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    About this role

  • Location


  • Salary

    €100000 - €190000 per annum

  • Type


  • Division

    Pharmaceutical Quality Assurance Jobs

  • Reference

    BB - 11775.2_1595865212

  • Start date


  • Managing this role

Executive Consultant

Brieuc Baeckeroot

+44 203 8540 263


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


In charge of a portfolio where you will be developing the regulatory strategy. You will plan, write, and gather the CMC information from the Clinical Trial the drugs already on the market.

Working on an international level, you will be in touch with the FDA and EMA, this scope will give you a wide range of diversity in terms of geographical area as well as phase of the drugs. You will always have something different to work on.

Your tasks:

  • Set up and put in place the strategy for the submission, Variations, and renewals.
  • Work alongside the development teams for the Clinical Trial Application.
  • You will be the point of contact with the health authority: FDA/EMA

An exciting position that will be challenged, you will have an opportunity to start almost from scratch and mark the development of your fingertips.

Qualifications required:

  • 5 years of experience in Regulatory Affairs: CMC
  • Expertise with Biological and on with the FDA & EMA
  • Speaking English and French


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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