Regulatory Affairs Officers (2)

For one of our clients in the area of Brussels (North-West) we are urgently looking for enthusiastic RA professionals. 

  • Do you have experience in Regulatory Affairs?

  • Are you communicative, conscientious and quality-minded?

  • Do you have a good knowledge of languages (English, French and/or Dutch)?

Take a look at this opportunity; the next step in your career is only one click away!

Job Description 

As a Regulatory Affairs (RA) Professional you play a crucial role in the lifecycle of a medicine, you guide the drug through all phases of development.

Responsibilities 

The Regulatory Affairs Officer controls and approves packaging material, notifications and general regulatory affairs work.  
This includes:

  • Evaluation, drafting, submission and follow-up of variations (Belgian registrations)
  • Preparation and follow-up of renewals
  • Answering questions from authorities
  • Management of various databases
Profile 
  • You have at least 4 year of experience in the Regulatory Affairs
  • You have at least a Bachelor degree (Life Sciences)
  • You have a sound knowledge of EU regulatory procedures and development of medicinal products in general.
  • You have strong communication skills
  • You have a good knowledge of languages (ENG, NL and/or FR)
  • You have good organizational skills, proven ability to multi-task and an excellent eye for details
Contact Information 

Nele Daems
nele.daems@valesta.com
015 21 11 04

 

 

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