In the long term you will have the opportunity to grow, lead and manage your own team across development and marketed products whilst gaining EU biotech MAA experience. 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
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. ...
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 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
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. ...
My client organisation is back on the rise again they are now looking for a regulatory affairs manager or senior manager to take the lead in large CMC focused projects through various stages of the development and marketed products lifecycle. This role will suit those who are CMC specialists who like to take the lead on major projects. Contact Theo Moore on +44 207 801 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
My client is looking for an experienced regulatory affairs professional to join their established Regulatory team as a Regulatory Affairs Associate in the South East. This is role is perfect for ambitious people who are looking to join a Global Company with an excellent training and development structure.
My client is looking for an experienced regulatory affairs professional to join their established Regulatory team as a Senior Regulatory Affairs Associate in the South East. This is role is perfect for ambitious people who are looking to join a Global Company with an excellent training and development structure.
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.
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