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Regulatory Affairs Labelling Manager

Regulatory Affairs Labelling Manager - Switzerland - Permanent

Our client is a global speciality Pharmaceutical company with a broad variety of products on the market and in late phase development. They are currently seeking a Regulatory Affairs Labelling Manager to join their friendly team.

Key Responsibilities:

* Develop the optimum labelling strategy for a range of products
* Develop and manage processes for the creation, in-house approval and implementation of labelling documents
* Organise and lead the cross-functional Global Labelling Team to reach consensus on global labelling matters and the preparation of supporting documents
* Coordinate and manage projects on a tmely manner
* Support the global implementation including guidance and advice to affiliates and partners.

QUALIFICATIONS COMPETENCES

Essential
* Professional technical training in the field of pharmaceutics, chemistry, biology or other life sciences or university diploma
* Experience in the field of International regulatory affairs and/or the pharmaceutical industry
* Ability to work in a computerized environment, with good knowledge of Microsoft Office, Internet, databases etc

Preferred
* Expertise in a registration discipline such as toxicology, safety, efficacy and or/labelling
* German Language skills


Key Words: Global labelling, labelling, regulatory affairs, regulatory affairs manager, pharmaceuticals, labelling strategy, regulatory projects, Switzerland, European, Europe, german

We are dedicated to the clinical research industry, offering candidates a unique service including our free \"Pipeline Watch\" career advisory consultation. To find out more call us on 0118 9594990 or email apply@clinicalprofessionals.co.uk