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.
Regulatory Affairs Associate with developed CMC experience is required to join a Global BioPharmaceutical company in the South East on a permanent basis. My client has a great reputation for their ethical and dynamic approach along with the fantastic career development they offer. The Regulatory Affairs Associate CMC will work under general supervision and gain exposure to European and International markets throughout the entire product life-cycle.
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 email@example.com 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 firstname.lastname@example.org 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
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.
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
Our client is a Global leader and pioneer in the Biotechnology field using innovative research to drive the discovery and development of important therapeutics. This top company has a strong development pipeline with strong prospects in Oncology, Osteoporosis and Renal. They are currently seeking a Regulatory Affairs Associate, CMC for a 12 month contract based either in South East UK or East Anglia.
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.
As Senior Regulatory Affairs Associate, responsibility will be covering lifecycle activity within the EU, Emerging and African regions for a blockbuster product and other specialist therapy areas. Including; the preparation, submission and review of CTAs, MAAs, IMPD, PIPs. This role will suit a candidate with relevant experience looking for an organisation to develop within.
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