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Responsible for execution of new product registration, maintenance of existing medicinal product licences. Interacts with EURMEA regulatory affairs groups, EURMEA clinical groups, EURMEA Clinical Safety, Global Clinical and Regulatory Affairs, R&D and EURMEA business leaders.
Responsible for execution of new product registration, maintenance of existing medicinal product licences. Interacts with EURMEA regulatory affairs groups, EURMEA clinical groups, EURMEA Clinical Safety, Global Clinical and Regulatory Affairs, R&D and EURMEA business leaders.
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The Regulatory Affairs Manager is required to provide regulatory advice on strategy and manage projects in the provision of Regulatory Affairs Services. To liaise with internal and external clients in the provision of marketing these services.
Senior Regulatory Affairs Manager My client is looking for a Senior Regulatory Affairs Manager to join there expanding team. Based in their HQ in Hampshire / Wilshire office. \n\r Role Responsibilities The Regulatory Affairs Manager will be responsible for the planning, execution and maintenance of Marketing Authorisation Applications globally.
My client is a highly regarded global CRO based in Oxfordshire. Due to a successful year the company is expanding and they require an additional Regulatory Affairs Officer to join there team.
My client is a leading global health care company We are a global, broad-based health care company devoted to discovering new medicines, new technologies and new ways to manage health. They are looking for an experience individual to join growing team as the Regulatory Affairs Project Manager.
My client is looking for an experience Regulatory Affairs Operations Associate to join there successful CRO. The company has seen huge success and growth over the last 12 months and is now looking to recuit additional Associates.
To apply for this Head of Regulatory Affairs role please call Julie Cooper on 020 8305 9733 or 07951 082482 Alternatively please send your CV to: julie@mosaicrecruitment.
My client is searching for a Regulatory Affairs Manager to join their team, reporting directly in to the VP of Medical & Regulatory Affairs. \n\r MAIN PURPOSE: The Regulatory Affairs Manager is responsible for planning and managing all regulatory activity associated with a business unit as well as the UK and Ireland product portfolio.
Due to continued success throughout the last 12 months the company is further expanding, my client is looking for X2 experienced Regulatory Affairs Associates to work in their leading global CRO.
My client is looking for a highly experience Regulatory Affairs Specialist to join there organisation. With an urgent requirement the position is available immediately to the right candidate. With over 30,000 employees around the world this is a truly global and very well recognised Pharma company.
My client is looking for a strong all round Regulatory Affairs Manager with at least 8 years’ experience in the pharma field. Key strength would lie with CMC, clinical trial applications, MAA and emerging markets, business development and the experience for being a strong manager.
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