My client is a successful Brussels based Pharmaceutical Company focused on developing medicines for un-met medical needs, and continues to grow and develop at an extraordinary rate. They have ambitions to one day become a top ten pharmaceutical company and are offering fantastic opportunities to work on global development projects. Please contact Theo Moore on +44 (0)207 801 3380 or email your Cv in confidence to Theo@advregulatory.com
Join an organisation that is ready to take the lead in Biosimilars. You will pay an extremely important and integral role in the Biosimilars Regulatory department for an organisation that is ready to take the lead in this category. Contact Theo Moore on +44 (0) 207 801 3384 or send your CV to Theo@advregulatory.com
Join an organisation that is ready to take the lead in Biosimilars. You will pay an extremely important and integral role in the Biosimilars Regulatory department for an organisation that is ready to take the lead in this category. 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 UK London office, on +44 (0)207 801 3380 or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
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
Regulatory Affairs Associate CMC
Permanent. Berkshire. Office-based
Our client is one of the largest OTC pharmaceutical companies in the UK and due to pipeline there are recruiting for a Regulatory Officer\Associate to be based from their offices in Berkshire. In the last 10 years our client have trebled their revenue and in the top 25 of companies listed on the London Stock Exchange.
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.
Premier Research are a growing global CRO focused on delivering high quality clinical research projects to their diverse client base. With industry leading expertise in Paediatrics, Analgesia, Oncology and CNS we are looking for career focused individuals who want to be a part of our growth.
***The role will require you to lead regional CMC strategies through to fulfilment, optimising timelines where possible by working well with cross functional departments and your colleagues in Global Regulatory and Global RA CMC***
Call Theo Moore on +44 (0)207 801 3384 or email me in confidence at firstname.lastname@example.org
Assisting in the preparation of high quality biopharmaceutical CMC submissions for global regulatory agencies. Providing technical regulatory expertise in assessing proposals for manufacturing change (change controls) affecting clinical development biopharmaceutical products. Assisting technical teams in appropriately communicating information within technical reports that may form part of regulatory submissions.
My client is looking for a regulatory professional with 15 years experience who is ENTHUIASTIC, PRO-ACTIVE & AMBITIOUS to lead & drive forward the companiesâ€™ regulatory function. This is a newly created position due to a reorganisation of the business.
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