Associate Director, Global Regulatory Affairs

Lausanne, Vaud, Switzerland · Regulatory Affairs & Market Intelligence

Description

Debiopharm Group™ (Debiopharm) is a Swiss-based biopharmaceutical group of five companies active in drug development, GMP manufacturing of proprietary drugs, diagnostics, and investment management. Debiopharm International SA searches, evaluates and in-licenses promising drug candidates for development. Towards the end of the development process, the products are licensed out to pharmaceutical companies for worldwide marketing and sales. For our Regulatory Affairs Department based in Lausanne, we are looking for a:

Associate Director, Global Regulatory Affairs

Reporting to the Global Head of Regulatory Affairs, you will be a core-team member within a matrix organization and will be actively involved in the development of therapeutic medicines from POC through approval or out licensing (whichever comes first) thereby contributing to strategy of the drug development path as well as to compliance with applicable regulations.

Main responsibilities

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Debiopharm can offer

If you fit this profile please send your application.

For more information : www.debiopharm.com

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