Latest UK roles, updated daily.
The VP, Medicine Development Leader for Cancer Vaccines will lead the global development of GSK's cancer vaccine, from early stages through approval and launch. This role involves strategic planning, team leadership, and collaboration with various stakeholders across R&D and commercial functions to ensure the successful development and commercialization of the vaccine.
This role involves developing and executing the analytical network strategy for GSK's supply chain, ensuring alignment with quality objectives. Responsibilities include defining QC testing principles, driving innovation in QC testing, and collaborating with cross-functional teams to integrate analytical testing into the end-to-end supply chain process.
This role involves designing and conducting experiments in advanced genome technologies and next-generation plant transformation to enhance plant engineering capabilities. The scientist will work on genetic manipulation, DNA/RNA delivery, and plant regeneration, contributing to high-impact research with real-world applications in food security and sustainable agriculture. Collaboration with AI, automation, and generative biology experts across EIT’s ecosystem is a key part of the role.
This role involves developing metabolic engineering and synthetic biology strategies to optimise plant respiratory activity, energy status, and redox balance. Work is conducted in plant cell cultures and whole plants using iterative design–build–test–learn cycles, with translation from lab to real-world applications supported by multi-omics phenotyping and cross-disciplinary collaboration. The scientist will drive IP generation and contribute to commercialising innovations in sustainable agriculture and plant-based production.
This role involves leading early-phase clinical development (Phase 1 and 2) of novel gastroenterology therapies, with a focus on inflammatory bowel disease (IBD). The Translational Medicine Expert will design clinical development plans, serve as medical lead for trials, and collaborate closely with research, biomarker, and late-phase development teams. The position requires strong scientific leadership, engagement with key opinion leaders, and active involvement in regulatory interactions.
Lead a global team of statistical programmers, driving standardization, innovation, and quality in clinical trial data analysis. Develop programming strategies using modern tools like R, Git, and AI-enabled technologies, ensuring audit-ready deliverables and alignment with biostatistics and data management. Provide technical leadership and influence global drug development strategy across phases I–IV studies.
This role involves leading CMC regulatory strategies for international submissions, including IND/CTA/BLA/MAA filings, with a focus on mRNA-based medicines. The individual will guide global regulatory compliance, interact with health authorities, and support quality and manufacturing teams across therapeutic areas like vaccines, oncology, and rare diseases. It requires deep expertise in biologics CMC regulations and a proactive approach to navigating complex regulatory landscapes.
Lead the development and execution of CMC regulatory strategies for mRNA-based products across global submissions, including IND/CTA/BLA/MAA filings. Provide expert guidance on regulatory compliance, interact with health authorities, and support quality and manufacturing teams through change controls and submissions. Work within a multidisciplinary team at the Harwell site to advance Moderna’s pipeline in vaccines, oncology, and rare diseases.
This role involves servicing, installing, repairing, and calibrating sophisticated medical laboratory automation systems across Europe. You will work with a variety of scientific products in pathology departments, research labs, and pharmaceutical environments, requiring extensive travel and overnight stays.
This role involves servicing, installing, repairing, and calibrating sophisticated medical laboratory automation systems across Europe. You will support scientific products in various settings, including pathology departments, university research labs, and pharmaceutical environments, with extensive travel and frequent overnight stays.
This role involves working in Pfizer's Regulatory Strategy department, contributing to the development and implementation of regulatory strategies for innovative medicinal products. Responsibilities include compiling regulatory documents, engaging with health authorities, and maintaining systems and processes. The position offers a unique overview of the pharmaceutical product life cycle from research to market.
This role involves conducting incoming and dimensional inspections of components, materials, and finished goods in a meditech environment. Responsibilities include completing FAI reports, using measuring equipment, and maintaining quality records, with a focus on precision and compliance with QMS standards.
The Product Definition Lead will drive the technical direction and product definition for complex medical device systems, manage a team of systems and requirements engineers, and support the engineering team with technical issue resolution. The role involves close collaboration with interdisciplinary teams to translate business and clinical needs into precise requirements.
The Information Security Manager will lead information security, product cybersecurity, and cyber risk management in a growing, highly regulated digital health technology environment. Key responsibilities include maintaining the ISMS, conducting risk assessments, overseeing penetration testing, and embedding cybersecurity in software development processes.
The Compliance Engineer will be responsible for creating, reviewing, and maintaining regulatory and technical documentation to ensure products remain compliant and audit-ready. Key responsibilities include authoring technical files, supporting EU MDR and UK regulatory compliance, and assisting with Notified Body and external audit requirements.
