4 of 4 ISO 13485 Jobs in Cambridgeshire

Engineer - Medical Devices: - Design, develop, and maintain embedded software in C for medical devices and safety‐critical systems. - Produce high‐integrity code compliant with ISO 13485 and associated medical standards. - Lead on software architecture, design reviews, and technical decision‐making. - Collaborate closely with hardware, systems, and quality teams … engineering within the medical device sector. - Strong proficiency in Embedded C and bare metal programming. - Hands‐on experience developing safety‐critical code aligned with ISO 13485. - Familiarity with structured development methodologies (e.g., V‐model, IEC 62304‐aligned processes). - Strong debugging, problem‐solving, and documentation skills. Desirable/Advantageous ...

Devices: - Design, develop, and maintain embedded software in C/C++ for medical devices and safety‐critical systems. - Produce high‐integrity code compliant with ISO 13485 and associated medical standards. - Lead on software architecture, design reviews, and technical decision‐making. - Collaborate closely with hardware, systems, and quality teams … engineering within the medical device sector. - Strong proficiency in Embedded C and bare metal programming. - Hands‐on experience developing safety‐critical code aligned with ISO 13485. - Familiarity with structured development methodologies (e.g., V‐model, IEC 62304‐aligned processes). - Strong debugging, problem‐solving, and documentation skills. Desirable/Advantageous ...

products - Lead the full hardware development lifecycle including requirements, design, prototyping, testing, debugging and production support - Ensure compliance with regulatory standards (e.g., IEC 60601, ISO 13485) - Conduct EMC testing and troubleshoot hardware issues - Collaborate with cross-functional teams to deliver integrated solutions - Maintain accurate documentation and stay current ...

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 a highly innovative ...