About this role
Responsibilities:
Key Responsibilities:
● Troubleshoot and debug complex failures across actuator stacks, brakes, sensors, PCBs, power, and motion modules
● Perform root cause investigations using structured methods (5 Whys, DMAIC, Fishbone)
● Execute and refine end-of-line testing for robotic systems
● Support documentation and investigation of non-comformances
● Implement corrective actions in collaboration with design and quality teams
● Support qualification of fixtures
● Support the development and refinement of MPIs and test procedures
● Drive continuous improvements by tracking KPIs such as yield, reliability, and cycle time
● Analyze build/test data using scripting tools (eg. Python) to identify trends, anomalies and opportunities for improvement
● Assist with investigation of returned sub-assemblies/robots from the field
What you'll need:
● Bachelor’s degree in Mechatronics, Mechanical Engineering, Electrical Engineering, Manufacturing Engineering, or related field
● Minimum 1-3 years of relevant experience in manufacturing engineering, system integration or reliability engineering for complex electro-mechanical products (robotics, medical devices, or similar)
● Hands-on experience assembling, testing, or debugging electro-mechanical systems (eg. PCBs, actuators, motors, sensors)
● Ability to troubleshoot across mechanical, electrical and software interfaces
● Strong scripting and data analysis skills (Python, MATLAB, or similar)
● Experience with CAD (SolidWorks or similar) for fixture/tooling design
● Demonstrated success leading root cause investigations and implementing design/process fixes
● Strong attention to detail and comfort working in a fast-paced, hands-on environment
● Comfortable collaborating with engineers, technicians and cross-functional teams
● Excellent communication and documentation skills
● Hands-on mindset with a passion for building and improving real hardware
● Eagerness to learn and push the envelope to bring a novel surgical robotic platform to market
● Familiarity with medical device regulations (eg. ISO 13485) preferred