Manager Robotic Algorithms & Controls
| Company | Intuitive Surgical |
|---|---|
| Location | Sunnyvale, CA, USA |
| Salary | $Not Provided – $Not Provided |
| Type | Full-Time |
| Degrees | Master’s, PhD |
| Experience Level | Senior |
Requirements
- Minimum Masters in robotics related engineering field, with 6 years of experience in control of mechatronic systems, or Ph.D. with 3 years of experience in control of mechatronic systems.
- Minimum 1-3 years of people management experience, or 3-5 years of cross-functional technical leadership in a Robotic Algorithms and Controls Engineers or equivalent role.
- Familiarity with design control processes. Prior experience in product development under medical device standards (such as ISO 13485, IEC 60601, and IEC 62304), is a plus.
- Exceptional embedded C/C++ programming capabilities as well as electromechanical and software integration skills.
- Understanding of, and experience in, implementing classical and modern servo control systems.
- Exceptional engineering intuition for mechatronic systems, combined with a detailed and data-oriented approach to developing and pushing designs to completion.
- Excellent communication skills, both written and verbal, to facilitate robust conclusions.
- Passion for product quality and continuous improvements across multiple functions.
Responsibilities
- Manage and support a team of Robotic Algorithms & Controls Engineers towards successful accomplishment of product implementation with best-in-class solutions and architectures
- Provide in-depth analysis and characterization of electromechanical architectures during the entire design life cycle.
- Facilitate mechanical, electrical, and software integration of new prototypes and new products including complete robotic systems, manipulators, instruments, accessories, and endoscopes
- Analyze complex electro-mechanical devices for dynamic safety and clinical risk
- Implement safety monitoring algorithms based on sound physics and risk analysis
- Participate in clinical observations and experiments to ensure that performance requirements are relevant and realistic
- Adhere to, and contribute to, design control processes, including design review presentations, design documentation, and verification & validation testing activities
- Support the definition of manufacturing specifications and the ability to confirm devices meet those specifications
- Document and pursue intellectual property
- Communicate system architectural choices to the cross functional engineering team
- Improve cross functional workflow and interaction through tool building and teaching others
Preferred Qualifications
- Prior experience in product development under medical device standards (such as ISO 13485, IEC 60601, and IEC 62304), is a plus.