Senior Regulatory Manager, Top Level Pharma!
Basel, Switzerland
| Reference | MB/62009c/9 |
| Contract type | Permanent |
Join a developing department where you will have significant input into CMC strategy and submissions on a global basis. It is a superb opportunity to use your experience in CMC to mentor junior staff while being involved in the CMC development of many life saving drugs. In addition to this, you will be based in some of the best facilities Switzerland has to offer at the heart of the world's pharmaceutical industry.
Benefits:
* Relocation package
* Opportunity to step up in management
* Work across a range of highly innovative small molecule products
Responsibilities:
* Liaise with regulatory bodies and affiliates
* Mentor junior staff
* Have scientific and operational input into CMC strategy from manufacturing to regulatory submissions
* Project management for a range of products
Requirements:
* Ideally over 6 years experience within regulatory CMC for the pharmaceutical or bio-tech industry
* EU experience is required, experience with the FDA or Emerging markets is beneficial
* A life science degree or associated qualification
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 | 5/23/13 2:57 PM |
Please note that if you are not a passport holder of the country for the vacancy you might need a work permit. Check our Blog for more information.
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