Forward thinking client which is rated in the Top 10 of world Pharmaceutical companies - Excellent Benefits package which includes a great salary & benefits package - Strong pipeline with Oncology, CNS, Pain, Inflammation and Cardiovascular products in late phases of development - Location: Switzerland, Basel, NeuchÃ¢tel, Geneva,
In the first instance please call Matt or Theo on +44(0)207 801 3384 or +44 (0) 7918 195 166 or please send a full CV to Theo@advregulatory.com
About the role This is your chance to join a company that unites people across the world through its unique and innovative product line of medical devices! Be part of a small but truly global company, with manufacturing plants in Switzerland and the US and a presence in 3 of the world's major continents.
I have a new and exciting regulatory affairs role for a Top 20 Pharmaceutical client in Brussels who is looking for a forward thinking regulatory affairs professional who would like to learn how to take the lead for EU development and Centralised MAA projects. Contact Theo Moore on +44(0)207 801 3384 or to apply email me on Theo@advregulatory.com
This role will give you full hands on Centralised procedure submissions experience then allow you to move into a global role. This really is an excellent opportunity to develop your expertise in a friendly & commercially focused environment for one of the worlds fastest growing Pharma companies.
The Salary for this role is up to Â£50,000 with a bonus and highly rated benefits 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 London office on +44 (0)207 801 3380
This organisation has a healthy pipeline of early and late stage development projects and the regulatory department is uniquely set-up in such a way that you will have full project responsibility and leadership for your own Centralised registrations. 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
A regulatory affairs role covering Europe (EU and non-EU countries), Asia Pacific, Latin America, Middle East, Russia and CIS countries, North America and Africa. Cover projects at different stages of drug development ranging from products in clinical development (Phases I to IV) to approved products. Excellent salary, bonus and re-location available. Contact theo Moore or Matt Greig on +44 207 801 3380
Regulatory Project Manager â€“ UK/Ireland/Malta team
Permanent / Bedfordshire
Are you a regulatory professional seeking to take the next step up in your career within Regulatory Affairs? Brand new Regulatory Project Manager role available in Bedfordshire, working in the UK team!
Our client are looking for an experienced Regulatory Affairs professional who has experience of working with medical devices and combination products. You will gain a senior project management position, where you will be working on a range of international projects. This is a secure permanent role that is offering a good competitive salary.
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