22 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.
Adecco Welwyn Garden City £377 – £500 ph
Coordinate early-phase clinical trials within a pharmaceutical Clinical Operations team, covering study start-up, feasibility, timelines, recruitment and vendor oversight. Maintain TMF documentation, risk logs and regulatory compliance under ICH-GCP while working with Data Management, Regulatory Affairs and external partners.
NHS Professionals Cambridge £20 – £24 ph
Undertake routine and specialist microbiological and molecular investigations across bacteriology, containment level 3, serology, chlamydia and molecular diagnostics, interpreting and reporting results. Operate and maintain automated analysers, manage consumables and use laboratory IT systems while supporting quality management, audits and SOP development. Based at Addenbrooke's Hospital within UKHSA's public health microbiology team.
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.
Adecco Surrey £200 – £300 pd
Supports a global pharmaceutical organisation's digital health strategy by identifying and evaluating early-stage opportunities that combine digital technology with healthcare products. Day to day involves market research, business case and value proposition development, external partner assessment, and Agile activities such as sprint planning and OKR reviews, working with commercial, medical, technology and brand teams.
NHS Professionals Worcestershire £20 pa
Perform biochemical analyses on patient samples using manual and automated techniques, maintain and QC point-of-care testing equipment, and authorise results for electronic reporting to wards. The role includes out-of-hours rota cover, giving technical advice to clinical staff, and supporting quality management within a hospital Clinical Biochemistry service.
University of Leeds Leeds £41,064 – £48,822 pa
Develop a clinically deployable assay for therapeutic drug monitoring of the immunosuppressant tacrolimus, building on a recently created rapid, accurate and low-cost measurement method. Work within a multidisciplinary team focused on in vitro diagnostics assays and devices that improve dosing and patient outcomes, replacing slow mass spectroscopy workflows.
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.
Clearline Recruitment Ltd Welwyn Garden City £377 – £550 pd
Operational delivery of early-phase clinical trials, coordinating multi-country study activities, timelines and site start-up while managing vendors, CROs and study documentation such as Trial Master Files. Works closely with international study teams and cross-functional groups to ensure ICH-GCP compliance, manage risks and improve study processes.
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.
Talentmark Wrexham £22 – £29 ph
Translate business requirements into user stories and acceptance criteria, working with a scrum master on story sizing and risk analysis. Participate in release and sprint planning, backlog grooming and sprint reviews, collaborating with software engineers, QA and dev-ops. Focused on clinical trial software such as EDC or eCOA within a 21 CFR Part 11 regulated environment.
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.
SoCode Cambridge £400 – £500 pd
Hands-on contract role running usability studies for advanced medical devices, covering the full study cycle from planning and moderating or observing sessions to analysing data and writing regulation-ready reports. The first project is a formative field study on cleaning and reprocessing workflows with real users, working alongside an established in-house human factors team following FDA-aligned quality procedures.
