Creating optical and electromagnetic navigation solutions for medical device OEM partners globally for over 45 years.
Waterloo, Ontario
NDI is a global authority in optical and electromagnetic (EM) navigation technology for the medical device market. Fast and accurate medical device tracking is essential to preserving optimal workflow while adding to procedure efficacy and clinician confidence. Our technology has been seamlessly integrated into numerous medical applications, including but not limited to surgical robotics, electrophysiology, neuro, spine, interventional radiology, transcranial magnetic stimulation, ENT, and orthopedics. Our optical and EM navigation solutions integrate into OEM medical devices, providing real-time instrument navigation in a broad range of applications. Backed by over 40 years of industry expertise and innovation, NDI manufactures the most accurate and responsive optical navigation solutions alongside gold standard EM navigation solutions that track sensor embedded OEM instruments without a line of sight. Navigate new possibilities with NDI, your trusted and reliable navigation technology partner.
Hybrid · Waterloo
The System Architect is responsible for designing and optimizing optical tracking systems and consumable medical devices. This includes translating user needs into technical requirements, managing architectural trade-offs, and leading technical decision-making for complex systems.
Hybrid · Waterloo
Responsible for the accurate picking, packing, and processing of customer orders to ensure on-time delivery of medical technology products. The role involves managing shipping transactions in Epicor and collaborating with cross-functional teams to maintain efficient material flow and logistics procedures.
Hybrid · Waterloo
Drive profitable growth in the surgical medical market through strategic account expansion and business development. Lead commercial performance, manage OEM partnerships, and translate market insights into product opportunities.
Hybrid · Waterloo
Lead quality engineering activities across the medical device product lifecycle to ensure compliance with global regulatory requirements. Drive design quality, lead complex investigations such as CAPAs and nonconformances, and support regulatory inspections.
