Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms RSS Feed RSS Feeds

Job Details

Regulatory Affairs CMC GRL, Director Level - This a gloabl role with a growing company in a beautiful part of the world!

Company: Advanced Regulatory (UK & Europe)
Location: Geneva, Switzerland
Reference: TMADV / 280918A
Closing Date: 23 Feb 19
Type: Full Time
Salary (£): On Application
Benefits: On Application

Top Job

Job Summary:

My client is a Geneva based Global Biotechnology company who are looking for a bright and ambitious professional to take the lead on developing global regulatory CMC strategies for early phase projects through global registrations. Contact Theo Moore on + 44 (0) 207 801 3384


Regulatory Affairs Director, CMC GRL – Based in Geneva – EMA & FDA Leadership. Do you want to take the lead for global biological development projects?

Location: Geneva, Switzerland

This highly efficient and extremely successful medium sized Biotechnology company that has developed a hugely impressive pipeline of large molecule biologicals in mid and late stage of development.  There are a number of potential blockbusters due for filling in the EU and USA over the next 1-3 years.   As a result my client is now seeking a highly experienced CMC professional with a biological background gained through experience in either EU or US markets to take the lead in setting global strategies and coordinating  complex submissions for the US, Europe and major international markets.

This is a  highly visible role that requires strong levels of leadership for multiple cross-functional project teams and strong organizational and analytical skills to drive and provide strategic / operational regulatory CMC direction. 

Your duties will include responsibility for leading global CMC regulatory strategy for biologic development  projects which will include HA meetings and negotiations for FDA and EMA.  You will also lead and matrix manage for internal & external teams on assigned projects for the preparation and review of IND/IMPDs, NDA/BLAs and EU and International MAAs.

With this excellent role comes an excellent package which includes: a high level basic salary, bonus, car allowance, full re-location package to beautiful Geneva with expectations that you will take the lead for Global projects.

This a gloabl role, with a  growing company in a beautifal part of the world!


If you wish to apply for this role, please send your CV with a covering note to or alternatively, to have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.

About Advanced

Advanced Regulatory is a division of Advanced Search and Selection Ltd and has been operating since 2004. We are registered and licensed to recruit through the United Kingdom, mainland Europe and the Americas - we have offices both in the UK and in Switzerland. We are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory Affairs.

We match professional candidates to the best permanent, contract and interim roles in the market. For more information about the company visit us at

We provide a high level of service because we believe this matters. Regulatory professionals will find we know our recruitment subject matter.

Keywords / Key words: Regulatory, Regulatory Affairs, Reg Affairs, RA, Regulatory jobs, RA jobs, Regulatory Affairs Jobs. CMC, Bio, Biotechnology, IMP, IMPD, BLA, NDA, EMA, FDA, Regulatory, Regulatory Affairs, Reg Affairs, RA, Regulatory jobs, RA jobs, Regulatory Affairs Jobs. CMC, Bio, Biotechnology, IMP, IMPD, BLA, NDA, EMA, FDA



To Apply : Please send a full CV in confidence to

Contact Information:

Address:  Head Office
Suite 8 Penhurst House 352-356 Battersea Park Road London
SW11 3BY
Tel:  +44 (0)20 7801 3380
Fax:  +44 (0)20 7228 1188
Website:  Visit Our Web Site

Site Map | Privacy & Security | Cookies | Terms and Conditions is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.