In the long term you will have the opportunity to grow, lead and manage your own team across development and marketed products whilst gaining EU biotech MAA experience. If you wish to apply for this role send your CV to firstname.lastname@example.org or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380 - or Andrew Barnes in our Swiss office, on +41 41 710 5100
If you have over 7 years Regulatory CMC experience for development or supporting MAA's and are now looking for a great next challenge, then this could be the role for you. If you wish to apply for this role send your CV to email@example.com or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380 - or Andrew Barnes in our Swiss office, on +41 41 710 5100
This position is ideal for those looking for a role which will focus on CMC but still allow you to work through the full project lifecycle for both Pharma and Biotech projects. If you have 1-3 years RA experience with a focus on CMC and want to gain expansive project management experience then this is going to be the role for you. Contact Theo Moore on 0207 801 3384.
Director Regulatory Affairs - Post Approval - CMC Bias
Middlesex. Some flexibility for home working after probation period
The client: Has a 40% turnover outside the US and Europe has approved over six significant new product approvals in 2013 alone. Our client's innovative medicines, vaccines and consumer products enable millions of people to do more, feel better and live longer. They discover, make and market life-enhancing products on a global scale.
My client organisation is back on the rise again they are now looking for a regulatory affairs manager or senior manager to take the lead in large CMC focused projects through various stages of the development and marketed products lifecycle. This role will suit those who are CMC specialists who like to take the lead on major projects. Contact Theo Moore on +44 207 801 3384
CMC Director *** Lead industry initiatives across Europe for top 10 PharmaCo *** Based in Germany | Please call Theo Moore Matt Greig on +44 (0)207 801 3384 or direct on +44 (0)7918 195 166 (eves / weekends). Alternatively you can email me on theo@AdvRegulatory.com
*** Be the CMC Regulatory lead and provide in-depth working knowledge of CMC and regulatory procedures, legislation and guidelines for submissions applicable to biotechnology and products across EU and Emerging Markets. Call Andrew Barnes in our Swiss office on +41 41 710 51 00 or Theo Moore in the UK office on +44 (0) 207 801 33 84
My Basel based leading Biopharmaceutical company is seeking an exceptional CMC candidate with Excellent working knowledge/experience in regulatory submissions and approval processes for New Chemical Entities (NCE) and product life cycle management and proven practical knowledge of and ability to deal with complex CMC regulatory issues and requirements. Contact Theo Moore on +44 (0)207 801 3384 or send your CV in confidence to firstname.lastname@example.org
If you wish to apply for this role send your CV with a covering note to email@example.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options, French and German speaking candidates should call Marc Van de Voorde in our Swiss office, on +41 (0)78 170 4042 and for candidates from the UK, NL and rest of world call Matt Greig or Theo Moore, in the UK London office, on +44 (0)207 801 3380.
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