Regulatory Affairs Officer

Regulatory Affairs Officer

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Region

Antwerp

Reference

23256

Responsibilities of the Regulatory Affairs Officer

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

Profile of the Regulatory Affairs Officer

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 florian.schatteman@pauwelsconsulting.com

Offer for the Regulatory Affairs Officer

  • 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