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Head of Regulatory Affairs
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Cambridge, Cambridgeshire, United Kingdom BioTalent Full timeJob Title: Head of Quality Assurance and Regulatory Affairs Location: Hybrid About Us: This company is at the forefront of the personalized medicine revolution. They are a dynamic and innovative company dedicated to optimizing the treatment of chronic diseases through a unique approach that combines precision medicine, digital health, and data analytics....
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Regulatory Affairs
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Cambridge, Cambridgeshire, United Kingdom BioTalent Full timeJob Title: Head of Quality Assurance and Regulatory Affairs Location: Hybrid This company is at the forefront of the personalized medicine revolution. They are a dynamic and innovative company dedicated to optimizing the treatment of chronic diseases through a unique approach that combines precision medicine, digital health, and data analytics. I am...
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Regulatory Affairs
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Cambridge, Cambridgeshire, United Kingdom BioTalent Full timeJob Title: Head of Quality Assurance and Regulatory Affairs Location: Hybrid This company is at the forefront of the personalized medicine revolution. They are a dynamic and innovative company dedicated to optimizing the treatment of chronic diseases through a unique approach that combines precision medicine, digital health, and data analytics. I am...
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Regulatory Affairs Director
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Regulatory Affairs Manager
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Cambridge, United Kingdom Reed Full timeQuality Assurance and Regulatory Affairs Lead Location: Hybrid – need to be able to attend the Cambridge siteHours: 37.5 hoursSalary: Competitive and will depend on experience Reed Scientific have partnered with an industry leading Biotech at the forefront of diabetes research. My client has an immediate requirement for someone to lead the quality and...
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Regulatory Affairs Director
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Regulatory Affairs Director
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Cambridge, Cambridgeshire, United Kingdom Lifelancer Full timeJob DescriptionJob Title: Director, Global Regulatory Affairs, OncologyJob Summary:We are seeking an experienced and skilled Director, Global Regulatory Affairs, Oncology to join our team at Lifelancer. As a key member of our organization, you will be responsible for developing and executing regulatory strategies for our assigned programs and products.Key...
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Regulatory Affairs Director
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Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeJob SummaryWe are seeking a highly skilled Regulatory Affairs Director to join our team at Gilead Sciences International, Ltd. as a Director, Global Regulatory Affairs, Precision Medicine.Key ResponsibilitiesDevelop and execute precision medicine regulatory strategies in alignment with the company's global regulatory strategy.Collaborate with...
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Regulatory Affairs Director
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Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeJob SummaryWe are seeking a highly skilled Regulatory Affairs Director to join our team at Gilead Sciences International, Ltd. as a Director, Global Regulatory Affairs, Precision Medicine.Key ResponsibilitiesDevelop and execute precision medicine regulatory strategies in alignment with the company's global regulatory strategy.Collaborate with...
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Regulatory Affairs Director
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Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeJob Summary:Gilead Sciences International, Ltd. is seeking an experienced Regulatory Affairs professional to join our team as an Associate Director, Regulatory Strategy. This role will be responsible for providing strategic guidance and oversight to our in-market partners in the Gilead Patient Solutions (GPS) region, ensuring compliance with regulatory...
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Regulatory Affairs Director
2 weeks ago
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeJob Summary:Gilead Sciences International, Ltd. is seeking an experienced Regulatory Affairs professional to join our team as an Associate Director, Regulatory Strategy. This role will be responsible for providing strategic guidance and oversight to our in-market partners in the Gilead Patient Solutions (GPS) region, ensuring compliance with regulatory...
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Regulatory Affairs Senior Manager
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Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeJob Title: Senior Manager, Regulatory Affairs CMCAbout the Role:Gilead Sciences International, Ltd. is seeking a highly skilled and experienced Senior Manager, Regulatory Affairs CMC to join our team in Cambridge, United Kingdom. As a key member of our CMC Regulatory Affairs International Affiliate Team, you will be responsible for ensuring compliance with...
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Regulatory Affairs Senior Manager
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Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeJob Title: Senior Manager, Regulatory Affairs CMCAbout the Role:Gilead Sciences International, Ltd. is seeking a highly skilled and experienced Senior Manager, Regulatory Affairs CMC to join our team in Cambridge, United Kingdom. As a key member of our CMC Regulatory Affairs International Affiliate Team, you will be responsible for ensuring compliance with...
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Regulatory Affairs Program Director
2 hours ago
Cambridge, Cambridgeshire, United Kingdom ProductLife Group Full timeRegulatory Affairs Program DirectorWe are seeking a highly skilled Regulatory Affairs Program Director to join our team at ProductLife Group. As a key member of our Regulatory Affairs department, you will be responsible for piloting and managing Regulatory Affairs outsourcing projects/programs for major clients.About the RoleYou will act as a direct point of...
Regulatory Affairs Manager
4 months ago
CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Cambridge, on a contract basis for 12 months. Company: Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Location: The role is based in Cambridge and offers hybrid/remote working. Hourly Rate: £43.94phr PAYE or £58.19phr Umbrella. Role: Provide national/regional input to and execute regulatory strategies. Plan and manage local regulatory submissions in compliance with corporate standards and local regulatory requirements. Contribute to the filing plan (MA and Lifecycle maintenance), advising and discussing with the local cross-functional team and with minimal supervision, executes the filing plan (MA and Lifecycle maintenance). Collaborate with Regional and Global Study Operations (GSO) teams to support local planning and execution for clinical studies in accordance with national legal and regulatory requirements (where appropriate). Ensure local labels are developed and maintained in line with local legislation and create, review and approve source text for country labeling. Your Background: Educated to degree level or above in Life sciences or a related field. Extensive experience in Regulatory Affairs across the UK market and an understanding of the local regulatory procedures for CTAs, MAAs and all lifecycle management activities. Excellent communication skills and experience of building relationships with stakeholders to achieve results across both regional country and International borders. Strong knowledge of relevant legislation and regulations relating to medicinal products. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence
