390 jobs for “Medical Device Software Engineer”
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.
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.
Vertech Group (UK) Ltd London £75,000 – £85,000 pa
Assesses software development processes and technical evidence for AI-enabled medical devices, reviewing lifecycle, V&V, configuration management and risk to determine whether safety-critical products meet certification standards. Uses AI-assisted tools to explore evidence, identify failure modes and flag inconsistencies within a specialist team.
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.
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.
Computer Futures London £75,000 – £85,000 pa
Drive software safety activities across the product lifecycle for software-based medical devices, including hazard analysis, risk assessments and safety documentation. Work with Software, Quality, Regulatory and Product Development teams to ensure compliance with standards such as ISO 14971 and IEC 62304, and support verification, validation and software risk management.
ECM Selection Cambridge £45,000 – £55,000 pa
Develop embedded C and C++ software for medical devices spanning lab and hospital equipment, drug delivery systems and personal sensors. Work across all project stages from concept through design, implementation and manufacture, with substantial client interaction. Target systems include bare metal, RTOS and Linux, with Python used for automated testing.
KO2 Embedded Recruitment Solutions Runcorn £55,000 – £65,000 pa
Senior Embedded Software EngineerLocation: Runcorn, with flexible hybrid working from homeSalary: £60,000 - £70,000 DOE, plus 8% bonusAbout the companyOur client is an innovative medical technology business. They develop critical point-of-care devices for GP surgeries, intensive care units and specialist...
OrganOx Oxford
Leads a team of Windows software engineers building device-hosted applications and services for Class II and III medical devices, covering GUI development, connectivity and cybersecurity mitigations. Owns the full SDLC, regulatory compliance (FDA, ISO 13485, IEC 62304), roadmaps, budgets and hiring, while acting as technical representative to regulators, partners and customers.
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.
ARCA Warwick
Lead medical device development projects across the full lifecycle, from concept through to manufacture, owning technical direction, budgets and timescales. Direct multidisciplinary teams spanning mechanical, electronics, software and industrial design while working with MedTech, diagnostics and life sciences clients. Combines hands-on engineering with client relationships and the commercial side of consultancy.
PDQ Engineering Recruitment & Training Services Lt Abingdon £50,000 – £55,000 pa
Leads a team of five production engineers to drive industrialisation, process improvement, and new product introduction within a regulated medical device environment. Focuses on evolving production systems through automation, Lean methodologies, and design-for-manufacture principles while ensuring quality, scalability, and regulatory compliance. Plays a central role in transitioning next-generation products from development into robust, efficient production.
Newton Colmore Cambridge
Lead cross-functional teams through the full medical device product lifecycle, from concept to commercialisation, in a multidisciplinary Cambridge environment. The role involves managing timelines and budgets, navigating regulatory pathways, and mentoring junior staff while engaging hands-on with design teams.
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.
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.
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.
