Latest Medical Device Software Engineer Jobs

Senior Hardware Engineer

Design and develop complex electronic medical devices, from concept to production, with hands-on work in circuit design, PCB development, prototyping, and lab-based testing. Collaborate closely with firmware and software teams to integrate hardware into next-generation BioElectronics systems. Operate in a multidisciplinary environment with direct influence on product evolution and technology direction.

Cure Talent Dublin, City Of Dublin, Ireland £68,500 – £77,000 pa

Backend Developer

Design and develop scalable backend services, APIs, and cloud-native solutions on Microsoft Azure to support OrganOx's medical device platforms. Work with regulated software processes, build automated DevOps pipelines, and ensure secure, high-quality delivery of systems that impact clinical outcomes. Collaborate with internal and external teams to refine requirements and maintain robust technical documentation.

OrganOx Oxford, United Kingdom

On-site Permanent

Senior Software Engineer

Develop and maintain high-performance embedded software for next-generation intra-operative medical devices using modern C++ and edge computing technologies. Collaborate across multidisciplinary teams to enhance device connectivity, real-time decision support, and cloud integration within a regulated medical environment. Focus on code quality, security, and reliability in a system-critical context.

Medtronic London, United Kingdom £76,800 – £115,200 pa

Hybrid Permanent

Senior Analogue/RF Design Engineer

Design and develop analogue and RF circuits for advanced medical robotics systems, spanning concept through to verification in a regulated environment. Work within a multidisciplinary team to integrate hardware solutions and support wireless system development. Focus on innovation in surgical technology with opportunities for contract extension.

Octagon Group Livingston, West Lothian, EH54 6GS, United Kingdom £60 – £65 ph

Contract

Process Engineer

The Process Engineer will focus on improving process performance, maintaining process control, and supporting reliable manufacturing in a regulated medical device environment. Responsibilities include analysing production performance, driving improvements, and collaborating with quality and engineering teams to implement changes and optimise processes.

Michael Page Engineering & Manufacturing Cardiff, Cymru / Wales, CF10 2AF, United Kingdom £40,000 – £50,000 pa

Quality Engineer

This role involves hands-on quality engineering within a regulated medical device manufacturing environment, focusing on improving the Quality Management System (QMS) through data-driven insights and direct collaboration with production teams. The engineer will lead non-conformance investigations, support audits, drive continuous improvement initiatives, and ensure compliance with ISO 13485 and ISO 14971 standards. Emphasis is placed on practical, floor-based problem-solving to embed a quality-first culture across operations.

Aurora Life Sciences Leeds, West Yorkshire, United Kingdom £45,000 – £50,000 pa

On-site Permanent

Sr Principal Clinical Engineer

The Sr Principal Clinical Engineer acts as a Procedural Workflow Architect, defining end-to-end surgical workflows across preoperative, intraoperative, and postoperative care. This role translates clinical, usability, economic, and adoption needs into integrated procedural requirements that guide the development of implants, instruments, digital applications, and enabling technologies. The engineer collaborates with cross-functional teams to ensure solutions are intuitive, adoptable, and clinically differentiated.

Johnson & Johnson MedTech United States

On-site Permanent

Sr Principal Clinical Engineer

The role involves designing end-to-end surgical workflows across preoperative, intraoperative, and postoperative phases, translating clinical and operational needs into integrated procedural requirements. The engineer will collaborate with cross-functional teams to ensure medical solutions are intuitive, adoptable, and clinically meaningful, with a focus on innovation in orthopaedic treatments and digital surgery.

Johnson & Johnson MedTech £137,000 – £235,750 pa

Project Manager

This role involves leading the end-to-end development programme for a next-generation medical device, coordinating cross-functional teams across engineering, clinical, regulatory, and supply chain. The Project Manager will own the Integrated Development Plan, ensure compliance with ISO 13485 and FDA 510(k) requirements, manage third-party vendors, and maintain the Design History File. It is a high-visibility position central to scaling the product through regulatory submission and into commercial launch.

GxPeople Global London, United Kingdom £80,000 – £90,000 pa

Repair Centre Lead Technician

Leads a team of technicians while performing hands-on repair and maintenance of GE Healthcare's Patient Care Solutions and Ultrasound systems, diagnosing faults and ensuring quality service delivery. Manages workload, parts ordering, and service records while ensuring compliance with ISO 9001 and EHS standards. Serves as a technical and operational leader within a fast-paced medical technology environment.

GE HealthCare Hatfield, Hertfordshire, United Kingdom

Director, Regulatory Affairs, Europe

Leads the European Regulatory Affairs team at GE HealthCare, defining regulatory strategy and ensuring compliance with EU MDR and UK MDR for medical devices. Oversees CE and UKCA marking, manages interactions with Notified Bodies and Competent Authorities, and drives regulatory alignment across quality, legal, and product teams. Focuses on strategic planning, postmarket compliance, and industry engagement in a global healthcare technology environment.

GE HealthCare Chalfont St Giles, Buckinghamshire, United Kingdom

Principal Mechanical Design Engineer - Medical Devices

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...

Newton Colmore Cambridge, United Kingdom

Permanent

Ada Software Engineer

This role involves developing high-integrity, safety-critical software using Ada and SPARK across industries such as aerospace, medical devices, and nuclear systems. You'll work throughout the full software lifecycle—requirements, design, development, integration, and validation—within a rigorous, compliance-driven environment. The position emphasizes engineering precision, traceability, and adherence to standards like DO-178 and IEC 61508.

Yoh Bath, Somerset, United Kingdom £60,000 – £65,000 pa

Medical Systems Engineer

This role involves capturing and managing requirements for medical devices, ensuring compliance with regulatory standards in both hardware and software engineering. The engineer will design and implement development processes, with a focus on best coding practices and test procedures. Work is primarily remote, with occasional travel to Cheltenham.

Circuit32 Recruitment Cheltenham, Gloucestershire, United Kingdom £50 – £65 ph

Remote Contract

Rust Software Engineer

This role involves developing high-integrity, safety-critical software across industries such as aerospace, medical devices, and automotive, using Rust as the primary language. You'll work across the full software development lifecycle, including requirements, verification, and validation, in a structured, compliance-driven environment. The role emphasizes engineering rigor, traceability, and adherence to functional safety standards.

Yoh Beverley, Greater London, London, United Kingdom £60,000 – £65,000 pa