Medical Technology Jobs

Johnson & Johnson MedTech · Dublin, Ireland

Supports intraocular lens proctoring and medical information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical use of ophthalmic products. Provides clinical guidance to healthcare professionals, generates MIR statistics reports, and collaborates with Product Safety, Marketing and R&D. Home-office based with up to 20% travel across EMEA.

Johnson & Johnson MedTech · Milan, Italy

Supports intraocular lens proctoring and medical information requests, analysing surgical cases and post-operative outcomes to optimise clinical results. Manages MIR responses within four days, produces performance statistics, and assists hospitals with sub-optimal outcomes. Home-office based with up to 20% travel, working closely with Product Safety, Marketing, R&D and Commercial teams.

Ernest Gordon Recruitment · Maidenhead · £32,000 – £35,000 pa

Carry out planned and reactive maintenance on healthcare and lifting equipment, including LOLER inspections, across a local patch from Oxford to Guildford. Work both independently and within a team, visiting hospitals, schools and care homes, with door-to-door pay and further training from senior engineers.

Sue Ross Recruitment Ltd · Sheffield · £32,000 pa

This role involves driving sales of medical devices through a consultative, virtual-first approach, combining clinical and technical expertise with strong account management. The candidate will identify customer needs, deliver product solutions, and develop strategic business plans to grow both existing and new accounts. Success requires analytical insight, proactive market awareness, and effective communication across video, phone, and in-person channels.

OrganOx · Oxford

Designs and develops electronic circuits and PCB layouts for medical devices, taking full lifecycle ownership from concept through to manufacturing handover. Work covers schematic capture, component selection, prototyping, debugging and verification against IEC 60601, collaborating closely with mechanical, software and systems engineers. Based on-site in Oxford with some remote design work.

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....

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...

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.

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.

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.

HAYS Specialist Recruitment · Oxford

Provide quality oversight across clinical activities and the Quality Management System, leading internal, external and vendor audits, managing quality events, CAPAs and root cause investigations, and supporting regulatory inspection readiness. Work cross-functionally with Clinical Operations, Pharmacovigilance, Regulatory Affairs and Quality to drive compliance across GCP, GCLP and GVP activities.