At Traferox, we’re driven by a mission to transform transplantation—today and into the future. Join a team that’s advancing science, improving patient outcomes, and shaping the next generation of organ preservation and assessment.
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Software Developer
Location: Mississauga, Ontario
Status: Full-Time
Position Summary:
The Software Developer will design and implement software across Traferox’s product platforms, supporting product architecture development, test protocol creation and execution, and issue investigation from internal testing through customer sites. The position contributes to software release, maintenance, and optimization, and maintains the documentation required to demonstrate compliance with the company’s Quality Management System and applicable medical device regulations.
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Clinical Research Associate
Location: Mississauga, Ontario
Status: Full-Time
Position Summary:
The Clinical Research Associate will support the end-to-end execution of clinical trials and post-market activities, ensuring studies are delivered in compliance with regulatory and company standards. The position supports trial start-up, conduct, and close-out. Through proactive communication, careful planning, effective management of timelines, and documentation, the successful candidate will help drive study progress and contribute to the delivery of high-quality clinical data. The role also involves collaborating with cross-functional teams to support the development and implementation of clinical research plans. This is a full-time, in-person role based in Mississauga, ON, with travel to partnering clinical sites as needed.
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Clinical Specialist, Ex Vivo Organ Perfusion
Location: Mississauga, Ontario
Status: Full-Time
Position Summary:
The Clinical Specialist will support the clinical execution and customer education for Traferox’s ex vivo lung perfusion device across clinical sites. The position will provide in-person and virtual case support, real-time troubleshooting, and close coordination with transplant teams and Traferox’s internal clinical teams from case start through hand-off. Through structured onboarding, hands-on training, and ongoing educational content, the successful candidate will help build site readiness and maintain a high standard of device proficiency among surgeons, perfusionists, OR staff, and nursing teams. This role requires frequent travel to clinical sites in the United States and Canada (50-70%).
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Senior Regulatory Affairs Specialist
Location: Mississauga, Ontario
Status: Full-Time
Position Summary:
The Senior Regulatory Affairs Specialist supports regulatory submissions, product licensing, and compliance activities across US, EU, Canada, and other markets, including technical documentation, device registrations, complaint and adverse event reporting, audit participation, and post-market surveillance, in compliance with ISO 13485, MDSAP, and applicable regulatory requirements.
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