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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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📑 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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📑 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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📑 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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📑 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 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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📑 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, with a focus on biotechnology products. The suc ...

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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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📑 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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📑 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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📑 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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📑 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 ...

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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 ...

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📑 Your newpany A global biopharmaceuticalpany focusing on rare diseases is looking for a CMC consultant toe in to cover maternity leave for 12 months.Your new role You will be responsible for Regulatory CMC support for post-approval submissions formercial biological products, and new international MAA fillings fo ...

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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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📑 Regulatory Affairs Consultant.8+ years' experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresLead and / or co ...

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📑 Your newpany A global biopharmaceuticalpany focusing on rare diseases is looking for a CMC consultant toe in to cover maternity leave for 12 months.Your new role You will be responsible for Regulatory CMC support for post-approval submissions formercial biological products, and new international MAA fillings for the EU.What you'll need to succeed A ...

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📑 Regulatory Affairs Consultant.8+ years' experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market.Good understanding of regulatory framework, including regional trends, for various types o ...

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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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📑 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 and review) of CMC documentation and sections for regulat ...

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📑 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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📑 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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📑 A well-funded startup in the biotechnology sector specializing in ophthalmology. As a leader in developing innovative products, our mission is to protect and restore the vision of patients suffering from various eye diseases. We are expanding our Chemistry, Manufacturing, and Controls (CMC) team to support our ocular therapies into late-phase clini ...

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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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📑 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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📑 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 regions, (Asia, Latin Amer ...

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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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📑 Job PurposeAs a Senior Manager, Regulatory Affairs CMC, you are an integral part of MoonLake’s Clinical Development team responsible for the development, execution and tracking of regulatory CMC and medical device activities.You will be responsible for the development of a CMC and device regulatory strategy, working closely with Technical Operation ...

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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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📑 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 ne ...

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📑 Position: Regulatory Affairs CMC Manager Location: Holborn, LondonContract Length: Initial 12 Months - possibility to extend Work Structure: Monday - Friday (onsite or remote flexibility)Pay Rate: £700 - 730/day Are you a seasoned Regulatory Affairs CMC Manager with a wealth of experience in the bio-pharmaceuticals Industry? We are seeking a skille ...

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📑 Position: Regulatory Affairs CMC Manager Location: Holborn, LondonContract Length: Initial 12 Months - possibility to extend Work Structure: Monday - Friday (onsite or remote flexibility)Pay Rate: £700 - 730/day Are you a seasoned Regulatory Affairs CMC Manager with a wealth of experience in the bio-pharmaceuticals Industry? We are seeking a skille ...

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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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📑 Job PurposeAs a Senior Manager, Regulatory Affairs CMC, you are an integral part of MoonLake’s Clinical Development team responsible for the development, execution and tracking of regulatory CMC and medical device activities.You will be responsible for the development of a CMC and device regulatory strategy, working closely with Tec ...

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📑 i-Pharm Consulting are recruiting for an experienced Biologics CMC (drug substance/drug product or analytics) Project Leader for a global health group operating in the vaccine development field. The role would initially be offered as a 12 month fixed term contract, with a potential to be made permanent. You can be based in the UK, East Coast of US ...

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📑 i-Pharm Consulting are recruiting for an experienced Biologics CMC (drug substance/drug product or analytics) Project Leader for a global health group operating in the vaccine development field. The role would initially be offered as a 12 month fixed term contract, with a potential to be made permanent. You can be based in the UK, East Coast of US ...

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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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📑 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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📑 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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📑 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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📑 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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📑 Head of Regulatory AffairsAre you looking for a role to lead global regulatory filing strategy?Do you have recent experience of regulatory strategy for novel oncology modalities?Have you worked on programs from preclinical stage to filing and launch?Fraser Dove International is partnering exclusively with an innovative biotechnology organisation sp ...

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