Managing Staff Systems Analyst

IntuitiveSunnyvale, CA
Onsite

About The Position

The Advanced Product Development (APD) team leverages and advances the cutting-edge of technology to define and develop the surgical robotic systems of the future. This Managing Staff, Systems Analyst role is a senior player-coach reporting to the Vice President, Advanced Product Development in the Multiport Systems (da Vinci) business unit at Intuitive. The ideal candidate will combine deep individual technical contribution with direct people leadership of a small team of Systems Analysts who are central to the design, development, and evaluation of new products in the daVinci product line. The team is responsible for developing surgical teleoperation, motion control, and safety algorithms spanning electrical, mechanical, software, control, user interface, and safety engineering.

Requirements

  • Expert-level knowledge of control theory and its application to teleoperation, motion control, and safety-critical algorithm design.
  • Proven track record designing and implementing servo control systems for complex electro-mechanical or robotic platforms.
  • Strong embedded development skills including deep proficiency in C and modern C++; experience with real-time control systems.
  • MATLAB and Python programming capabilities, as well as hands-on hardware and software integration experience.
  • Demonstrated ability to lead or technically mentor a small group of engineers (2+ years formal leadership experience).
  • Ability to lead and influence cross-functional teams in the design of complex systems.
  • Experience with budget management, resource planning, and project/program cost tracking.
  • Comfort with design input, design output, traceability, and risk analysis in a regulated product development environment.
  • Excellent communication skills - able to convey complex technical content to cross-functional partners and organizational leadership.
  • Self-motivated and proactive; effective at leading through influence across disciplinary boundaries.

Nice To Haves

  • Medical device or safety-critical system product experience (FDA design controls, ISO 13485, ISO 14971).
  • Experience with surgical robotics, haptics, or tele-presence system design.
  • Familiarity with FPGA-based motor control or other embedded real-time architectures.
  • Ability to support, manage, and influence cross-functional teams in the design of complex robotic systems.
  • Experience developing products in a highly regulated environment with demonstrated success through FDA clearance.
  • A passion for delivering quality, innovative products that will improve millions of people’s lives — and inspiring a team to share that drive!

Responsibilities

  • Lead and mentor a team of Systems Analysts; set technical direction, assign work, track milestones, assess performance, and actively support career development.
  • Serve as technical authority for one or more major algorithmic subsystems (e.g., teleoperation, motion control, safety), drive architecture decisions, design reviews, and resolution of the hardest technical problems.
  • Apply advanced control theory to the design and verification of mechatronic and tele-robotic systems; guide the team through complex design tradeoffs.
  • Architect and implement Cartesian controls for manipulator robotics to enable precise and efficient robotic movements.
  • Lead prototype hardware planning, bring-up, and integration with existing systems; remain hands-on in the lab alongside the team.
  • Develop and oversee implementation of motion control and safety algorithms, including documentation of risks, requirements, and test protocols.
  • Lead and participate in clinical observations and experiments to ensure that performance requirements are clinically relevant and achievable.
  • Communicate system performance and team progress to the broader organization; represent the team in program-level reviews and cross-functional forums.
  • Act as the primary interface between Systems Analysis and cross-functional teams (Electrical, Mechanical, Software, Clinical, Regulatory); take ownership of issues that cross disciplinary boundaries.
  • Identify, document, and drive timely filing of intellectual property; coach the team to proactively surface and protect IP.
  • Ensure the team follows FDA design history file guidelines and holds design reviews in accordance with product development procedures.
  • Provide administrative leadership and control for planning, staffing, budgeting, and project/program cost tracking.
  • Provide engineering resources to support Manufacturing, Testing and Service to facilitate transfer of designs.
  • Support and encourage advanced innovation within the team; foster an environment that promotes creativity, risk-taking, and crisp execution.

Benefits

  • Market-competitive compensation packages, inclusive of base pay, incentives, benefits, and equity.
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