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Regulatory Affairs Officer

Pauwels Consulting | Antwerpen | Permanent, Independent, Full-time

Regulatory Affairs Officer

Job description

For one of our pharmaceutical clients in the region of Antwerp, we are looking for a Regulatory Affairs Officer. As a RA Officer, you have the following responsiblities:

  • Keeping up to date with EU procedural requirements and legislation
  • Collaborating closely with national agencies in order to ensure timely approval by national 
  • Ensuring updates to regulatory databases
  • Demonstrates ability to coordinate tasks with others for timely competition and to avoid setbacks
  • Develop training material and deliver training to business end users
  • Liaising with Regional Submission Planner to provide input and ensure alignment on submission plans


As a Regulatory Affairs officer, you have the following strengths:

  • Degree in Life Sciences
  • 1 - 2 years of experience with pharmaceutical Regulatory Affairs (GMP)
  • The ability to review regulatory documents for accuracy
  • Understandig the end-to-end pharmaceutical lifecycle
  • Great communication skills oral and written in English AND Dutch OR French
  • Teamplayer with eye for detail
  • Availabe shortly

For more information, please reach out to


  • Challenging projects based on your interests and skills
  • Personal follow-up and clear, transparent communication both before and after commencement of employment
  • Possibility to follow extra training
  • Inspiring network events and legendary after work drinks
  • Strong network of industry leading clients
  • Expertise within IT, Engineering and Life Sciences
  • A flying start for every junior, growth opportunities and possibility to share gathered knowledge for more senior employees

More info

Bezoek voor meer informatie over de vacature Regulatory Affairs Officer of solliciteer online op de vacature Regulatory Affairs Officer.

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