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Managing Mechanical Engineering

Job in Sunnyvale, Santa Clara County, California, 94087, USA
Listing for: Intuitive Surgical, Inc. in
Full Time position
Listed on 2026-02-28
Job specializations:
  • Engineering
    Mechanical Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Managing Staff Mechanical Engineering

Managing Staff Mechanical Engineering (Finance)

It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do  a global leader in robotic‑assisted surgery and minimally invasive care, our technologies — the da Vinci surgical system and Ion — have transformed how care is delivered for millions of patients worldwide.

We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world.

The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful — because every improvement we make has the potential to change a life.

If you're ready to contribute to something bigger than yourself and help transform the future of healthcare, you'll find your purpose here.

Job Description Managing Staff, Systems Mechanical Engineering

At Intuitive, we're transforming healthcare through innovative robotic surgical platforms that enhance patient outcomes and redefine surgical care. Our team is a passionate, cross‑functional group pioneering surgical robotics platforms. We're seeking a Managing Staff Mechanical Engineer to lead system mechanical engineering efforts for novel robotic capital equipment design in an exciting new clinical application.

Why Join Us?
  • Lead the end‑to‑end development of groundbreaking surgical robotic system hardware - from concept and prototyping through manufacturing and commercialization.
  • Collaborate closely with clinicians and interdisciplinary teams (software, electrical, controls) to deliver innovative, integrated solutions.
  • Drive technical strategy and provide hands‑on leadership in a fast‑paced, entrepreneurial environment.
  • Take part in early architecture decisions and help determine the shape of a new system and product portfolio that will reduce surgical invasiveness and improve patient outcomes worldwide.
Key Responsibilities
  • Manage and mentor a small, high‑performing team of mechanical engineers focused on robotic systems for minimally invasive surgery.
  • Operate with a "player‑coach" approach, tackling challenging technical problems yourself with creativity, rigorous engineering analysis, and an exemplary rapid design iteration process.
  • Oversee all phases of mechanical design, from prototype development to testing and through validation to ensure robust, reliable products.
  • Lead cross‑functional projects, balancing scope, schedule, budget, and risk to deliver on aggressive development goals.
  • Contribute to the identification and execution of strategies for product development, regulatory submissions, and intellectual property creation.
  • Foster a culture of innovation, quality, and continuous improvement within the team and across functions.
  • Act as a key technical resource, resolving complex design and manufacturing challenges while integrating multidisciplinary inputs.
  • Represent the team's progress and risks to senior leadership, driving transparent and proactive communication.
Qualifications What You Bring
  • Bachelor's or Master's degree in Mechanical Engineering, Mechatronics, Systems Engineering, or related discipline.
  • 5+ years' experience managing engineering teams and 7+ years designing complex mechanical products, preferably in human interface devices or robotics.
  • Deep expertise in mechanical design, materials selection, manufacturing processes, CAD modeling, and prototype development.
  • Proven experience with executing development projects in heavily regulated environments; for example, experience with FDA QSR 21 CFR Part 820, ISO 13485, IEC 60601, and other medical device regulatory standards.
  • Strong project and program management skills with a track record of delivering products on time and within budget.
  • Exceptional communication skills and ability to influence across teams and leadership levels.
  • Passion for solving challenging engineering problems and delivering patient‑impacting innovations.
Location & Commitment
  • This full‑time role is based in Sunnyvale, CA.…
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