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Job Details

Regulatory Affairs CMC Director – Cover early & late phase dev. projects - Lead EU & US submissions - Switzerland -

Company: Advanced Regulatory (UK & Europe)
Location: Geneva, Switzerland
Reference: TMADV / 301018F
Closing Date: 05 Jan 19
Type: Full Time
Salary (£): On Application
Benefits: On Application

Job Summary:

Work on Global CMC projects and have real autonomy, scope and responsibility for your own varied product portfolio. You will need at least 10 years of Regulatory affairs CMC experience and be ready for a role where you have real autonomy, scope and responsibility for a varied product portfolio, managing multiple products in different stages of development. Call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.

Requirements:

Regulatory Affairs CMC Director – Cover early & late phase dev. projects -  Lead EU & US submissions - South-West Switzerland - Great Salary and full Re-location Packages Available

Advanced Regulatory have a number of new Regulatory Affairs CMC roles based at the Global Head office of one of a dynamic and successful Biotechnology company.

These roles are good mix of strategic input, global project management and cover development and global registration activities. Promotion prospects are very strong and there are options available to become a technical CMC specialist or move into people/team leadership.

You will need to be strong in leading regional CMC strategies through to fulfilment, optimising timelines where possible by working well with cross functional departments and your colleagues in Global (therapy) Regulatory.  You will be the regional lead providing regulatory insight and intelligence on the regions to foster best approaches, from developing regional CMC RA strategies through to the preparation and submission of CMC documentation for development and registration / lifecycle in EU and all major Global regions including being the US lead.

You will need at least 10 years of Regulatory affairs CMC experience and be ready for a role where you have real autonomy, scope and responsibility for a varied product portfolio, managing multiple products in different stages of development

The salary and package is exceptional for this role, including a strong basic salary + Bonus + shares + full re-location package including housing and a large settling in allowance.

If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com 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.
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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 www.advregulatory.com.

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.

To Apply : Please send a full CV in confidence to cv@advregulatory.com.

Contact Information:

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

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