Regulatory Affairs Associate, Pharmaceuticals

Regulatory Affairs Associate, Pharmaceuticals, Zurich Region

I am currently working with one of the fastest growing pharmaceutical companies in Europe who are looking to expand their capabilities in regulatory affairs. With this rapid expansion and many pending submissions, there is now the opportunity for someone to join the regulatory affairs team. Critically we will be looking for someone to assist on CP submissions to the EMA. Given this, it is the chance to be a part of what is expected to be a successful MA submission. The repercussions of this from an experience point of view is clearly highly attractive! Please contact me for more information.

Key Responsibilities:

• Supporting the regulatory affairs team on key submissions
• Project management of fillings and requirement goals
• Help on basic regulatory intelligence inquiries

Key Requirements:

• Life science degree
• Currently based in Switzerland
• Experience in pharma regulatory affairs ranging from 1 year+

For a confidential discussion about regulatory affairs, or to apply, then send your CV to m.beedle@nonstop-recruitment.com 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. https://www.linkedin.com/groups/4550988

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 ch.linkedin.com/in/regulatoryaffairsswitzerland for references.