Company Description
Apersys AG develops advanced perfusion systems that keep human organs viable and treatable for days instead of hours, enabling new possibilities in transplantation and organ rehabilitation. Its platform supports up to seven days of ex-situ preservation, allowing targeted therapeutic interventions such as defatting, metabolic support, and organ recovery. The system is automation-first, running largely unattended on a medical-grade software stack to ensure clinical practicality and safety. Apersys' technology has been featured in leading scientific publications, including a first-in-human liver transplant after three days of perfusion reported in Nature Biotechnology, and is being extended to multiple organ types. A Swiss spin-out from the Liver4Life project at Wyss Zurich, backed by ETH Zurich and the University of Zurich, Apersys is advancing toward CE marking and a US Early Feasibility Study; its devices are investigational and not yet approved for commercial use.
Role Description
The Medical Device Software Lead owns the design, development, and maintenance of the medical-grade software stack that powers Apersys' perfusion systems. This is a full-time, on-site role based in the Zürich Metropolitan Area. You'll lead a multidisciplinary software team, define architecture and technical standards, and translate clinical and research requirements into robust software solutions — staying hands-on through development, code review, and the integration of automation, monitoring, and control algorithms that keep the system reliable, safe, and compliant. You'll work closely with surgeons, biologists, engineers, and operators to support clinical studies, data acquisition, and performance improvements, while managing the software development lifecycle, coordinating with quality and regulatory teams, and driving continuous improvement in system usability and scalability.
Qualifications
- Strong background in medical device software engineering, including architecture design, embedded or real-time systems, and integration with hardware and sensors.
- Experience with safety-critical software development, IEC 62304 or related medical device standards, and quality management systems.
- Proficiency in modern programming languages (e.g., C/C++, Python, or similar), version control, CI/CD, and automated testing frameworks.
- Demonstrated ability to lead cross-functional teams, manage projects, and communicate clearly with technical and clinical stakeholders.
- Relevant degree in Computer Science, Biomedical Engineering, or a related field; an advanced degree or comparable industry experience is a plus.
- Clinical domain expertise in medicine, or exposure to translational research or medical device environments, is a plus but not required
Pay: From CHF115’470.25 per year
Benefits:
- Company pension
- Long-term profit-sharing plan
- Parental leave
Work Location: Hybrid remote in 8050 Zürich, ZH
