Regulatory Affairs Manager, Zurich Area
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.
- Ownership of RA activities for CMC, DMF and INDs covering writing to submission
- Close collaboration with project teams and clients
- 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 firstname.lastname@example.org or call me, Matt Beedle, Regulatory Affairs Consultant for Switzerland on +41435 080817 . Please refer to ch.linkedin.com/in/regulatoryaffairsswitzerland for references.
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