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.
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.
Real Glasgow £60 – £75 ph
Design, develop and test electronic systems and components, covering circuit design, schematic capture, PCB layout, troubleshooting, design reviews and project documentation. Works with cross-functional teams on robust, compliant solutions, with analogue, power supply, EMC and Altium skills; medical devices experience is desirable.
SoCode Cambridge £50 – £65 ph
Embedded contractor role within an established medical technology company's electronics team, supporting complex designs from requirements and schematic capture through design reviews, PCBA layout, board bring-up and system test. Requires broad electronics design experience with depth in areas such as embedded microprocessors, motor drives, FPGA, analogue sensors or high-speed communications, using Altium Designer and DFx/EMC principles.
Clearline Recruitment Ltd Welwyn Garden City £38 – £56 ph
Independently manages end-to-end clinical data management across one or more studies, from CRF and database design through to final study closure. Works closely with Biostatistics, Data Science and Clinical Operations, overseeing data vendors and resolving complex issues across EDC, ePRO and IRT systems. Requires strong knowledge of CDISC standards and risk-based monitoring.
Reed Technology Cambridge £85,000 – £100,000 pa
Lead information security, product cybersecurity and cyber risk management for a digital health organisation, owning the ISMS, policies and controls. Day to day involves risk assessments, threat modelling, penetration testing oversight, cloud and application security, incident response and supporting audits and regulatory submissions. Works closely with software development, quality, regulatory and clinical teams, acting as the security subject matter expert.
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.
Carbon 60 London £50 – £65 ph
Analyses post-market complaints and quality data for a global medical device portfolio, leading monthly product quality monitoring and statistical trending to surface emerging risks. Builds and maintains Power BI dashboards and reporting tools, conducts complaint investigations and ad hoc reviews, and supports EU MDR trending, audits and CAPA activities alongside Quality, Regulatory, Clinical, R&D and Operations teams.
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.
Talentmark Stirling £25 – £27 ph
Execute complex experimental workstreams from concept through to design transfer, analysing multi-factorial data and presenting technical findings to stakeholders. Apply Design for Manufacture principles to optimise product formulations and characterisation, while upholding GLP, GMP and GDP compliance in a fully site-based laboratory. Requires diagnostic immunoassay expertise, ideally with particle-based assays and fluorescent detection.
Talentmark Welwyn Garden City £38 – £60 ph
Independently manage end-to-end clinical data management for one or more studies, from CRF and database design through to final study closure. Collaborate with Biostats, Data Science and Clinical teams to define data specifications, resolve complex data issues using risk-based monitoring, and oversee third-party vendors to meet regulatory and quality expectations.
