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.
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.
ACS Staffing Solutions Malvern £40,000 – £50,000 pa
Lead the Service and Repairs function for an assistive technology company, combining hands-on electronic fault diagnosis with team leadership and operational improvement. You'll coach technicians, drive root cause investigations with Hardware Engineering, and improve turnaround times and processes while preparing the department for ISO 13485 compliance. The role sits at the intersection of accessibility, technical troubleshooting and quality/regulatory work.
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.
Talentmark Airdrie £23 – £26 ph
Lead product definition for technically complex point-of-care systems, managing and coaching a team of systems and requirements engineers. Drive requirements engineering, elicitation and evaluations, and support rapid resolution of technical issues. Fully site-based in Motherwell on a 12-month contract in the medical devices sector.
Clearline Recruitment Ltd Welwyn Garden City £339 – £500 pd
Coordinate UK clinical study start-up activities and site activation, managing regulatory submissions, approvals and amendments. Liaise with NHS R&D departments, clinical sites and CROs, prepare site contracts, budgets and costing templates, and track timelines and regulatory milestones. Requires hands-on UK start-up experience with HRA, Ethics, MHRA, IRAS, CPMS and ICH-GCP knowledge.
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.
Medtronic London £95,200 – £142,800 pa
Builds and maintains the internal platform tooling that other engineering teams rely on, spanning Infrastructure as Code with OpenTofu, EKS and Helm, CI/CD automation, and observability with OpenTelemetry. Also supports AI agentic workflows and designs pragmatic fixes for developer productivity gaps, mentoring engineers across the organisation.
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.
