Regulatory Affairs Manager, CMC
Regulatory Affairs (Senior) Associate, CMC, Fast Paced Global Regulatory Team, Both Pre and Post Approval CMC
Join one of the most successful regulatory teams in Germany with development options across Europe. One key point to mention about this position is the opportunity to work across multiple therapy areas and product types, with this in mind we typically see people learn a lot in a very short period of time. The company are growing rapidly due to a very competitive business model which is taking much of Europe by storm. I strongly recommend this role to regulatory candidates who are career minded and want to extend their experience in regulatory affairs. The team are global and have a good mix of people from all over the world. If you could be interested in principle then please feel free to contact me.
- Writing and review of CMC documents for Pharma products
- Pre and post approval product responsibilities
- Responsible for key client interactions and scientific inputs
- At least 2 years experience in regulatory affairs
- A life science degree
- Fluency in English
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 on +41435 080817 .For regular job updates and market information please join my regulatory affairs linked-in group. https://www.linkedin.com/groups/4550988
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.
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