Posted 08 July, 2026
Quality Manager (Software & Informatics) Jobs in UK 2026
NewsNowGh
Auckland, AUK, NZ
Full Time
Reference: dc1bd64863cc92da
Job Description
Quality Manager (Software & Informatics)\n
\n#J-18808-LjbffrFisher & Paykel Healthcare is recruiting a Group Quality Manager for Software and Informatics operations. Although advertised for the United Kingdom, the role is based in Auckland, New Zealand. The successful candidate will receive complete immigration and relocation assistance for family members, temporary accommodation, relocation flights, extra baggage support, and rental transportation.
\nJob Duties\n- \n
- Leading software quality assurance strategies across medical technology and informatics development teams. \n
- Supporting compliance with international medical device regulations and software development standards globally. \n
- Guiding teams on Agile Development Operations within highly regulated healthcare software environments. \n
- Advising ICT leadership teams on software validation and computerized systems compliance requirements. \n
- Improving quality processes while balancing engineering excellence with agile software development practices. \n
- Driving organizational change through continuous quality improvement initiatives and strategic leadership approaches. \n
- Monitoring compliance involving Software as a Medical Device and computerized validation systems. \n
- Supporting the development of efficient quality management systems for healthcare software products. \n
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- A minimum bachelor’s degree in engineering, science, clinical studies, or related disciplines. \n
- Proven leadership experience managing engineers within software quality or medical device development environments. \n
- Strong understanding of cloud-first DevOps practices and Agile software development methodologies. \n
- Advanced knowledge of software quality standards, including ISO 13485 and IEC 62304 requirements. \n
- Experience establishing Quality Management Systems within regulated healthcare technology organizations. \n
- Familiarity with Commercial Off-the-Shelf software products and computerized validation systems. \n
- Knowledge of global medical device regulations, including EU MDR and 21 CFR 820 requirements. \n
- Excellent communication, collaboration, problem-solving, and stakeholder management abilities across diverse departments. \n