critical systems, such as aerospace, automotive, or medical devices. Familiarity with software testing, static analysis, or compliance tools. Knowledge of industry standards such as ISO 26262, DO-178C, or IEC 62304. Ability to speak a second language is a plus. Why Join Represent a highly respected suite of solutions used by leading organizations worldwide to improve software quality and More ❯
and maintain robust Python applications for medical device software Collaborate with cross-functional teams, including R&D, product management, and QA Ensure software meets regulatory standards (e.g., ISO 13485, IEC62304) for medical devices Write clean, efficient, and well-documented code following best practices Participate in code reviews, testing, and continuous improvement initiatives Requirements: Strong experience in Python More ❯
and maintain robust Python applications for medical device software. Collaborate with cross-functional teams, including R&D, product management, and QA. Ensure software meets regulatory standards (e.g., ISO 13485, IEC62304) for medical devices. Write clean, efficient, and well-documented code following best practices. Participate in code reviews, testing, and continuous improvement initiatives. Requirements Strong experience in Python More ❯
Develop robust and efficient algorithms for real-time data analysis and image processing Contribute to algorithm performance testing design and implementation Implement SaMD design control process in alignment with IEC62304's software lifecycle processes Qualifications Required: Degree in Computer Science, Biomedical Engineering, or related field Experience with real-time processing systems Experience in AI/ML or More ❯
London, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
skills and demonstrable experience in test automation (preferably Python and Kotlin). Experience with virtualization, Linux, and remote device management. Knowledge of medical device regulations and standards (ISO 13485, IEC62304, 21 CFR 820). Nice to Haves: BS/MS in Computer, Electrical, Electronics Engineering or equivalent industry experience. Advanced certification in software testing and modern quality More ❯
detection). Proficient in Python and ML frameworks such as PyTorch or TensorFlow. Familiarity with FDA regulatory pathways for medical software (e.g., 510(k), De Novo), and standards like IEC62304 or ISO 13485. Experience with MLOps practices and model versioning in compliant environments. Preferred Qualifications: Experience building ML models with wearable data (e.g., continuous heart rate, motion More ❯
detection). Proficient in Python and ML frameworks such as PyTorch or TensorFlow. Familiarity with FDA regulatory pathways for medical software (e.g., 510(k), De Novo), and standards like IEC62304 or ISO 13485. Experience with MLOps practices and model versioning in compliant environments. Preferred Qualifications: Experience building ML models with wearable data (e.g., continuous heart rate, motion More ❯
CD pipelines (GitLab preferred) Strong communication skills and experience working in agile teams Understanding of AI as a Medical Device (AIaMD) development and relevant regulations (EU MDR, FDA, ISO 62304, ISO 14971, ISO 34971) Comfortable working with Linux-based systems Experience with Django Knowledge of SQL and database schema design Exposure to Next.js/TypeScript (beneficial but not essential More ❯
in signal processing and time-series modelling. Proficiency in Python and ML frameworks such as PyTorch or TensorFlow. Familiarity with FDA regulatory pathways for medical software and standards like IEC62304 or ISO 13485. Experience with MLOps practices and model versioning in compliant environments. Robert Walters Operations Limited is an employment business and employment agency and welcomes applications More ❯
performance metrics alongside error diagnostics. Preferred Experience in a regulated industry (e.g. Banking, Medical) Experience with Data Residency requirements Experience with SOC2, ISO 27001 Experience with development compliant to IEC62304 About us All the health information we need is within us. Just below the skin. SAVA is redefining the way people interact with their health by developing the most advanced More ❯
experience in medical device Quality Management Systems and regulatory processes including ISO 13485, ISO 14971, ISO 27001, 21 CFR Part 11, 21 CFR Part 820, MDR 2017/745, IEC 62304. Proven track record in interactions with Notified Bodies and/or Regulatory Authorities, especially the FDA. Knowledge of UK, US and/or EU Data Protection Regulations (i.e. More ❯
Guildford, England, United Kingdom Hybrid / WFH Options
Hypersonic Laboratories
England, United Kingdom 1 week ago BUILDING SERVICES - Junior Mechanical Project Manager Winnersh, England, United Kingdom 3 months ago Remote Senior Risk Management Engineer, Medical Devices (ISO 14971/IEC 60601/IEC62304) 12 months Fixed Term contract bei Vision RT Surrey, England, United Kingdom 1 month ago We’re unlocking community knowledge in a new More ❯
London, England, United Kingdom Hybrid / WFH Options
Acurable
understand requirements to work on new and exciting features. Define, document and implement comprehensive unit and functional tests for each one of the app components. Write code following the IEC62304 based software development lifecycle. Challenge yourself and others, learn new technologies, and have fun! What you should bring to Acurable Bachelor’s or Master’s degree in Engineering, Computer Science More ❯