11 jobs
Bluetree Cambridge £65,000 – £80,000 pa
Lead regulatory strategy for a cardiology device company expanding into the US, UK, EU and Middle East, owning FDA, CE and UKCA submissions from Class I to Class II/III. Drive an audit-ready QMS (ISO 13485, 21 CFR Part 820, ISO 14971) and advise senior leadership on regulation, quality and clinical governance, working directly with the FDA, MHRA and notified bodies.
Johnson & Johnson MedTech Maidenhead
Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. You will design reproducible experiments, prototype layered safeguards, publish results, and work with platform engineers to move validated methods into a GenAI platform.
Johnson & Johnson MedTech Limerick, Ireland
Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance and safety-native architecture. Hands-on work prototyping and validating methods on real GenAI platform workflows, publishing results and handing validated approaches to engineering partners.
SPD Development Company Ltd Bedford £30,000 – £35,000 pa
Supports the conduct and monitoring of clinical studies, covering study set-up, sourcing and shipping supplies, volunteer recruitment, tracking study status, administering volunteer payments and maintaining inspection-ready documentation. Works within a clinical programme under GCP, with exposure to IVDR and ISO standards, in a 12-month fixed term contract.
A259 Recruitment Wick £13 ph
Assemble small plastic components for medical and non-medical devices at a client site in Littlehampton, working on a production line with full training and uniform provided. Shifts cover day, twilight or night patterns across Monday to Friday, with the role starting as temporary and transitioning to permanent after 12 consecutive weeks.
Ritz Recruitment London £14 ph
Support a busy pathology laboratory by registering patient details, receiving and preparing samples, and processing specimens for diagnostic testing. Handle enquiries from healthcare professionals, dispatch samples under biohazard rules, manage stock and waste, and keep work areas clean. Requires a biomedical science degree and prior sample reception experience.
Entrust Resource Solutions Livingston £13 ph
Packing products in a quality-focused medical device manufacturing environment, following Standard Operating Procedures and completing batch records and production paperwork accurately. The role involves identifying and reporting quality concerns or equipment faults, maintaining a clean and safe work area, and adhering to GMP, health and safety and gowning requirements. It suits someone with strong attention to detail who is comfortable with routine tasks and team working.
University of Oxford Oxford £39,424 – £47,779 pa
Develops cutting-edge machine learning and computer vision methods to analyse multi-omic and biomedical imaging data, identifying disease phenotypes and tissue architecture changes. Works with software engineers and data platform developers to translate research prototypes into robust, reproducible tools, bridging research and implementation.
University of Glasgow Glasgow £33,951 – £37,694 pa
Develops a stabilisation fluid added to cerebrospinal fluid samples to preserve leukaemia cells for flow cytometry analysis, optimising the formulation and validating it with patient samples. The role also involves contributing to research publications and proposals and helping manage the project within a university research group.
University of Birmingham Birmingham
Fully funded PhD studentship in Chemical and Biomedical Engineering, joining the Advanced Nano Materials, Structures and Applications group. The research develops miniaturised point-of-care diagnostic devices, engineering intelligent spectroscopic techniques to non-invasively detect and quantify disease, with clinical validation and applications in monitoring cellular and tissue responses to therapy.
Johnson & Johnson MedTech Beerse, Belgium
Lead a two-year postdoctoral research program on making agentic AI safe for regulated pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. You will design reproducible experiments, prototype layered architectures, and work with platform engineers to move validated methods into a GenAI platform. The role is hands-on research with real systems as the testbed, not frontier model pre-training or production engineering.
Johnson & Johnson MedTech Leiden, Netherlands
Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, continuous adversarial red-teaming, and safety-native architecture. Hands-on work prototyping and validating methods on real GenAI platform workflows, publishing results, and transitioning validated approaches into production with engineering partners.
