Medical Technology Jobs

TRS Consulting · St Albans · £42,000 – £45,000 pa

Servicing and repairing sophisticated medical surgical AV systems in operating theatres, NHS departments and private healthcare sites. The role combines hands-on electronic fault-finding with customer-facing troubleshooting alongside clinicians, and offers full product training for engineers from AV, medical device or ex-Forces backgrounds.

TRS Consulting · Aylesbury · £42,000 – £45,000 pa

Servicing and repairing sophisticated medical surgical AV systems in operating theatres, NHS departments and private healthcare sites. The role combines hands-on electronic fault-finding with customer-facing troubleshooting alongside clinicians, backed by full product training and a company car.

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.

SoCode · Cambridge · £40,000 – £50,000 pa

Hands-on electronics design role at a product development consultancy, owning hardware at system and circuit level from concept through prototyping, debug, verification and into production for medical and healthcare clients. Work spans medium and high-volume manufacture in well-equipped labs, with peer review across disciplines and a new technical challenge every few months.

Medtronic · London · £76,800 – £115,200 pa

Develops high-performance, low-latency video and AI processing pipelines for use in the operating room, leveraging hardware acceleration for capture, inference, visualisation and streaming. Works in a multidisciplinary team on safe-by-design medical device software, optimising real-time pipelines with C++17-23, multi-threading and inter-process communication. Requires two days per week onsite in London.

OrganOx · Oxford

Technical lead for electronics design across current and next-generation medical device products, combining hands-on design with mentoring junior engineers. Defines electronic architecture, reviews schematics and PCB layouts, and oversees verification and validation including EMC and safety testing to IEC 60601, IEC 62304 and ISO 14971 standards. Works closely with suppliers, manufacturing partners, and cross-functional quality and regulatory teams on-site in Oxford.

Medtronic · London · £76,800 – £115,200 pa

Supports software quality across the full product development lifecycle in Medtronic's surgical operating unit, from requirements and design through verification, validation, release and post-market support. Involves risk management (SFMEA, hazard analysis), design reviews, traceability documentation, CAPA and audit readiness, working closely with software, systems, regulatory and quality teams.

Kes Solutions · Houghton le Spring

Support the design, manufacture, testing and regulatory compliance of medical devices, maintaining quality control systems, production protocols and documentation. Investigate non-conformances and complaints, run CAPA, testing and validation, and assist with EU MDR, ISO 13485 and audit readiness, including clean room operations.

Newton Colmore · Cambridge

Provide regulatory support across a Cambridge product development business, guiding multidisciplinary engineering and science teams on compliance with ISO 9001, ISO 13485 and FDA 21 CFR 820. Monitor international regulatory changes, support external audits and contribute to quality management system improvements across medical and non-medical projects.

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.

Abbott Laboratories · Witney

Joins the Operations Engineering team to introduce bespoke automated production machines and own their validation strategy, from project planning and risk assessment through to delivering validated equipment into Production. Develops new validation tests, executes process equipment validations, and becomes a technical subject matter expert working with cross-functional teams and suppliers, with occasional supplier site visits.

Johnson & Johnson MedTech · Leeds

Hands-on role performing verification and investigational testing of orthopedic implants and instrumentation, developing test methods, fixtures and protocols for regulatory submissions. Works closely with R&D and Quality, contributes to design and process FMEAs, and leads departmental work instructions and audit support.

OrganOx · Oxford

Hands-on senior role designing, securing and automating Azure cloud infrastructure and CI/CD foundations for regulated medical device software and connected device services. Acts as a bridge between Digital and Data teams, supporting Databricks, SAP interfaces and enterprise data flows, with monitoring, observability and cybersecurity responsibilities. Office-based in Oxford with flexibility.

Carbometrics · Bristol · £60,000 – £70,000 pa

Lead the development of a signal-processing pipeline that turns raw optical sensor measurements into reliable analytical results, covering filtering, noise removal, bias compensation, calibration and change detection. Work hands-on with experimental data in Python, building algorithms and visualisation tools alongside scientists and engineers, with scope to grow into a team-leading role.

Johnson & Johnson MedTech · Horsham, United States · US$112,000 – US$180,550 pa

Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business, IT and suppliers. Handles study build, user support, release management, UAT, integrations and audits, while driving automation, analytics and GenAI improvements under GCP and FDA compliance.