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    About this role

  • Location

    Switzerland

  • Salary

    €140000 - €170000 per annum

  • Type

    Permanent

  • Division

    Pharmaceutical Regulatory Affairs Jobs

  • Reference

    BB - 12268_1595244128

  • Start date

    ASAP

  • Managing this role

Executive Consultant

Brieuc Baeckeroot

+44 203 8540 263

brieuc.baeckeroot@xplorelifescience.com

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

Description

The Regulatory Affairs department is growing in Europe. Building up the team to take over the EU, FDA as well as Canada. You will have a chance to get some diversity and be part to settle, organise the first steps in Europe.

This will open yourself doors for growth, development, that will open opportunities for yourself in the future.

Your tasks:

  • Implement regulatory strategy regarding the region and product.
  • Preparation and planning of the submission working cross-functionally with internal teams, meeting with the health authority…
  • Communicating and coordinating the activity within the group, as well as with external partners.

You will take an important role in the strategy and its application working with different teams in the business (Clinic, quality, CMC…).

Qualifications required:

  • 8 years of experience in Regulatory Affairs having experience with the FDA, EMA, Canada is a bonus
  • Able to define priorities, assess a strategy while respecting the project deadline
  • Having full autonomy, you must be able to solve issues with minimum assistance
  • Speaking German & English

Contact:

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 in the link or by phone: +44 20 3854 0263

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