Regulatory Affairs Manager, Switzerland + Relocation

Switzerland, Switzerland

Reference	MB/62310/1
Contract type	Permanent

Regulatory Affairs Manager CMC, Switzerland, International, Development, Biopharmaceutical, 130k+

This is a fantastic opportunity to work in a leading biologics department at the heart of a global pharmaceutical company. In this position you will have a significant role in the preparation and submission of documents from early development to post approval in CMC. In addition to this, there is a strong emphasis on international submissions.

Role Benefits:

* A highly varied position that will allow you to gain the experience required to develop your career to the very top in regulatory affairs
* The chance to use your scientific background in conjunction with regulatory affairs
* Work on international projects allowing you to expand your experience outside of the EU.

Role Responsibilities:

* Preparation of pre and post marketing sections for CMC
* Work along side regulatory bodies
* Project manage and provide regulatory support
* Train junior staff

Role Requirements:

* Life science degree
* Ideally over 4 years experience in regulatory affairs CMC

For a confidential discussion about regulatory affairs in Switzerland, or to apply, then send your CV to m.beedle@nonstop-recruitment.com or call me, Matt Beedle, Regulatory Affairs Head Hunter for Switzerland on +41 435 0808 17

I am a specialist head hunter 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 market as well as ATMP(Advanced Therapeutics) and biological regulatory professionals world wide.

If you are a regulatory affairs professional looking for your next opportunity, then please contact me. Alternatively if you are currently looking for skilled individuals for the development of your organisation then I can certainly help.

NonStop is the fastest growing pharmaceutical recruitment firm in Europe and is already one of the biggest! We have offices in the UK, the Czech Republic and in Zug, Switzerland. We uniquely receive EU funding and with this in mnd we meet some of the most stringent quality control measures in the industry.

What I offer:
A high level of knowledge of regulatory affairs recruitment, therefore not just finding you suitable roles but in addition to this, I do not waste your time.

Specialties:
*Switzerland Regulatory Affairs Market with a focus on German speakers
*Biologics EU wide
*ATMP, ATP, AT, Advanced Therapeutics, World Wide
*Recruitment at all levels including associate, manager, senior manager, associate director, director, global director, senior director and vice president.

Expires on

5/24/13 5:00 AM

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