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Cruxx in Central New Jersey is seeking a software leader to own the navigation platform, real-time vision and registration pipeline, and AI models that underpin a surgical system.
You will inherit a small team, guide architecture from prototype to product, ensure IEC 62304 compliance, and partner with hardware, regulatory, and clinical teams to ship a device that clears regulators and serves hundreds of operating rooms.
A MedTech company, Central New Jersey. On-site. Reports to the Co-Founder and CTO.
Our client is building a complex electromechanical surgical system with vision-based, trackerless navigation: computer vision and AI that register the patient to the surgical plan to sub-millimetre accuracy in a live operating room, with no tracking hardware attached to the patient. The research works. The team recently brought registration accuracy back under half a millimetre against laser-scan ground truth. The job now is turning a research-grade system into a medical device that ships, clears regulators and runs reliably in hundreds of operating rooms.
That is a software leadership problem as much as an engineering one, and they do not yet have the person who owns it.
You will lead software engineering across the navigation platform: the real-time vision and registration pipeline, the surgical planning and intra-operative software, the integration layer that ties software to the electromechanical system, and the AI models that sit underneath. You inherit a strong, small team of software engineers, AI researchers and integration engineers who have built the core from scratch, and you grow it. Two engineers join under you in the first phase; the plan after that is a team of ten or more.
You report to a Co-Founder and CTO who came from big tech, is hands-on and in the room. He needs a partner who can run engineering day to day so he can spend more of his time on the product and the clinical problem.
Surgical and medical devices with software at the core, navigation or image-guided systems, autonomous systems, scientific instrumentation, early-stage hardware companies that shipped. A first FDA submission under your belt is a plus, not a requirement.
If you want a spec handed to you, a mature process to follow, or a team large enough to delegate everything, this is the wrong company. The pace is set by a clinical and regulatory timeline, the team is small, and the leader they hire will write code in the first ninety days.