15 of 15 IEC 62304 Jobs in the UK

medical devices. Conduct code reviews, debugging, and optimisation with a focus on performance and power efficiency. Apply regulatory standards and software development lifecycle processes (IEC 62304, ISO 13485) throughout the project. Collaborate with hardware engineers to interpret schematics and datasheets. Produce and maintain technical documentation, including software requirements … Cortex-M microcontrollers and associated toolchains (GCC, CMake, etc.). Proficient with RTOS environments such as FreeRTOS or Zephyr. Experience working within regulated industry (IEC 62304, ISO 13485). Proficient with version control (Git) and hardware debugging tools (oscilloscopes, logic analysers). Comfortable working autonomously. Nice-to-Have ...

Proven experience as a software engineer on complex systems. Experience developing large-scale distributed systems. Significant experience in safety-critical or safety-related software (IEC 61508 preferred; IEC 62304 or IEC 26262 acceptable). Experience with Linux-based infrastructure and operating systems. Experience working in regulated ...

implications for results in development processes. Knowledge on ultrasound and/or on image data management would be appreciated. Knowledge of medical development standards (IEC 62304, ISO 14971, IEC 60601, IEC 62366) would be appreciated. You are fluent in English for technical discussion as the team ...

distributed teams Desirable: Experience with Bluetooth/BLE integrations Medical device or regulated environment experience Experience with ISO 13485 or similar QMS Knowledge of IEC 62304, ISO 13485, or other relevant standards I f you’re passionate about building high‐impact mobile applications and want to help shape ...

enabling research groups to comply with relevant safety and regulatory standards, such as of UK Medical Device Regulations (UK MRD), ISO13485, ISO 14971, and IEC 62304, by developing central resources, including Standard Operational Procedures (SOPs), templates, guidance and expert advice. The post holder will collaborate with internal teams … practical advice on safety and compliance. Applied knowledge of UK Medical Device Regulations (UK MDR) and international standards including ISO 13485, ISO 14971 and IEC 62304. Experience advising on risk management and quality assurance in software medical devices. Experience of deploying Project Management Techniques. Desirable Professional project management qualification ...

code principles to improve efficiency and scalability. Implement secure DevOps practices, including credential management and artifact signing. Support compliance standards (e.g., ISO 26262, IEC 62304) through traceable, audit-ready pipelines. In order to be successful in this role you must have: Proven experience with CI/ ...

business goals and drives innovation and competitive advantage. Regulatory Leadership : Ensure all software development activities comply with international medical device regulations and standards (e.g., IEC 62304, FDA, MDR), including risk management, documentation, and validation. Portfolio & Programme Leadership : Provide strategic leadership for the R&D software portfolio, overseeing successful ...

instruments, including middleware, firmware and algorithm development. Writing well-documented, maintainable, and test-driven code in line with medical device & industry specific standards (e.g. IEC 62304, ISO 13485, ISO 14971). Development and execution of unit, sub-system and system-level test plans. Supporting software integration with hardware ...

instruments, including middleware, firmware and algorithm development. Writing well-documented, maintainable, and test-driven code in line with medical device & industry specific standards (e.g. IEC 62304, ISO 13485, ISO 14971). Development and execution of unit, sub-system and system-level test plans. Supporting software integration with hardware ...

systems Familiarity with Qt/QML and UI frameworks (e.g., WPF, WinUI 3, UWP) Experience in regulated industries (medical, aerospace, etc.) preferred Knowledge of IEC 62304, ISO 14971, and 21 CFR Part 820 is a plus Exposure to DevOps, containers, Azure DevOps, Git, and Agile methodologies NOTICE ...

containers + Strong understanding of software development lifecycle and version control (e.g., Git). Desirable experiences for an Embedded Software Engineer: + Experience with IEC 62304, ISO 13485, or FDA 21 CFR Part 820 + 3+ years of experience in a regulated industry Apply today to join ...

knowledge communities. What Were Looking For Core Experience 5+ years of hands-on experience delivering healthcare technology solutions. Experience working with regulated SaMD products (IEC 62304 preferred). Startup or scale-up experience owning product development and growth. Strong understanding of regulated healthcare environments. Highly Desirable Knowledge ...

knowledge communities. What Were Looking For Core Experience 5+ years of hands-on experience delivering healthcare technology solutions. Experience working with regulated SaMD products (IEC 62304 preferred). Startup or scale-up experience owning product development and growth. Strong understanding of regulated healthcare environments. Highly Desirable Knowledge ...

Line management of a small team You will bring the following Hands on software engineering within medical devices with standard experience win ISO13485 and IEC62304 Prior experience as an Architect Full stack experience with IoT, cloud, web for both frontend and backend Previous track record of working across different languages ...

Python and OOP Experience with automation tools (e.g., Squish, Selenium), CI/CD, and Agile Familiarity with regulated environments and medical device standards (IEC 62304, ISO 14971) is a plus NOTICE TO THIRD PARTY AGENCIES OSI Systems, Inc. and its subsidiaries (collectively “OSI”) does not accept unsolicited resumes ...