist 452431215476-MZ


 
 


Our client, a midsize Pharmaceutical company very successful in  the development of new therapies in Metabolic disease is looking for a Senior Regulatory affairs specialist to join their team in the south of France. The senior Regulatory affairs specialist will join great facilities and an experienced team working on different projects.

 
Key responsibilities

 The regulatory affairs specialist will be mainly in charge of submission and regulatory. The senior regulatory affairs specialist will also be in charge of market authorization and CMC.

Desired Skills and experienc
  • Past experience in Regulatory Affairs
  • Minimum professional experience: 5+ years or equivalent
  • Fluent in French; Good knowledge of English
  • Self motivated and organised
  • Experience in Marketing authorisation process
 
Qualifications
  • University degree in Medical Science or/and Pharmacy
 

To apply for the Senior Regulatory Affairs Specialist role please send a word copy of your CV to:

[click here]">[click here]
gregoire.laurent(at)epm.phaidonschweiz.ch
+41 44 542 12 81

 

EPM Scientific is a trading arm of Phaidon International GmbH. Freigutstrasse 26, 8002 Zürich, Switzerland. No féd. CH-660-0972012-8


Please visit our website at www.phaidoninternational.com

 
 


* If a direct employer requests that you go to their web site and complete your application there in order to be
  considered, please do so. Applications for all positions are subject to each employer's specific requirements.