Are you a regulatory affairs freelancer within the medical device sector? Are you available to start a new contract with short notice? Apply now without delay to this regulatory affairs freelancer role with a market leading medical device client based in Baar, Switzerland. This is a fast moving role with the opportunity to work on innovative and market leading medical device products over a rolling contract period. We look forward to hearing from you today!
Entrust Clinical People are currently hiring for an immediately available Quality Engineer for our global pharmaceutical and medical device client which distributes medical products and technologies for advanced medical procedures. This is a temporary contract initially running from now until end of November 2014, with a potential view to extension, based out of Salzburg.
Regulatory Affairs “CMC ” EU & Global CONTRACT Roles – up to £75 per hour – Small and Large molecule roles available…!!! 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 is an excellent role where you will be joining a pro-active and highly regarded Regulatory operations team for a leading global Pharmaceutical company based in Berkshire / M4 corridor 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
Freelance Regulatory Affairs Project Manager\ Consultant
Duration: 12-24 month rolling contract. Clinical Professionals are currently recruiting for an exciting new opportunity for a leading Pharmaceutical business based in Germany, Ireland or Switzerland. My client is seeking a Regulatory Affairs Consultant for a freelance opportunity paying a very competitive hourly rate.
A great fixed term contract within regulatory affairs has come in with a world leading medical device company based in the Solothurn area. This is a great opportunity to work with innovative medical devices across a two year period, allowing to lead an interesting and varied working life. If you are a regulatory affairs professional within the medical device industry and available for a new engagement ensure you apply now.
I am currently working with one of the world’s leading Medical Device organisation with a wide variety of innovative Medical Device products and medical technologies working across multiple therapeutic areas. A true global leader within their field and they are always expanding the countries they operate in and distribute to.
Genpact Pharmalink is currently recruiting for a Regulatory Affairs Professional/Consultant at the Associate Director level.
You will head up an international project with both strategic and operational components.
Acting as a primary contact for Pharmalink and the Client, yours is a key integral role and requires a strategic thinker, who is detail oriented and possesses solid regulatory skills.
If you wish to apply for this role send your CV with a covering note to email@example.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options call Matt Greig or Theo Moore, in the UK London office, on +44 (0)207 801 3380.
My client is flexible on working conditions and are happy for people to be in the office 1 day a week or 2 days every fortnight. 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 Andrew Barnes in our Swiss office, on +41 41 710 5100
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