About this role

  • Posted on

  • Location


  • Salary

    £83289 - £116604.60 per annum

  • Type


  • Division

    Pharmaceutical Regulatory Affairs Jobs

  • Reference

    BB - 12760.5_1601882007

  • Start date


  • Managing this role

Executive Consultant

Brieuc Baeckeroot

+44 203 8540 263


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


You will advise the development teams on the Regulatory strategy and procedures. This will be for Biologic and Pharmaceutical products.

Working closely with the Swissmedic you will have a key role to play. Getting the information from the Swissmedic and advise the Regulatory Teams to adjust, change, or put in place the best strategy possible.

Your task:

  • Alongside the development team, you will advise the local strategy & processes to adopt.
  • Working across regions to provide support in order for them to deliver the product align with the strategy
  • Being the main regulatory liaison between SwissMedic and the group.
  • Provide the resources, knowledge in order to adapt the right strategy and operational regulatory input across the teams.

Your experience:

  • Several years of experience in Regulatory Affairs ideally:
  • Worked within the Biotech and Pharmaceutical products
  • Got strong knowledge of the Development phases to the submission and registration of the product
  • Worked on a local level with the SwissMedic
  • Able to work in cross-functional projects

This is a role where you will be challenged, you will need to have an open mindset to be able to come with solutions for the regulatory teams. If you are up for a new challenge, with a part of the unknown contact me.


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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