The Automation, Equipment and Test (AET) Team is responsible for making the robots that make the robots. We develop equipment, fixtures, and tooling that tests and calibrates our endoscope products. The engineer in this position will oversee designing and building high-precision stereo endoscope test and calibration software as part of a diverse engineering team. This position will focus on software development using C that involves controlling electro-mechanical systems (mechatronics). Our test systems have extremely high-performance standards to calibrate and test endoscopes that are safe, reliable, and consistent.
Requirements
- 8+ years of software development experience
- 5+ years of .NET (C) development experience
- Industry experience in architecture and development of scalable production software systems
- Outstanding debugging capabilities of integrated hardware/software systems
- Familiarity with physics, math, and statistics.
- Experience with cameras, image sensors, or image processing fundamentals
- Experience developing robotic or electro-mechanical systems, including control systems
Responsibilities
- Design, develop, release, deploy, and document software applications for calibration and test of endoscope vision systems from start to finish
- Control motorized stages, sensors, safety systems and other devices as part of overall test system
- Perform data analysis on manufacturing data to extract value and make data-driven decisions
- laying down the architecture and design, to leading the development, release, deployment, documentation, data analysis and sustaining of software and algorithms for test and calibration of the vision systems for Single Port da Vinci systems.
Other
- Collaborate with cross-functional teams to develop technical specifications and evaluate design trade-offs
- Write clear and concise documentation
- Strong analytical, time management, interpersonal, listening and communication skills
- Technical documentation skills for systems, software, or algorithms you develop
- Experience in medical device manufacturing or regulated engineering environment
