Regulatory CMC Specialist, Vibrant Growing Pharma

Cambridge, United Kingdom

Reference	MB/66796/2
Contract type	Permanent

Regulatory Affairs CMC Specialist, Cambridge, Small Molecules

Join a developing department where you will have significant input into CMC submissions on a global basis. It is a superb opportunity to use your experience in CMC and be involved in the CMC development of many life saving drugs. In addition to this, you will be based in some of the best facilities the UK has to offer!

Benefits:

* Highly reputable company with great staff retention.
* Opportunity to step into global CMC and work on a number of variations
* Work across a range of highly innovative small molecule products

Responsibilities:

* Liaise with regulatory bodies and affiliates
* Have scientific and operational input into CMC submissions with cross over with manufacturing and quality assurance
* Coverage for IMPD/IND submissions

Requirements:

* Ideally over1 years experience within regulatory CMC for the pharmaceutical or bio-tech industry
* EU or MHRA experience is required
* A life science degree or associated qualification

For a confidential discussion about this role or to inquire about regulatory affairs in Switzerland, then send your CV to m.beedle@nonstop-recruitment.com or call me, Matt Beedle, Regulatory Affairs Consultant 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 mind 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

5/23/13 2:50 PM

comments powered by Disqus