Senior Regulatory Writer

Lausanne, Vaud, Switzerland · Regulatory Affairs & Market Intelligence


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:

Senior Regulatory Writing

Reporting to the Global Head of Regulatory Affairs, you will be required to support the Global Regulatory Affairs Associate Directors in the preparation of regulatory documents.

Main responsibilities:


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Debiopharm International can offer you

If you fit this profile please send your application.

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