51 to 68 of 68 IEC 62304 Jobs in the UK

comprehensive test plans, protocols and execution reports for medical device software. V&V Leadership: Drive formal software verification and validation, ensuring adherence to IEC 62304 (Class C) and ISO 14971. Process Automation: Push test automation, CI/CD pipelines and new testing techniques forward, including LLM-assisted quality ...

shared Digital/Data needs (essential) Strong communication, stakeholder‐management, technical leadership and mentoring skills across technical and non-technical teams (essential) Experience with IEC 62304, ISO 14971, or other regulated software development and risk‐management processes (desirable) Experience with connected medical device platforms, cloud‐hosted digital health ...

software tools such as Ranorex, Playwright, Selenium, Test Complete Ability to develop source code/scripts with at least one programming language. Knowledge of IEC 62304 software lifecycle, ISO 14971 risk management, ISO 13485 quality systems and IEC 62366-1 usability engineering or comparable standards for other ...

quality, and regulatory affairs to ensure smooth execution. Alignment of development activities with industry standards and regulatory frameworks such as FDA requirements, ISO 13485, IEC 62304, CLIA, and data privacy regulations. Facilitation of Agile or hybrid delivery models tailored to the needs of regulated product development. Tracking ...

with quantitative or statistical acceptance criteria and data-driven testing. Biomedical, healthcare or digital-health experience. Experience in regulated medical technology environments. Familiarity with IEC 62304, ISO 13485 or related medical-device standards. Standard Employee Benefits Employee share option scheme 22 days' annual leave plus UK bank holidays ...

mindset and ability to work with people across the business. You’d be responsible for: Knowing the ISO standards applicable to us (13485, 14971, 62304, 82304 in particular) and understanding how they map onto day-to-day Flok activities and tools Helping us design, implement and improve processes ...

have (but we can teach you) Experience in working within a regulated SSDLC process Experience in working in MedTech, including ISO 13485 and ISO 62304 Benefits Competitive salary Share options package - all our employees have ownership in the company Private healthcare Company pension incl. salary sacrifice options 25 days ...

both clinical practice and trials. Working knowledge of computerised system validation in clinical trials, ICH E6 (GCP), GAMP 5, ISO 13485, ISO 14971, IEC 62304 and 21 CFR Part 11. Familiarity with AI-specific quality and risk frameworks: FDA AI/ML SaMD Action Plan and FDA guidance … drug development, EU AI Act, ISO/IEC 42001 and NIST AI RMF. Strong analytical and problem-solving skills, with a track record of creating low-burden processes for high-velocity product lifecycles. Technical roots in AI/ML implementation; able to engage credibly with engineers and data scientists ...

external partner work and laying the foundations for an in-house capability. You will influence architecture, ensure compliance with medical device standards such as IEC 62304, and collaborate with electronics, software, quality and regulatory teams to deliver safe, reliable products. #J-18808-Ljbffr ...

idea into something clickable that users and engineers can react to. Nice to have: Medical device experience, or exposure to ISO 13485 or IEC 62304. Software engineering or technical background. Experience with embedded or real-time software. Benefits: Company equity plan so all employees share in the success ...

PACS. You will define interoperability architecture and lead cross-functional teams in a medical device context. The role requires deep clinical software experience, IEC 62304 expertise, and hands-on leadership in delivering safe, compliant medical software across complex workflows. #J-18808-Ljbffr ...

collaboration with engineering, data science, quality and regulatory teams. Lead schedules, resourcing, risk management, and delivery roadmaps while ensuring compliance with FDA, ISO 13485, IEC 62304 and privacy rules. #J-18808-Ljbffr ...

driven development culture, gaining deep exposure to regulated medical device software development including version control, code review, automated testing, and regulatory documentation aligned with IEC 62304 standards. #J-18808-Ljbffr ...

extend coverage across tests for medical device software validations. You will mentor juniors and promote automation-first practices while aligning with ISO 13485/62304 compliance requirements. #J-18808-Ljbffr ...

against physical hardware. Desirable Experience: Robotics, manufacturing automation or surgical systems. Medical devices or other regulated industries. Safety-critical software development. ISO 13485 or IEC 62304. Test protocols, technical documentation and release management. The Opportunity: You’ll be working closely with an experienced engineering team, developing and improving applications ...

join a team building software that converts raw neuro-signals into longitudinal patient insights, contributing to the CoVision project with V&V leadership and IEC 62304 compliance. The role focuses on end-to-end SDLC testing for medical device software and internal tools, with a strong emphasis ...

Experience in a regulated industry (e.g. Banking, Medical) Experience with Data Residency requirements Knowledge of SOC2, ISO 27001 frameworks Experience with development compliant to IEC62304 Why Sava? This is a high-ownership, high-responsibility role in a company that’s building something complex, meaningful, and fast. The expectations are high ...

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 … 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 ...