Regulatory Affairs Manager, Zurich Area

£77060 - £107884 per annum + Bonus
Aug 16, 2018
Sep 15, 2018
Matt Beedle
Organization Type
Clinical Practice
Contract Type
Full Time

Regulatory Affairs Manager, Technical focus on CMC, Stable and long lasting team, Zurich Area

Superb opportunity to join a well established and stable regulatory affairs team with a growing manufacturer in the Pharmaceutical industry. The role will have a focus on technical regulatory affairs covering writing all the way to e-ctd submissions. In addition to this, we expect this person to be a part of a number of different project teams. As such, you will have daily interactions with QA/R&D and manufacturing. This means the role goes beyond just regulatory and as such, leaves people with broad commercial and technical experience in the long term. If you could be interested 'in principle', then please contact me.

Key responsibilities:

  • Ownership of RA activities for CMC, DMF and INDs covering writing to submission
  • Close collaboration with project teams and clients

Key requirements:

  • Experience in hands on CMC for pharmaceuticals (ideally small molecules)
  • Life science background, Chemist ideal
  • Fluency in English, German is a preference, however not a pre requisite

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 . Please refer to for references.

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.

Similar jobs

Similar jobs