Posted to MedZilla on 10/18/2017


Phaidon International

US-, Regulatory affairs Specialist - Croatia/Serbia 452431217206-MZ


 
 

Our client, a well-established Pharmaceutical company 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 for companies in Europe.
 

Key responsibilities

The regulatory affairs specialist will be mainly in charge of submission and regulatory. The regulatory affairs specialist will also be in charge of  PMA,  market authorization and CMC.  The regulatory affairs specialist will be working within in a team in the Regulatory affairs department with also regular contacts with Quality Assurance and Drug Safety staff.

Desired Skills and experience

  • Past experience in Regulatory Affairs
  • Minimum professional experience: 2+ years or equivalent
  • Fluent in English; Other European language a plus
  • Self motivated and organised
  • Experience in Marketing authorisation process, CMC and PMA

Qualifications
  • University degree in Medical Science or/and Pharmacy or Technical degreee
 

KEY WORDS: Regulatory Affairs; Regulatory Affairs Specialist; Senior Regulatory affairs Specialist; Quality assurance, Croatia; Serbia; Zagreb; Belgrade; Drug safety; Us Pharma company; RA; QA; Regulatory affairs Manager

 

To apply for the 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

 
 


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  considered, please do so. Applications for all positions are subject to each employer's specific requirements.