Latest UK roles, updated daily.
Leads external innovation sourcing and evaluation in Haematology, identifying preclinical to Phase 1 assets, driving due diligence, and shaping early partnering strategies. Works within the Therapeutic Area Leadership Team to advance high-potential opportunities and collaborates with Business Development to execute deals. Engages with biotech, academia, and investors to build a robust pipeline.
Leads strategic sourcing and evaluation of early-stage innovation in haematology, from preclinical to Phase 1 assets. Drives due diligence, shapes partnering strategies, and executes transactions in collaboration with Business Development. Embedded in the Therapeutic Area Leadership Team to influence portfolio planning and external innovation priorities.
This 12-month industrial placement offers hands-on experience in computational chemistry within AstraZeneca’s Oncology Medicinal Chemistry Department in Cambridge. The role involves applying machine learning, generative AI, and physics-based modelling to support drug discovery, including structure- and ligand-based design, cheminformatics workflows, and molecular dynamics simulations. The student will work alongside experienced scientists in a collaborative, innovation-driven environment at one of the world’s leading biopharma R&D centres.
This 12-month industrial placement offers a hands-on laboratory role within AstraZeneca's Oncology Bioscience team in Cambridge. You'll contribute to drug discovery research by designing and running experiments, analysing data, and supporting preclinical studies in cancer biology. The role provides mentorship, collaboration with multidisciplinary scientists, and real-world experience in a leading biopharmaceutical environment.
Lead or contribute to drug discovery programs using AI-first approaches, integrating computational chemistry with machine learning to design novel therapeutics. Guide project strategy from hit identification through candidate selection, while collaborating closely with ML scientists and cross-functional teams. Help shape and refine AI models for drug design, with opportunities to lead teams and drive innovation in a dynamic, interdisciplinary environment.
This role involves ensuring compliance with EHS, Quality, and Engineering standards in a pharmaceutical manufacturing environment. The Compliance Engineer will manage key systems including QMS, engineering standards, change control, and risk management, while supporting audits and delivering GMP training. The position drives continuous improvement and maintains documentation and governance processes within a regulated cGMP setting.
A Principal Scientist role in Translational Omics focusing on computational analysis of multi-omic data such as single-cell and spatial transcriptomics, proteomics, and metabolomics to inform drug development decisions. The role involves close collaboration with cross-functional teams to derive insights in hepatology, renal, metabolic, and cardiovascular diseases, with a strong emphasis on biomarker discovery and patient stratification. The position requires advanced expertise in statistical and machine learning methods applied to large-scale biological datasets.
The role involves end-to-end management of clinical trials within a fast-paced, AI-driven drug discovery environment. The Senior Clinical Trial Manager will lead cross-functional teams, oversee trial start-up through close-out, ensure compliance with ICH/GCP standards, and integrate AI innovations into clinical operations. Key responsibilities include vendor and budget management, clinical documentation, data oversight, and supporting regulatory readiness and audits.
The Engineering Manager (Shift) leads a multiskilled team responsible for maintaining pharmaceutical equipment and utility systems in a GMP-regulated manufacturing environment. This role involves overseeing reactive and planned maintenance, managing contractors, conducting risk assessments, and ensuring compliance with GDP, ALCOA, and GMP standards. The position operates on rotating shifts and requires strong leadership, problem-solving, and technical expertise in cleanroom operations and controlled systems.
Operate and maintain equipment in a cGMP-compliant, highly automated mRNA vaccine production environment at Moderna's Oxford facility. Perform production operations, support quality assurance, troubleshoot issues, and contribute to continuous improvement initiatives using digital systems and advanced manufacturing technologies. Work within a 2-2-3 rotating shift pattern to ensure reliable, safe, and compliant vaccine manufacturing.
Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna's Harwell site, ensuring compliance with GxP and safety standards. Establish maintenance strategies, lead capital projects, and drive continuous improvement using engineering excellence principles. Work closely with global teams and support digital integration in a high-growth biotech environment.
The Master Scheduler, Engineering is responsible for strategic planning and coordination of engineering projects, ensuring efficient resource use and adherence to timelines. This role involves leading cross-functional collaboration, monitoring project progress, mitigating risks, and ensuring compliance with regulatory standards. The position supports the delivery of innovative T cell therapies within a fast-paced biopharmaceutical environment.
Balance technical, regulatory and commercial challenges in this fulfilling roleThis highly regraded Cambridge-based medical technologies company is seeking a proven engineering leader to help guide high-value development programmes from concept through to transfer to manufacture. Your leadership will accelerate development...
This role involves joining Recursion's Internship Talent Network to be considered for future internship opportunities within a TechBio company focused on AI-driven drug discovery. Interns will engage with a platform that integrates biology, chemistry, and clinical development using proprietary AI models and large-scale automated laboratories. The position emphasizes innovation, cross-functional collaboration, and rapid learning in a mission-driven environment aimed at addressing significant unmet medical needs.
Leads global clinical evidence generation programs for diagnostic solutions, aligning scientific strategy with business goals across a matrixed organization. Oversees development of Integrated Evidence Generation Plans and manages cross-functional collaboration to ensure regulatory compliance and patient-centric outcomes. Focuses on robust clinical trial execution from inception to approval in a highly regulated international environment.
