Regulatory Affairs CMC Associate Manager Job; a global biopharmaceutical organisation with a solid commercial portfolio of life saving drugs within a number of therapy areas is seeking a CMC Regulatory Affairs professional. They have a pipeline full of exciting and novel therapies both small and large molecules.
Due to continued expansion they are seeking an experienced CMC strategist for the post of Associate Manager. ...
My client is a global biopharmaceutical company specializing across a number of areas of medical need for serious diseases. They are looking to appoint a senior level CMC professional at Associate Director Level for full strategic input into both new filings and the extensive commercial portfolio of drugs in EU and RoW markets.
You will have extensive regulatory expertise in CMC and will ideally have worked on major EU filings for new products in the past. ...
This position is ideal for those looking for a role which will focus on CMC but still allow you to work through the full project lifecycle for both Pharma and Biotech projects. If you have 1-3 years RA experience with a focus on CMC and want to gain expansive project management experience then this is going to be the role for you. Contact Theo Moore on 0207 801 3384.
Als Regulatory Affairs Associate betreuen Sie verschiedene Projekte, die sich mit der Erstellung von QualitĂ¤tsdokumenten befassen. Weiterhin arbeiten Sie an dem CMC Teil fĂĽr nationale und internationale Zulassungen. AuĂźerdem stehen Sie mit den ZulassungsbehĂ¶rden in Kontakt und vertreten das Unternehmen.
Regulatory Affairs Associate / West London / CMC Module 3: - My client is a successful and well funded global pharmaceutical organisation. This is a unique role that will give the successful candidate the opportunity to work on both Bio & Pharma products in a role that will clearly excel your regulatory affairs career.
Title: EU CMC RA Associate Director (Head of CMC Regulatory)
At a glance: Most senior CMC role in company, managing, EU and RoW CMC, ethical and branded.
Please call Matt Greig or Theo Moore +44 (0)207 697 7303 (eves & weekends call +44 (0)7918 679 405).
If you have over 7 years Regulatory CMC experience for development or supporting MAA's and are now looking for a great next challenge, then this could be the role for you. 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 - or Andrew Barnes in our Swiss office, on +41 41 710 5100
Are you looking to gain regulatory affairs experience in both Pharma and Biotech Projects??? Do you want to develop your EU project management experienceâ€¦.???? then read on as this could be the role for youâ€¦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
This position is ideal for those looking for a role which will focus on CMC but still work through the full project lifecycle for both Pharma and Biotech projects. If you have 1-3 years RA experience with a focus on CMC and want to gain expansive project management experience then this is going to be the role for you. Contact Theo Moore on 0207 801 3384
Senior Regulatory Affairs Associate
Wiltshire (work from home 1 day per week)
Salary & benefits: Up to ÂŁ45,000
Our client is fast growing pharmaceutical company who specialise in respiratory product development. They have an opportunity for a Senior Regulatory Affairs Associate to be based from their offices in Wilshire.
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