Regulatory Affairs Manager A great opportunity for a Regulatory Affairs Manager to step into this strategy role for the EU. Work on ensuring clinical trial approvals for one or more of my client’s products as well as marketed approval for medicinal products. ...
My leading Biopharmaceutical client is looking for an experience and motivated CMC bio senior manager to take the lead on a number of projects. You will be working with an excellent pipeline in a strong team, where the focus is on high level strategic input. Call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380 - or Andrew Barnes in our Swiss office, on +41 41 710 5100
***Regulatory Affairs Senior Manager CMC Biologics *** Basel, Switzerland *** Provide Strategic leadership for CMC bio projects *** Excellent pipeline *** Contact Andrew Barnes in our Swiss Office on +41 41 710 51 00 or Theo Moore on or +44 (0) 207 801 3384
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 email@example.com
Project Manager – Regulatory Affairs (NCEs) – Part home based/Greater London My client, a very well-known and respected consultancy, is looking for an experienced Regulatory affairs professional to join their company. This professional will have 5+years working with New Chemical Entities (NCEs) and managing the whole regulatory process through national and EU procedures. ...
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 discussion about this or other potential roles or career options, French and German speaking candidates should call Marc Van de Voorde in our Swiss office, on +41 (0)78 170 4042 and for candidates from the UK, NL and rest of world call Matt Greig or Theo Moore, in the UK London office, on +44 (0)207 801 3380.
Senior Regulatory Affairs Consultant –Regulatory – Home based The company This company is a top 5 global CRO with a large and ever growing consulting arm. This company is global company with over 10,000 employees across all continents. They are a company that help their clients get medicines into the hands of those who need them most. They offer scientific know how, industry expertise and an outstanding environment to learn and grow. ...
A fantastic opportunity has been made available for a Quality Assurance and Regulatory Affairs professional within the Medical Devices sector. Working on a permanent basis for a specialist consultancy you will have the benefits of both contract and permanent work traits working on project by project basis in a permanent role ensuring you get the excitement of varied roles with the knowledge of a stable role for a growing company.
A fantastic opportunity has been made available for a Quality Assurance and Regulatory Affairs professional within the Medical Devices sector. Working on a permanent basis for a specialist consultancy you will gain extensive visibility within the market place from both small and large companies, ensuring productivity is to the highest standard.
Exciting opportunity for a Regulatory professional to join this global diagnostics company as Regulatory Affairs Manager. You will be required to manage a small UK team and report directly to Global VP Regulatory Affairs in the US.
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