Senior Regulatory Affairs Manager, 80-100%

5 days left

£80148 - £100185 per annum + Bonus
Sep 28, 2016
Oct 28, 2016
Matt Beedle
Organization Type
Clinical Practice
Contract Type
Full Time

Senior Regulatory Affairs Manager, 80-100%

This is an exciting opportunity to join a relatively new Pharmaceutical company looking to actively grow their RA team. You will have the chance to work on high level products that are well known in Switzerland while also working on new submissions to Swissmedic. With this in mind you should be working on a variety of projects, allowing you to learn, have autonomy and gain experience in areas such as QA and PV. Ideal for someone with regulatory experience at the local level in Switzerland, who wants to gain greater autonomy, with more scope and future opportunities!

Key responsibilities:

  • Become RP for Swiss products
  • Main contact with Swissmedic for all submissions and meetings
  • Preparation of regulatory documents for submission to Swissmedic
  • Management of 1 member of staff


  • Life Science Degree
  • Experience in regulatory affairs for Pharma/OTC/Biotech
  • Ideally experience on regulatory submissions to Swissmedic
  • Fluency in German

For a confidential discussion about regulatory affairs, or to apply, then send your CV to or call me, Matt Beedle, Regulatory Affairs Consultant for Switzerland on +41435 080817. For regular job updates and market information please join the Switzerland regulatory affairs linked-in group.

I am a specialist head hunter(recruiter) for regulatory affairs in the Pharmaceutical & Biotechnology industry. I offer a number of search options within the industry with a special focus on the Swiss regulatory affairs market as well as ATMP(Advanced Therapeutics) and biological regulatory professionals world wide. Please refer to for references.

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