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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Regulatory Affairs Specialist
Location: Mississauga, Ontario
Status: Full-Time
Position Summary:
The Regulatory Affairs Specialist is responsible for supporting and maintaining regulatory compliance for medical devices across global markets, including Canada, the United States, the European Union, and other regulated jurisdictions. This role prepares and manages regulatory submissions, maintains product and facility licenses and registrations, supports responses to regulatory authorities, and ensures ongoing compliance with applicable regulations and quality standards such as ISO 13485, MDSAP, EU MDR, and FDA requirements.
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Electrical Developer
Location: Mississauga, Ontario
Status: Full-Time
Position Summary:
The Electrical Engineer is responsible for the design, development, testing, and support of electrical systems and subsystems used in medical devices. Working as part of a multidisciplinary product development team, this role contributes to the design of analog, digital, and power electronics, printed circuit boards (PCBs), cable assemblies, and related electrical components from concept through commercialization.
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Systems Developer
Location: Mississauga, Ontario
Status: Full-Time
Position Summary:
The Systems Engineer is responsible for defining, developing, and verifying system and software requirements for innovative medical device products throughout the product development lifecycle. Working closely with mechanical, electrical, and software engineering teams, this role ensures products meet user needs, regulatory requirements, and performance expectations.
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Mechanical Designer
Location: Mississauga, Ontario
Status: Full-Time
Position Summary:
The Mechanical Design Engineer is responsible for the full product development lifecycle, from concept and detailed design through manufacturing transfer and product support. This role designs mechanical components and assemblies using SolidWorks, develops prototypes, creates technical documentation, and collaborates closely with cross-functional teams including manufacturing, systems engineering, quality, regulatory, and product management. The incumbent supports product development for both capital equipment and disposable components, ensuring designs are manufacturable, cost-effective, compliant with regulatory requirements, and aligned with customer needs. The role also contributes to product testing, risk assessment, intellectual property documentation, process development, and continuous improvement activities to support the successful commercialization of innovative medical technologies.
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Clinical Applications Specialist
Location: Mississauga, Ontario
Status: Full-Time
Position Summary:
Traferox is seeking a highly motivated Clinical Applications Specialist to support the adoption and successful clinical use of our organ preservation technologies. This role serves as the primary clinical resource for customers, providing education, product training, and ongoing clinical support to transplant programs.
Working closely with the Clinical Development, Commercial, Marketing, and R&D teams, the Clinical Applications Specialist will help ensure customers are confident and successful using Traferox products while also providing valuable clinical insights that support product development and commercialization efforts.
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Quality Control Associate
Location: 2400 Skymark Ave, Mississauga, ON 40121, Canada
Status: Contract
Position Summary:
The Quality Control Associate supports manufacturing operations by ensuring products, materials, and processes comply with established quality standards, regulatory requirements, and company procedures. This role is responsible for performing inspections and testing, reviewing and approving production and quality documentation, managing nonconforming materials, and supporting product release activities. The position works closely with Production, Quality Control, and Quality Assurance teams to maintain compliance with Good Manufacturing Practices (GMP), drive continuous improvement, and ensure the consistent delivery of high-quality products.
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Marketing Communications Associate
Location: Mississauga, Ontario
Status: Full-Time
Position Summary:
The Marketing Communications Associate supports the planning, development, and execution of marketing and communications initiatives that strengthen brand awareness and support commercial objectives. This role is responsible for coordinating marketing activities, developing content, managing digital channels, and ensuring the timely delivery of high-quality marketing materials across multiple platforms.
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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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