Global Regulatory Affairs Manager, Geneva
Global Regulatory Affairs Manager, Rx Drugs Pre and Post Approval, Fast Growing Global Pharma, Geneva, Switzerland
Excellent opportunity to join a vibrant regulatory affairs team in an expanding global pharmaceutical company. The role comes about due to a number of new product acquisitions and approvals meaning there is much needed help to manage products and to help sustain regulatory affairs with upcoming pipeline products. What makes the role interesting is that it covers full life cycle activities, including pre and post approval, submissions, health authorities and CMC. In addition to this there is scope to work with commercial aspects and across teams such as QA and sales. With this in mind, it is a good position for someone wanting to expand their skill set in RA.
Regarding the client, they have had significant growth and as a bi-product of this there are good long term opportunities within the teams. In addition, it's a highly commercial and fast paced environment and can be an excellent move for someone who may be working in a set role in big pharma. If you could be interested 'in principle', then please contact me for more information.
* Full LCM activities from pre to post approval of key products
* Part of cross functional teams
* Working on worldwide submissions including EMA
* Working with vendors and external alliance partners
* Life science degree
* Over 4 years regulatory affairs experience in Pharmaceuticals (Rx)
* Experience managing post marketed products
* Fluency in English, French and other languages would be a bonus
* Holder of an EU passport
For a confidential discussion about regulatory affairs, or to apply, then send your CV to email@example.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
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