295 jobs
Johnson & Johnson MedTech Breda, Netherlands €64,000 – €103,040 pa
Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business teams, IT and suppliers. Handles study build, system integrations, release management, UAT, end-user support and training, plus automation, analytics and GenAI improvements. Hybrid role with up to 10% travel.
Johnson & Johnson MedTech Leiden, Netherlands €64,000 – €103,040 pa
Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business teams, IT and suppliers. Handles study build, release management, UAT, integrations, end-user support and audits, and drives automation, analytics and GenAI improvements. Hybrid working with up to 10% international travel.
Medtronic Eindhoven, Netherlands €106,400 – €159,600 pa
Leads portfolio governance, prioritisation and performance assessment for the Enterprise Accounts & Integrated Health Solutions portfolio, building business cases and investment recommendations. Also acts as key business stakeholder for the Market and Customer Intelligence platform, translating market and customer insights into portfolio actions and offer development. Senior individual contributor role partnering across commercial, marketing, finance and digital teams.
Wallace Hind Selection Birmingham £45,000 – £48,000 pa
Field-based new business role selling medical equipment such as stretchers, treatment chairs and examination couches into NHS and private hospitals across the West Midlands and North Wales. You build the territory from the ground up, running product demonstrations and negotiating complex multi-stakeholder procurement processes with clinical, EBME and estates teams.
Wallace Hind Selection Harlow £35,000 – £40,000 pa
Consultative field sales role promoting vascular access and oncology medical devices to NHS and private healthcare customers across the M25 region, with 80% new business generation and 20% account development. Involves working in operating room environments, preparing quotations and demonstrating equipment, plus attending fairs and congresses. Full training and mentoring is provided for entrants from graduate, clinical or B2B sales backgrounds.
Vero Hr Cambridge £45,000 – £55,000 pa
As a Quality & Regulatory Specialist, you will support clients in developing medical devices with a strong software focus, ensuring they meet regulatory requirements and quality standards. Your role involves creating and reviewing technical documentation, educating clients on regulatory needs, and collaborating with software engineers and senior stakeholders to deliver practical solutions.
Newton Colmore Cambridge
Medical Devices Consultant - Senior Mechanical Engineer - CambridgeDue to the growth of a leading Medical Devices organisation, we are currently seeking a Senior Mechanical Engineer, Project Manager, Medical Devices Inventor, or Mechanical Design Consultant for a newly approved role....
Medtronic London £76,800 – £115,200 pa
Designs and builds automated test frameworks for embedded and connected hardware used in operating rooms, covering device software, firmware integrations and hardware-software interaction rather than web or mobile apps. Works with Android AOSP, Linux edge devices and IoT gateways, validating drivers, connectivity, OTA updates and service APIs, and embedding quality gates into CI/CD pipelines alongside hardware, firmware and systems engineers.
GE HealthCare United Kingdom, YY9 9YY
Owns GE HealthCare's strategic relationships with NHS Trusts and private clinics across the North East, driving the full sales cycle for medical imaging capital equipment including CT, MR, MI, X-ray and Women's Health. Works within a matrixed organisation alongside a team of Imaging Account Managers, managing CRM forecasting, tender processes and long-term account strategy.
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.
Morgan McKinley Bampton CA$40,000 – CA$50,000 pa
Hands-on role bridging R&D and production for next-generation fluidic products, building, wiring and commissioning assembly fixtures, automated test equipment and robotic cells. Involves process scale-up (precision dispensing, laser welding, leak testing), equipment validation (FAT/SAT, IQ/OQ/PQ) and continuous improvement using root-cause analysis and SPC. Works alongside senior engineers in a fully on-site manufacturing environment.
Reed Southampton £28,000 – £35,000 pa
Hands-on warehouse role combining physical duties with stock control and systems work for a medical device manufacturer. You will manage inventory accuracy, goods receipt, picking and dispatch, and help develop SAP and WMS processes alongside the Operations Director. Distinct for its blend of floor work and administrative process improvement.
Spectrum IT Recruitment Southampton £50,000 – £60,000 pa
Hands-on role combining project delivery, commercial and financial oversight, people management and quality/regulatory compliance within a small medical-sector business. You will lead business projects, manage resources and risks, support strategic planning, monitor budgets and expenditure, and maintain compliance with medical device regulations while building customer, supplier and partner relationships.
Optical Express London £40,000 pa
Leads the internal audit programme across a regional network of clinics, conducting on-site compliance audits against HIS, CQC, HIW and RQIA standards and working with local managers on corrective action plans. Provides regulatory guidance, designs and delivers staff training, and reports compliance status to the Director of Care & Quality. Involves regular travel across the Midlands and South of England.
