This is a great opportunity to join a company which has shown an excellent levels of growth and has a promising future - If you wish to apply for this role send your CV to cv@advregulatory.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
Operate as the Global Regulatory Lead and/or EU Regulatory Lead on a global Life Cycle Team or Marketed Product Team for complex and/or business critical projects for a leading Bio-Pharmaceutical based in Switzerland. This role comes with a strong team and strong portfolio of both Pharma and Biological products. Contact Theo Moore on +44 (0)207 801 3384
You will receive excellent promotion prospects and those who achieve good levels of success in EU submissions will quickly be promoted into a Global position. If you wish to apply for this role send your CV to cv@advregulatory.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
Learn how to provide leadership for regulatory submissions whilst providing strategic and innovative thinking for major pharms and biotech projects/submissions (for EU and/or International territories) - If you wish to apply for this role send your CV to cv@advregulatory.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
My client is a highly successful and expanding a Bio-Pharmaceutical company with an extensive pipeline and a high value commercial portfolio who is seeking a dynamic, innovative and highly motivated personality to take the lead for EU (and sometimes Global) Regulatory strategies and submissions. This role comes with an excellent salary; full–relocation package & excellent career prospects. Contact Theo Moore on +44 (0) 207 801 3384
Regulatory Affairs Manager - Switzerland
Basel or Geneva, office-based. An exciting opportunity has arisen for an experienced Regulatory Affairs Manager looking for a new, diverse challenge in Regulatory Affairs. My client, a global pharmaceutical company is looking for a Manger to provide leadership to a team of associates and consultants, provide a variety of consulting services, and to work within project guidelines to achieve project objectives and address client issues.
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 cv@advregulatory.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
As your experience grows, so will your level and depth of project responsibility, ultimately leading to you becoming a Global regulatory leader with responsibility for your project in all major regions (EU/US/Asia/LatAm). If you wish to apply for this role send your CV to cv@advregulatory.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
Join a global biotech organisation at their Global HQ in Switzerland where you will be offered excellent career opportunities, favorable development and the chance to lead EU or International biotech strategies and submissions.
Contact Theo Moore or Matt Greig on +44 207 801 3384 or email your CV to CV@advregulatory.com
This is a highly visible role where you will lead from the front on development, strategy and agency interaction. The pipeline is exceptional you will be working from the Global Head office.
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