Posted to MedZilla on 6/28/2017


Phaidon International

US-, Specialist Regulatory affairs - Medical Device - Europe 452431215676-MZ


 
 

Our client, a midsize Medical Device company is looking for a Regulatory affairs Specialist based who will be based in the Netherlands. The Regulatory affairs Specialist will be joining a well established Medical Device company with proven knowledge and good results. The Regulatory affairs Specialist will have growing opportunities inside the company in the upcoming years.

 
Key responsibilities

The Regulatory affairs Specialist will be in charge of process leading to Marketing Authorization. The Regulatory affairs Specialist will not be managing a team, but should be able to work inside a team as well as on his own. The Regulatory affairs Specialist will be working closely with the company affiliates in Europe as well as with Government agencies.

Desired Skills and experience

  • Past experience in Regulatory affairs is mandatory
  • Minimum 1-2 years experience or equivalent
  • Fluent in English, Any other European Language a big plus
  • Experience working in multicultural environment
  • Experience in Medical Device or strong interest/knowledge
  • Technical or Life Science Degree
 
KEY WORDS: Regulatory affairs; Specialist Regulatory affairs; Medical Device; Cardiology; Cardiovascular; Netherlands; Europe; PMA; ISO 13485; 510K; CE mark; Spanish; English; Pharmaceutical industry; team;

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

[click here]">[click here]
gregoire.laurent(at)epm.phaidonschweiz.ch
+41 44 208 3775

 

 


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.