Posted to MedZilla on 12/12/2018

Phaidon International

US-, Regulatory Affairs Manager - BioTech - Paris 452431214537-MZ


 
 


Our client, a fast growing biopharmaceutical company, is looking for a Regulatory affairs Manager with experience working in Marketing authorization submission. The company is currently developing anti-viral compounds and therapeutic vaccines. The Regulatory affairs Manager  will be joining a experienced  multicultural team in France. The Regulatory affairs Manager  will be reporting directly to the Regulatory affairs VP.

Key responsibilities

The Regulatory affairs Manager will be responsible for the following of the process leading to Marketing authorization. The Regulatory affairs Manager will be working closely with CRO on an international  level and should have international or Regional experience in Regulatory affairs. The Regulatory affairs Manager will act direct advisor to the Regulatory affairs VP.

Desired Skills and experience

  • Past experience in Regulatory affairs is mandatory
  • Minimum 5-6 years experience or equivalent
  • Fluent in English, French would be a plus
  • Experience working in multicultural environment and international experience
  • Experience in vaccine or HIV industry would be a plus
 
KEY WORDS: Vaccines; rare disease, haematology; Europe; France; Biotech; Pharmaceutical company; Regulatory affairs; Regulatory affairs Manager; anti-viral compounds, therapeutic vaccines; VP Regulatroy affairs; Quality Assurance; Pharmacovigilance

To apply for the Regulatory affairs 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

 
 


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