An opportunity has arisen for an experienced Regulatory Affairs CMC Emerging Markets specialist with a growing Global BioPharmaceutical company with an exciting and varied pipeline of products. You will be responsible for strategically ensuring that the preparation of Regulatory submissions for commercial products in multiple emerging markets according to regional litigation and company policies and procedures.
This is great role with enough scope to keep you interested and enough development opportunities to allow you to continue to grow as a regulatory professional. 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 Marc Van de Voorde in our Swiss office, on +41 41 710 5100
There is an excellent salary available for this role (up to 110,000 Euros) and this position also offers a fully expensed Car, Attractive Bonus, Shares and a Full- Re-location Package. If you wish to apply for this role send your CV to email@example.com or call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380 or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
My client is a successful Brussels based Pharmaceutical Company focused on developing medicines for un-met medical needs, and continues to grow and develop at an extraordinary rate. They have ambitions to one day become a top ten pharmaceutical company and are offering fantastic opportunities to work on global development projects. Please contact Theo Moore on +44 (0)207 801 3380 or email your Cv in confidence to Theo@advregulatory.com
Senior Manager Global Regulatory Affairs CMC opportunity available on a permanent basis in Cambridge, my client is a leading Global BioPharmaceutical company with a great reputation in the market place for their innovative and ethical approach; they are also offering an excellent salary and benefits package for this highly innovative and visible role in their Global Regulatory Affairs CMC team.
Leading UK based Biopharmaceutical company is looking for a Regulatory affairs CMC Manager and Snr Manager to operate as the EU CMC product lead supporting regulatory activities for various biotechnology and chemically-derived commercial (marketed) and development (clinical) products. Contact Theo Moore +44 (0) 207 801 3384
Regulatory Affairs CMC Director
Are you a highly experienced Regulatory Affairs CMC candidate? If so, I am currently recruiting for a CMC Director position with one of the top global pharmaceutical companies, based in Hertfordshire.
This is a permanent role offering a salary of cÂ£80,000 plus a benefits package including a 15% annual bonus and car allowance.
Gold Group is seeing a significant increase in activity in the Regulatory Affairs arena within the Pharmaceuticals and Device market and below you will see a snapshot of the opportunities I have available.
(31196) Reg Affairs Director â€“ London - Â£80,000â€“ Â£90,000 - Perm We are looking to experienced Director to provide strategy and expert advice within the biopharmaceutical industry. ...
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
PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her