Regulatory CMC Expert, Zug, Switzerland, 120k+

Zug, Switzerland

Reference	MB/620099/6
Contract type	Permanent

Regulatory CMC Expert, Zug, Switzerland, 120k+

CMC Expert, Range of Therapy Areas, English Speaking, Variation between QA and Regulatory Departments, Zug

Become the CMC expert/ go to person for CMC for an upcoming start up company with a number of established products on the market. The role will be focused on submissions and writing for CMC for the FDA. Due to this being a smaller company your duties will be broad from mentoring junior staff to coverage of change control, aspects in QA and working closely with supply chain.

Company Information:

A relatively new company in Switzerland who are taking on a range of new products for 2013. Enjoy a pro active atmosphere where your work is recognised and you will have the change to meet and work with some of the most senior people in the company. If you have previously worked in big Pharma then this is a great chance to be exposed to a greater variety of responsibilities in a company where your progress will be in your own hands. In addition to this the company is growing giving you great scope for progress.

Role Responsibilities:

* Be the go to person within the department for CMC requirements
* Prepare and write CMC submissions
* Work closely with QA and Supply chain departments

Role Requirements:

* At least 3 years experience in regulatory CMC including CMC writing
* High level in English

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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