1 to 17 of 17 IEC 62304 Jobs

to pre-release testing. Create and maintain documentation throughout the software development process to ensure adherence to industry and medical device standards (such as IEC 62304). Responsible for reporting the latest advancements in software languages, development tools and vulnerabilities. Participate in Technical Team Innovation Days specifically focused … database management systems Programming skills in languages such as C++, Python, Java Familiarity with healthcare IT standards, HIPAA compliance, data privacy laws, and specifically IEC 62304 standards for medical software development Experience in HL7 integration A keen interest in engineering and understanding of engineering best practices and test more »

the team. Ensure that the software applications, tools and algorithms embedded in Yourgene Health CE-IVD products are developed in a manner consistent with IEC 62304 and other appropriate regulatory standards. Management of the lifecycle of Software applications, products and tools. Liaise with external software development partners as … Healthcare sector or alternatively in regulated environments in other industry sectors with a knowledge of transferrable processes. Preferably with experience of operating ISO/IEC 62304 and 62366-compliant software development processes, or to software development regulatory standards in other industry sectors. Experience of current project management and more »

ideally FreeRTOS, OPENRTOS® or SAFERTOS® Low level embedded engineering experience – ie working at processor level – Cortex M3, M4, A7 Safety Software Development to standards: IEC 61508, DO 178B/C, ISO26262, IEC 61508, IEC 62304 Networking – TCP, UDP Embedded software security Multicore devices Salary and Benefits more »

architectures. Strong C progamming/assembler/networking knowledge. It would be beneficial to have safety critical expertise with knowledge of Safety Software standards: IEC 61508, DO 178B/C, ISO26262, IEC 61508, IEC 62304 . The successful Principal Embedded Software Engineer will work alongside industry more »

attitude and strong stakeholder management skills. You should be a competent user of Microsoft Project and Trello. Knowledge of Safety Software Development to standards: IEC 61508, DO 178B/C, ISO26262, IEC 61508, IEC 62304 would be hugely beneficial but is not essential. The successful Software more »

management skills Knowledge of Safety Software Development to standards avionics, automotive, defence, medical or or safety critical standards ( eg61508, DO 178B/C, ISO26262, IEC 61508, IEC 62304) Relevant Software, electronics or IT Engineering degree. You must be based in the UK to apply for this role. more »

systems. Provide technical guidance and mentorship to junior team members, fostering a collaborative and knowledge-sharing environment. Follow the medical device software development process (IEC 62304 compliance). Who we are looking for: You have a Master's or PhD degree in Computer Sciences, Software Engineering, Biomedical Engineering more »

C#/.NET Use of circuit simulation packages Schematic capture and PCB design for small form-factor products. ISO 13485 or similar quality systems IEC 60601 family/IEC 62304 standards Previous work with medical devices Company Benefits Excellent salary Car Scheme Excellent career development. Holidays more »

in scripting (PERL, Python) and microcontroller/microprocessor tools (e.g., IAR Systems, Visual Studio). Experience with continuous integration and software testing. Knowledge of IEC 62304 standards. Familiarity with version control (JIRA, SVN), Object-Oriented programming (UML), software quality tools (PClint, Vectorcast), and build systems (Jenkins). Salary more »

fundamental elements and workflow of software development processes to predefined timescales, highly preferably in a commercial environment. Preferably with experience of operating ISO/IEC 62304-compliant software development processes. Direct experience of working with Next Generation Sequencing data sets is preferable but not essential. Enthusiasm, drive, thoroughness more »

years' experience in developing software and troubleshooting hardware issues * Previous involvement in regulated In Vitro Diagnostic (IVD) development, including operating under ISO13485 and IEC62304 * Significant experience in formal software verification * Proficiency in C/C++ programming languages * Experience with Real-Time Operating Systems and bare-metal development * Demonstrated track record more »

with the ability to work effectively with internal and external stakeholders. Familiarity with medical device regulations, standards, and best practices such as ISO 13485, IEC 62304, or FDA 21 CFR Part 11. Ability to work under pressure, meet deadlines, and deliver high-quality software products that meet customer more »

Medical Device company seeking a QA Software Engineer with 3+ years of SaMD experience with a strong knowledge of ISO 13485, ISO 60601 and IEC 62304 . The key responsibilities are as follows: • Ensure the software meets all relevant regulatory requirements • Alongside partners, prepare and maintain detailed documentation more »

and automation testing, creating test scripts and cases from scratch Experience working within a regulated environment Any Medical Device Software experience and understanding of IEC 62304 would really set your application apart! What Next? If you’re a Software Developer in Test looking to work on a meaningful more »

Job Description Join a pioneering, well-funded company at the forefront of point-of-care diagnostics as a Mid or Senior Embedded Software Engineer. Their mission is to transform the management of infectious diseases with our cutting-edge technology, working more »

Job Description Join a pioneering, well-funded company at the forefront of point-of-care diagnostics as a Embedded Software Engineer. Their mission is to transform the management of infectious diseases with our cutting-edge technology, working alongside forward-thinking more »

applications. Applying control engineering principles such as PD/PID controllers for system regulation. Engaging in coding and software lifecycle management per ISO13485, IEC6001, IEC62304, and other relevant standards. Collaborating with cross-functional teams to ensure effective product development and integration. Conducting feasibility reviews and troubleshooting to optimize software and … and ensuring timely delivery of project milestones. The experience you'll bring to the team: Essential experience and knowledge in medical devices - ISO13485, IEC6001, IEC62304, cybersecurity Proficiency in coding with C and C++ Experience with microcontroller programming, e.g. STM32 Background in control engineering, specifically with PD/PID controllers advantageous. more »