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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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📑 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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📑 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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📑 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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📑 CMC Project Manager Remote £55K-£70KViral respiratory tract infections make up a huge percentage of reported illnesses in the UK. In a recent study conducted by ONS, 1 in 6 people surveyed had a viral respiratory tract infection!Would you like to be part of a team trying to tackle this monumental issue?A rare opportunity has arisen to join a biotec ...

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📑 CMC Project Manager Remote £55K-£70KViral respiratory tract infections make up a huge percentage of reported illnesses in the UK. In a recent study conducted by ONS, 1 in 6 people surveyed had a viral respiratory tract infection!Would you like to be part of a team trying to tackle this monumental issue?A rare opportunity has arisen to join a biotec ...

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📑 CMC Project Manager – Pharmaceutical – 12 Months - £500p/d (Inside of IR35) – Stevenage Multi-national leading consumer healthcare client (FTSE100) now requires a Clinical Project Manager to ensure CMC Project Plans are designed and executed in line with meeting time, cost, and quality.You will be responsible for generating scenario planning for th ...

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📑 CMC Project Manager – Pharmaceutical – 12 Months - £500p/d (Inside of IR35) – Stevenage Multi-national leading consumer healthcare client (FTSE100) now requires a Clinical Project Manager to ensure CMC Project Plans are designed and executed in line with meeting time, cost, and quality.You will be responsible for generating scenario planning for th ...

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📑 We are seeking a highly motivated Clinical Supply Chain Manager that thrives in a fast-paced and dynamic environment while working on multi-disciplinary teams. The Supply Chain Manager (SCM) role provides strategic oversight of the end-to-end supply chain for assigned GSK R&D investigational assets. The SCM is accountable for determining supply st ...

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📑 Clinical Supply Chain Consultant - Operations United Kingdom Req #2339 Monday, November 27, 2023 Clinical Supply Chain Consultant This could be the Opportunity of Your Life! Want to make a difference? Interested in working with high-end health technology and using your organization ...

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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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📑 Overview At the heart of QIAGEN’s business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many ...

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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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📑 We are seeking a highly motivated Clinical Supply Chain Manager that thrives in a fast-paced and dynamic environment while working on multi-disciplinary teams. The Supply Chain Manager (SCM) role provides strategic oversight of the end-to-end supply chain for assigned GSK R&D investigational assets. The SCM is accountable for determining supply ...

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📑 Senior Manager – global Clinical Supply Chain Operations£90 per hour (experience dependent) + min 12-month contract with excellent possibility of permanent opportunity thereafter + immediate start available + 100% remote working + collaborative global team environmentSenior Manager – global Clinical Supply Chain Operations responsibilities ...

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📑 Senior Manager – global Clinical Supply Chain Operations£90 per hour (experience dependent) + min 12-month contract with excellent possibility of permanent opportunity thereafter + immediate start available + 100% remote working + collaborative global team environmentSenior Manager – global Clinical Supply Chain Operations responsibilities ...

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📑 We are currently looking for a Senior Regulatory Affairs Officer to join a leading Pharmaceutical company based in the Kent area. As the Regulatory Affairs Manager, you will play a pivotal role in managing the life cycle and post-authorisation changes for products within the UK, focusing on CMC, clinical, safety, and product information modificatio ...

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📑 We are currently looking for a Senior Regulatory Affairs Officer to join a leading Pharmaceutical company based in the Kent area. As the Regulatory Affairs Manager, you will play a pivotal role in managing the life cycle and post-authorisation changes for products within the UK, focusing on CMC, clinical, safety, and product information modificatio ...

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📑 Role Overview We are currently looking for a Senior Regulatory Affairs Officer to join a leading Pharmaceutical company based in the Kent area. As the Regulatory Affairs Manager, you will play a pivotal role in managing the life cycle and post-authorisation changes for products within the UK, focusing on CMC, clinical, safety, and product inf ...

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📑 Viral respiratory tract infections make up a huge percentage of reported illnesses in the UK. In a recent study conducted by ONS, 1 in 6 people surveyed had a viral respiratory tract infection! Would you like to be part of a team trying to tackle this monumental issue? A rare opportunity has arisen to join a biotech start- ...

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📑 Logistics Manager, Permanent, £28000 - £32000 per annum, 28 days leave, pension, parkingOur client is looking for a highly experienced Logistics Manager who specialises in imports and exports specifically around USA, Poland, and Germany.The Logistic Manager will collaborate with both the sales team and accounts department to ensure supplies are del ...

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📑 Role Overview We are currently looking for a Senior Regulatory Affairs Officer to join a leading Pharmaceutical company based in the Kent area. As the Regulatory Affairs Manager, you will play a pivotal role in managing the life cycle and post-authorisation changes for products within the UK, focusing on CMC, clinical, sa ...

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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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📑 RRxCo is partnered with a Biotechnology organisation developing immunotherapies in the Oncology arena. With a presence in the United Kingdom, Europe and the United States, you will join a leading development team dedicated to the development of Immunotherapies to treat various cancer types. You will be required to build and lead the foundations & i ...

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📑 RRxCo is partnered with a Biotechnology organisation developing immunotherapies in the Oncology arena. With a presence in the United Kingdom, Europe and the United States, you will join a leading development team dedicated to the development of Immunotherapies to treat various cancer types. You will be required to build and lead the foundations & i ...

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📑 Driven by our purpose of safeguarding life, property, and the environment, DNV enables organisations to advance the safety and sustainability of their business. We provide classification and technical assurance along with software and independent expert advisory services to the maritime, oil & gas and energy industries. We also provide certific ...

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📑 Career CategoryRegulatoryJob DescriptionIf 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 togethe ...

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📑 PATH is currently recruiting for a CMC Technical Officer to provide tactical and operational support for the Polio vaccine project. Responsibilities Process Development, Scale up, Technology Transfer Coordinate the technology transfer of viral vaccine manufacturing processes between m ...

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📑 Coalesce Management Consultancy (CMC) have an consulting assignment available for a Senior Software Developer to work on a project in the North East. Join our latest projectCurrently we’re looking for a Software UI Developer to work on a project we have with a client based in the North East. They have an end client who are looking to engage with s ...

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📑 Coalesce Management Consultancy (CMC) have an consulting assignment available for a Senior Software Developer to work on a project in the North East. Join our latest projectCurrently we’re looking for a Software UI Developer to work on a project we have with a client based in the North East. They have an end client who are looking to engage with s ...

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📑 We are currently looking for a Senior Analytical Chemist to join a leading developing Gene Therapy company based in London. As the Senior Analytical Chemist you will be responsible for the driving the development of analytical assays for AAV product and process characterisation.This opportunity would suit a Scientist with subject matter expertise i ...

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📑 We are currently looking for a Senior Analytical Chemist to join a leading developing Gene Therapy company based in London. As the Senior Analytical Chemist you will be responsible for the driving the development of analytical assays for AAV product and process characterisation.This opportunity would suit a Scientist with subject matter expertise i ...

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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 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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📑 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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📑 About The Role UNLOCK YOUR BEST WORK LIFE + make a difference for every patient Due to the increase in the patient care we provide, we have an opening for a Supplies Administrator to join our close-knit supplies team based at of Emerson’s Green Hospital, Bristol. Do you have administration experience within a stores, warehouse, proc ...

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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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📑 PPD is a leading global contract research organization. At PPD we are passionate, deliberate, and driven by our purpose - to improve health. PPD’s Clinical Management department is committed to industry leadership and the relentless pursuit of excellence. Working in the Clinical Management department, you will combine deep knowledge, the ...

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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 ...

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📑 Coalesce Management Consultancy (CMC) have a consulting assignment available for a Site Manager to work on a 50MW BESS project in the Stoke on Trent area.CMC provide expert engineering solutions on an international capacity for Engineering and other Renewable Energy projects. Established in 2016, we set out our mission to be the best service-driven ...

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📑 Coalesce Management Consultancy (CMC) have a consulting assignment available for a TP137 Site Manager to work on a 400kV National Grid project in the West London area.CMC provide expert engineering solutions on an international capacity for Engineering and other Renewable Energy projects. Established in 2016, we set out our mission to be the best s ...

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📑 Coalesce Management Consultancy (CMC) have a consulting assignment available for a TP137 Site Manager to work on a 400kV National Grid project in the West London area.CMC provide expert engineering solutions on an international capacity for Engineering and other Renewable Energy projects. Established in 2016, we set out our mission to be the best s ...

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