Latest UK roles, updated daily.
The Principal Scientist role involves working within GSK's Genomic Technologies team to develop and apply advanced methods for analyzing large-scale genetic and genomic data. Responsibilities include collaborating with multidisciplinary teams to identify causal genes, disease mechanisms, and potential drug targets, as well as contributing to the development of best-in-class analytical tools and methodologies.
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.
Lead clinical pharmacology strategy for small molecule programs in oncology and non-oncology areas, designing and executing studies from Phase 1 through late development. Utilize AI-driven models for PK/PD prediction, dose optimization, and regulatory submissions, while managing CROs and translating preclinical data into human dosing strategies.
Lead the development and execution of nonclinical safety strategies for small molecule drug candidates in oncology and non-oncology programs, integrating AI-driven predictive models with traditional toxicology. Build and scale the nonclinical safety function within an AI-first drug discovery environment, ensuring high-quality data feedback to refine computational models. Collaborate across preclinical, clinical, and regulatory teams to advance compounds through IND and NDA/MAA-enabling studies.
Develop and lead a plant cell-based screening platform to evaluate carbon fixation and photosynthetic efficiency, using suspension cultures and genetic engineering techniques like CRISPR. Identify improved enzyme variants and metabolic pathways, then validate top candidates in whole plants to enhance crop performance. Work within a multidisciplinary team to drive discovery from lab to scalable agricultural solutions, with strong emphasis on IP generation and ethical innovation.
This role involves designing and conducting molecular biology experiments within a plant science research programme focused on improving global food production and sustainability. The scientist will work on stage-gated research milestones, contribute to intellectual property and publications, and collaborate with cross-functional teams including AI, automation, and generative biology experts. Emphasis is placed on translating scientific discoveries into scalable, real-world commercial solutions with ethical and environmental considerations.
As Lead Central Monitor, you will lead a team of Central Monitors, shaping monitoring strategies to ensure patient safety and data integrity in clinical trials. You will work across clinical, data, and risk-surveillance teams to translate complex risk signals into actionable insights and drive continuous improvement through analytics and technology.
The Central Monitor (CM) oversees and supports clinical trials through centralized monitoring activities, ensuring data quality, identifying risks, and enhancing trial oversight. They collaborate with cross-functional teams, configure Central Monitoring technology, and provide ongoing data surveillance and risk management.
This role involves hands-on maintenance and troubleshooting of GMP and non-GMP equipment in a new manufacturing facility. Responsibilities include equipment reliability, CMMS ownership, and collaboration with Engineering and QA on capital and reliability initiatives.
This role involves hands-on mRNA vaccine production operations at Moderna’s Harwell facility, adhering to cGMP standards and collaborating with Quality Assurance. Responsibilities include operating production equipment, maintaining documentation, troubleshooting issues, and contributing to continuous improvement and digital innovation.
This role involves designing and developing novel mechatronic systems for medical devices and biotechnology applications, working closely with a multidisciplinary team to take ideas from concept to manufacture. Responsibilities include creating intricate mechanisms and overseeing the overall development of complex machines.
The Product Definition Lead will guide the technical direction of complex point-of-care platforms, translating business and clinical needs into clear system requirements. You will lead a multidisciplinary team, manage requirements engineering, and support the development of medical devices and diagnostics.
Lead the development and optimisation of quantitative immunoassays for at-home diagnostic tests, from initial design through validation and commercialisation. This hands-on leadership role involves managing scientific collaborators, ensuring regulatory compliance, and translating lab-based assays into point-of-care formats such as lateral flow and microfluidic cartridges. Work with human biological samples and drive assay performance in sensitivity, precision, and stability.
This role involves providing technical leadership for software development in a medical wearable technology company, with responsibility for evolving the software architecture and ensuring compliance with IEC 62304 standards. The engineer will work across software, firmware, and signal processing domains, supporting regulatory approval and commercial launch. It is a hands-on position requiring deep expertise in regulated medical device software and systems-level engineering.
This role involves creating detailed mechanical and electro-mechanical designs for industrial machinery, focusing on improvement, modernisation, and refurbishment projects. The engineer will produce schematics, assembly drawings, BOMs, and P&IDs, ensuring compliance with UK and international standards. Work spans process machinery used in sectors like pharmaceuticals, food, and oil & gas, with some international travel required.
