Latest UK roles, updated daily.
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.
The Principal Scientist role involves integrating deep expertise in computational and statistical methods to analyze large-scale genetic data, identify causal gene-phenotype links, and guide drug discovery and development. The role requires collaboration with multidisciplinary teams and staying informed about recent research in the field.
As a Data Engineer in Autonomous Systems, you will work on the AutoLabs project, building the data platform that captures, stores, and serves high-frequency multimodal data from robotic systems, sensor rigs, and lab instruments. You will collaborate with AI researchers, software engineers, and domain scientists to create a robust data layer for autonomous operations, focusing on high-throughput, low-latency ingestion and data validation.
You will design and build a full-stack AI platform that connects scientists directly to experimental results, owning the system architecture from model endpoint to user interface. The role involves rapid prototyping, close collaboration with in-house scientists, and shaping both product and technology for a novel scientific discovery platform. You'll start as an individual contributor with a path to lead technical direction.
This role involves servicing, installing, repairing, and calibrating sophisticated scientific and laboratory systems used in pharmaceutical and research environments. The position requires a background in field service engineering, particularly with high-value capital equipment and electronics.
Develops and validates ligand-binding and cell-based assays to support clinical programs for mRNA medicines. Performs pharmacodynamic and immunogenicity testing in compliance with GcLP, using platforms like Thermo Watson LIMS. Contributes to assay development, reagent management, and regulatory documentation in a fast-paced, innovative lab environment.
This role involves leading the development, qualification, and execution of complex cell-based immunoassays to support Moderna’s clinical trials across multiple therapeutic areas. The scientist will generate high-quality, regulatory-compliant data using advanced immunological techniques and serve as a subject matter expert within cross-functional teams. Emphasis is placed on innovation, scientific rigor, and integration of emerging technologies including digital and AI-enabled workflows in a GCP/GLP-regulated environment.
This role involves managing key customer accounts and driving new business by selling multi-vendor service contracts in biomedical, ultrasound, and endoscopy product lines. The candidate will identify sales opportunities, represent the company at events, and develop proposals to exceed regional targets. It is a home-based position with a focus on relationship-building and market expansion within the healthcare technology sector.
Leads global pharmacovigilance and safety strategy for gene therapy products, overseeing signal management, risk assessment, and benefit-risk profiling across investigational and marketed phases. Provides medical oversight for clinical trials, including safety data review, SAE evaluation, and regulatory submissions. Collaborates cross-functionally to ensure compliance with global safety regulations and supports health authority interactions on product safety matters.
This role involves working directly with pharmaceutical and biotechnology companies to design, build, and deploy production-grade AI solutions for complex scientific problems. Responsibilities include tailoring Owkin’s AI platform, K Pro, to client needs, translating biological questions into computational workflows, and collaborating with cross-functional teams to ensure high-quality scientific insights.
This role involves leading the Clinical Method Development and Validation team, overseeing bioanalytical method delivery, and ensuring compliance with GLP standards. Responsibilities include optimizing analytical systems, managing a team, and driving continuous improvement in a cutting-edge research environment.
This role involves servicing a wide range of biomedical devices, including high-complexity medical lasers, with ongoing training and development opportunities. The position is field-based, covering London with occasional travel and overnight stays, and emphasizes work-life balance through time off in lieu for excess hours.
The Regulatory Affairs Manager will lead day-to-day regulatory activities, maintaining and developing technical documentation for existing and future medical devices and IVD products. You'll support UKCA and CE marking, regulatory strategies, and collaborate with scientific, data, and technical teams to ensure compliance throughout product development.
This role involves managing product quality issues, leading root cause investigations, and collaborating with Engineering, Production, and Supply Chain to drive continuous improvement and defect prevention. Key responsibilities include structured problem-solving, supporting new product introductions, and monitoring quality performance measures.
The Shift Laboratory Analyst will work in a high-throughput laboratory, preparing and analysing samples, performing wet chemical and instrumental analysis, and maintaining laboratory equipment. The role involves supporting quality activities and technical projects, with a focus on accuracy and adherence to procedures.
