📑 Associate Director, Regulatory Affairs CMC/ Senior Manager Hertfordshire, UK An exciting opportunity to join an established pharmaceutical company that specialises in Oncology and Neurology. The role will be working across both portfolios and will have a heavy focus on regulatory strategy. As a Regulatory Affai ...
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📑 Our client, a successful and growing Biotechnology organisation, is looking to hire a new addition to the Regulatory CMC team.This role is responsible for preparing regulatory CMC submission strategy for rare disease drugs (both biologics and small molecules) and an opportunity to design creative solutions in order to obtain approval for initial BL ...
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📑 Our client, a successful and growing Biotechnology organisation, is looking to hire a new addition to the Regulatory CMC team.This role is responsible for preparing regulatory CMC submission strategy for rare disease drugs (both biologics and small molecules) and an opportunity to design creative solutions in order to obtain approval for initial BL ...
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📑 Job Title: Regulatory Affairs – Senior CMC Dossier ManagerJob Type: Contract position until December 2024, inside IR35Rate: Up to £85ph PAYE or UmbrellaLocation: UK or Europe (Remote-based)CPL has partnered with a world-leading Biotech looking for an experienced Regulatory CMC leader to work on a developing rare disease portfolio. This will be supp ...
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📑 Job Title: Regulatory Affairs – Senior CMC Dossier ManagerJob Type: Contract position until December 2024, inside IR35Rate: Up to £85ph PAYE or UmbrellaLocation: UK or Europe (Remote-based)CPL has partnered with a world-leading Biotech looking for an experienced Regulatory CMC leader to work on a developing rare disease portfolio. This will be supp ...
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📑 Job Introduction Thanks for checking out our vacancy, we’re delighted you want to learn more about Dechra.Here at Dechra, our values are embedded within our culture and thrive within our family of more than 2000 colleagues globally. From manufacturing to marketing, ( D )edication, ( E )njoyment, ( C ) ...
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📑 PE Global is currently recruiting for a Regulatory Affairs CMC Manager for a contract role with a leading multinational Biotech client based in London – Fully remote within the UK.Regulatory CMC support for post-approval submissions for commercial products, predominantly biotechnology products and new international MAA filings predominantly in EMEA ...
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📑 PE Global is currently recruiting for a Regulatory Affairs CMC Manager for a contract role with a leading multinational Biotech client based in London – Fully remote within the UK.Regulatory CMC support for post-approval submissions for commercial products, predominantly biotechnology products and new international MAA filings predominantly in EMEA ...
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📑 Proclinical is seeking a Regulatory CMC Associate for a 12-month contract role. This position will provide support to the Chemistry, Manufacturing and Controls (CMC) function, which is responsible for Module 3 of regulatory submissions across various phases of product development, from clinical to lifecycle. The role involves organising, managing, ...
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📑 Regulatory Affairs Consultant CMC, biologics outside of IR35Your new companyThis growing US rare disease company is looking for an experienced Regulatory Affairs CMC (biologics) professional to join them on a 12-month contract, this contract job is outside of IR35 and can be fully remote or hybrid working.Your new roleAs Regulatory Affairs Consulta ...
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📑 Proclinical is seeking a Regulatory CMC Associate for a 12-month contract role. This position will provide support to the Chemistry, Manufacturing and Controls (CMC) function, which is responsible for Module 3 of regulatory submissions across various phases of product development, from clinical to lifecycle. The role involves organising, managi ...
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📑 Walker Cole International are looking for a CMC Regulatory Affairs Director to join an established Pharmaceutical Business in the UK. In this role you will be responsible for the development and execution of CMC regulatory strategy for the business.As the CMC Regulatory Affairs Director, you will be responsible for: * The developme ...
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📑 Walker Cole International are looking for a CMC Regulatory Affairs Director to join an established Pharmaceutical Business in the UK. In this role you will be responsible for the development and execution of CMC regulatory strategy for the business.As the CMC Regulatory Affairs Director, you will be responsible for: * The developme ...
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📑 Description The GRS-CMC organization provides regulatory expertise related to CMC activities through all stages of a products lifecycle. Members of the organization develop global regulatory CMC strategies and partners with key stakeholders to execute the strategies in alignment with business priorities. The team also perform regulatory asse ...
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📑 If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that read over 10 m ...
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📑 Description The GRS-CMC organization provides regulatory expertise related to CMC activities through all stages of a products lifecycle. Members of the organization develop global regulatory CMC strategies and partners with key stakeholders to execute the strategies in alignment with business priorities. The team also ...
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📑 Walker Cole International is supporting one of its clients in their search for a Chief Quality Officer. The business have a diverse portfolio of established and pipeline assets and are currently undergoing growth due to acquisitions.As the Chief Quality Officer, you will drive a corporate quality structure, oversee an international team across seve ...
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📑 Walker Cole International is supporting one of its clients in their search for a Chief Quality Officer. The business have a diverse portfolio of established and pipeline assets and are currently undergoing growth due to acquisitions.As the Chief Quality Officer, you will drive a corporate quality structure, oversee an international team across seve ...
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📑 Are you looking for a role where you will serve as a key strategic partner representing Global Regulatory activities? If so, this Director of Regulatory Affairs, CMC could be an exciting opportunity to explore. This role will provide strategic direction and guidance on both global project and key strategic business initiatives. Within Global Reg ...
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📑 Senior Regulatory Consultant - Remote - Contract Proclinical is actively seeking a Senior Regulatory Consultant. This is a remote contract position. Primary Responsibilities: This role primarily involves providing regulatory CMC support for post-approval submissions for commercial products, wi ...
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📑 About UsExscientia is an AI-driven pharmatech company committed to discovering, designing and developing the best possible drugs in the fastest and most effective manner. Exscientia developed the first-ever functional precision oncology platform to successfully guide treatment selection and improve patient outcomes in a prospective interventional c ...
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📑 About UsExscientia is an AI-driven pharmatech company committed to discovering, designing and developing the best possible drugs in the fastest and most effective manner. Exscientia developed the first-ever functional precision oncology platform to successfully guide treatment selection and improve patient outcomes in a prospective interventional c ...
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📑 Are you looking for a role where you will serve as a key strategic partner representing Global Regulatory activities? If so, this Director of Regulatory Affairs, CMC could be an exciting opportunity to explore. This role will provide strategic direction and guidance on both global project and key strategic business initiatives. Wi ...
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📑 Are you looking for a role where you will serve as a key strategic partner representing Global Regulatory activities? If so, this Director of Regulatory Affairs, CMC could be an exciting opportunity to explore. This role will provide strategic direction and guidance on both global project and key strategic business initiatives. Wi ...
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📑 About UsExscientia is an AI-driven pharmatech company committed to discovering, designing and developing the best possible drugs in the fastest and most effective manner. Exscientia developed the first-ever functional precision oncology platform to successfully guide treatment selection and improve patient outcomes in a prospective ...
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📑 About UsExscientia is an AI-driven pharmatech company committed to discovering, designing and developing the best possible drugs in the fastest and most effective manner. Exscientia developed the first-ever functional precision oncology platform to successfully guide treatment selection and improve patient outcomes in a p ...
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📑 RRxCo. has an exciting project with a Life Science organisation that requires a Regulatory Consultant. This fully remote project involves taking an innovative vaccine through from early-stage development to commercial, as the main regulatory lead. You will provide both strategic and hands-on input.Contact me if you have the below and are set up as ...
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📑 RRxCo. has an exciting project with a Life Science organisation that requires a Regulatory Consultant. This fully remote project involves taking an innovative vaccine through from early-stage development to commercial, as the main regulatory lead. You will provide both strategic and hands-on input.Contact me if you have the below and are set up as ...
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📑 Description KEY RESPONSIBILITIES The Senior Director, CMC Regulatory Affairs Policy, Advisory and Intelligence is a recognized expert both inside and outside the business, and is responsible for leading various aspects of internal and external-facing advocacy as applicable to support the Gilead portfolio. This leader will represent the bu ...
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📑 Description KEY RESPONSIBILITIES The Senior Director, CMC Regulatory Affairs Policy, Advisory and Intelligence is a recognized expert both inside and outside the business, and is responsible for leading various aspects of internal and external-facing advocacy as applicable to support the Gilead portfolio. This leader will represent the bu ...
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📑 Description KEY RESPONSIBILITIES The Senior Director, CMC Regulatory Affairs Policy, Advisory and Intelligence is a recognized expert both inside and outside the business, and is responsible for leading various aspects of internal and external-facing advocacy as applicable to support the Gilead portfolio. This leader will represent the bu ...
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📑 Job DescriptionGeneral Summary:The Chemistry Manufacturing Controls Manager will influence the execution of multi-product global regulatory CMC strategies for marketed products. This role contributes to the preparation and submission of regulatory CMC documentation and with interactions with Health Authorities for CMC topics. This role also provide ...
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📑 Job title: Associate Director, Regulatory Affairs A Pharmaceutical business in London is looking for an Associate Director, Regulatory Affairs to join their Global team. In this role you will provide strategic regulatory and scientific assessment on preclinical requirements, and clinical development plans to bring new products to patients in the mo ...
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📑 Job title: Associate Director, Regulatory Affairs A Pharmaceutical business in London is looking for an Associate Director, Regulatory Affairs to join their Global team. In this role you will provide strategic regulatory and scientific assessment on preclinical requirements, and clinical development plans to bring new products to patients in the mo ...
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📑 Description KEY RESPONSIBILITIES The Senior Director, CMC Regulatory Affairs Policy, Advisory and Intelligence is a recognized expert both inside and outside the business, and is responsible for leading various aspects of internal and external-facing advocacy as applicable to support the Gilead portfo ...
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📑 Description KEY RESPONSIBILITIES The Senior Director, CMC Regulatory Affairs Policy, Advisory and Intelligence is a recognized expert both inside and outside the business, and is responsible for leading various aspects of internal and external-facing advocacy as applicable to support the Gilead portfo ...
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📑 Description KEY RESPONSIBILITIES The Senior Director, CMC Regulatory Affairs Policy, Advisory and Intelligence is a recognized expert both inside and outside the business, and is responsible for leading various aspects of internal and external-facing advocacy as applicable to support the Gilead portfo ...
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📑 Make your mark for patients We are looking for a Regulatory CMC Scientist – Small Molecules to join us in our Regulatory Affairs team, based in any of the following locations: Brussels (Belgium) or Slough (UK) About the role Define the strategy, planning and preparation (writing ...
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📑 Job DescriptionGeneral Summary:The Chemistry Manufacturing Controls Manager will influence the execution of multi-product global regulatory CMC strategies for marketed products. This role contributes to the preparation and submission of regulatory CMC documentation and with interactions with He ...
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📑 Regulatory Affairs CMC Manager - Remote - Contract Proclinical is seeking a Regulatory Affairs CMC Manager to support global commercial post-approval submissions. This is a remote contract position. Primary Responsibilities: This role involves working closely with regulatory CMC and cross-functional teams to ensure the successful executi ...
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📑 Regulatory Affairs Consultant CMC, biologics outside of IR35Your newpany This growing US rare diseasepany is looking for an experienced Regulatory Affairs CMC (biologics) professional to join them on a 12-month contract, this contract job is outside of IR35 and can be fully remote or hybrid working.Your new role As Regulatory Affairs Consultant CMC ...
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📑 Tax Manager / Tax Associate Director - Outskirts of Manchester - £Negotiable dependent on level and experience & Excellent BenefitsDescription:Are you a qualified Senior Tax Professional with extensive experience in both corporate and private client tax?Are you looking for an opportunity to take your career to the next level with a firm that offers ...
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📑 Location: London, Greater London, United Kingdom Type: Contract Job #25229 Are you an experienced Regulatory Affairs professional with a background in Chemistry, Manufacturing and Controls and experience working in the Biopharmaceutical/Biotechnology industry, and are you looking for a new opportunity? We have your next role, we ar ...
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📑 Regulatory Affairs CMC Manager - Remote - Contract Proclinical is seeking a Regulatory Affairs CMC Manager to support global commercial post-approval submissions. This is a remote contract position.Primary Responsibilities:This role involves working closely with regulatory CMC and cross-functional teams to ensure the successful execution of commerc ...
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📑 Regulatory Affairs CMC Manager - Remote - Contract Proclinical is seeking a Regulatory Affairs CMC Manager to support global commercial post-approval submissions. This is a remote contract position.Primary Responsibilities:This role involves working closely with regulatory CMC and cross-functional teams to ensure the successful execution of commerc ...
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📑 We are looking for: Interim Director of Quality Assurance/QP position to develop, manage and implement quality strategies within Pharmaron Hoddesdon across its CMC activities to ensure that the strategies are aligned with corporate and regulatory authority requirements. The role will entail maintaining the Hoddesdon Quality Assurance function, as ...
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📑 Regulatory Affairs Consultant CMC, biologics outside of IR35Your newpany This growing US rare diseasepany is looking for an experienced Regulatory Affairs CMC (biologics) professional to join them on a 12-month contract, this contract job is outside of IR35 and can be fully remote or hybrid working.Your new role As ...
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📑 Regulatory Affairs CMC Manager - Remote - Contract Proclinical is seeking a Regulatory Affairs CMC Manager to support global commercial post-approval submissions. This is a remote contract position. Primary Responsibilities: This role involves working closely with regulatory CMC and cross-func ...
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📑 My client is a global biopharma company. They are seeking a Regulatory Affairs Manager (CMC) to join our Regulatory Affairs Team based in Cambridge on a 12 month contract. Hybrid working Key Responsibilities Co-ordinate the preparation of high quality CMC documents to support regulatory submissions in International r ...
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📑 When our values align, there's no limit to what we can achieve. Are you an experienced regulatory professional looking for a new opportunity? We are currently seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team! This is a client dedicated project, and the role can be office or home based in va ...
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