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
Please consider this role! To respond, for French and German speaking candidates should apply to Marc Van de Voorde in our Swiss office, Marc@Advregulatory.com or on +41 (0)78 170 4042 and for candidates from the UK, NL and rest of world to Matt Greig, in the UK London office, to CV@Advregulatory.com or call +44 (0)207 801 3382 / +44 (0)7918 679 405 (eves / w/ends)
This company is highly rated within the industry and is well on itâ€™s way to becoming the worlds No.1 Pharmaceutical Company. The pipeline is rich and diverse, and includes Pharma and Biotech compounds. For this role you will operate as the EU Regulatory liaison for Oncology. 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
An expanding Bio-pharmaceutical company in the Berks/Bucks border is seeking a dynamic personality, with fantastic coms and relationship building skills for Regulatory Affairs Snr EU Manager role where you will lead Product Lifecycle Mgt activities for a Biological portfolio. Contact Theo Moore on 0207 801 3384 or email me in confidence via email@example.com
Within this role you will operate as the EU and ROW regulatory partner reporting into a locally based Global Regulatory leader - If you wish to apply for this role send your CV with a covering note to firstname.lastname@example.org quoting reference number noted above. Alternatively to have a confidential call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380.
An exciting job opportunity with our client, a leading Pharmacuetical company based in Dublin. We are now recruiting for a Core Dossier and EU Submissions Team Leader to join the team.
In conjunction with the Core dossier and EU submissions Manager you will assist in the departmental processes for EU products and brands. This role will require a proven track record in Core dossier and EU submissions and Team Supervision
Regulatory Affairs EU Region Lead
Buckinghamshire. Due to expansion and a new budget for the New Year, a leading pharmaceutical company in Buckinghamshire are seeking to recruit a Regulatory Affairs EU Region Lead for their team. This is a permanent position offering a competitive salary and benefits, located in Buckinghamshire just outside of Greater London. This company mainly specialises in Medical Devices, however this role would be focused on the pharmaceutical side of Regulatory Affairs.
My expanding pharmaceutical client with offices and success worldwide is seeking a Regualtory Affairs Senior Manager with a sound knowledge of European pharmaceutical regulations and guidelines and a proven track record in drug development, to take the lead for a Centralised filing and to get involved in Global Regulatory strategies. This role has everything to keep you excited and motivated for many years to come.
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