10 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.
TTP Cambridge
Leads complex medical-device and drug-delivery development programmes from concept through to manufacture, shaping technical strategy amid significant uncertainty. Manages multidisciplinary teams, guides clients through regulatory and commercial decisions, and mentors colleagues while building new business. Based at TTP's Melbourn campus near Cambridge.
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.
SRG Darlington £49,045 – £69,045 pa
Provide senior scientific and technical leadership across complex RNA manufacturing programmes, informing technical strategy, technology selection and GMP translation. Oversee experimental studies, resolve complex challenges and work cross-functionally with technical, operations, quality, engineering and supply chain teams to deliver scalable, GMP-compatible processes.
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.
Newton Colmore Cambridge
Principal Mechanical Design Engineer - Medical Devices - CambridgeA growing Medical Devices team, based in Cambridge, is currently seeking an experienced Mechanical Design Engineer to lead the development of cutting-edge Medical Devices in the fields of Health Technology, Biotech, and...
VK Recruitment Belfast £50,000 – £65,000 pa
Oversee complex production workflows in a specialist dental laboratory, providing technical leadership across CAD/CAM, milling, 3D printing, PMMA, zirconia and ceramics. Troubleshoot equipment and software issues, improve efficiency and quality, and coach technicians and departmental leads. Reports to the Associate Director after a structured induction.
HCRG Care Group Runcorn £50,000 pa
Leads end-to-end data migration projects moving sensitive patient records between Electronic Patient Record systems, coordinating internal teams, external organisations and suppliers. Combines technical project management with data quality, information governance and clinical safety, working closely with the Head of Clinical Systems. Predominantly remote with occasional UK travel.
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.
