About this role

  • Posted on

  • Location


  • Salary

    €55000 - €75000 per annum

  • Type


  • Division

    Pharmaceutical Regulatory Affairs Jobs

  • Reference

    BB - 12427.5_1599119536

  • Start date


  • Managing this role

Executive Consultant

Brieuc Baeckeroot

+44 203 8540 263


Source Group International GmbH, Bosch 106, 6331 Hunenberg, Switzerland


Following the acquisition of new products in development the team has been built up recently.
After discovering potential new applications, you will help to define and plan the Regulatory strategy since the early phases.

This is an interesting and challenging opportunity by the nature of the project which is new for the company. This will leave you a room to bring your expertise but also develop your skills and open yourself to new opportunities.

Your task:

  • Support the Associate Director and Global Regulatory Affairs in order to deliver the approvals and up to date information.
  • Define the strategy for the early phases of the development and communicate it across the teams part of the project
  • Gather the information needed from other departments: Clinical, Quality, Regulatory to meet the deadline.

Your experience:

  • 3/5 Years of experience in the Pharmaceutical Industry (CRO, HQ or Affiliate)
  • Experience with the Development phase especially in the early phases
  • You have worked with EU regulation
  • English speaking, French OR Flemish are a bonus

The project will be full of challenges, however, this is a great place to grow, develop new skills that will set up your next career steps. Working with an interesting and unique project that will passionate yourself.


Feel free to reach me even if the position is not exactly what you are looking for.
Please share it with your network or any person you think you might be interested in.

You can send me your CV, Resume with your contact details through the link OR you can contact me on Linkedin.

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