Principal Mechanical Engineer - Instruments

Principal Mechanical Engineer - Instruments

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 at Intuitive. As a global leader in robotic-assisted surgery and minimally invasive care, our technologies—like 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

This role may reside in Orange, CT or Sunnyvale, CA. Primary function of position: Intuitive Surgical, Inc. produces the da Vinci® Surgical System, a minimally invasive robotic surgery system that uses highly complex mechanics, replaceable instruments and accessories, and enhanced three-dimensional visualization to extend surgical technique and precision beyond the limits of the human hand. The Principal Mechanical Engineer will strive to create the safest and highest quality devices for minimally invasive surgery though rigorous and robust technical analysis. This role requires strong performance in a fast-paced, high-energy team environment and the ability to learn quickly. The ideal candidate brings deep technical expertise and hands-on experience with advanced surgical technologies to support development of surgical devices for the da Vinci Surgical.

Qualifications

Skill/Job Requirements: Bachelor's or Master's degree in Engineering, Physics, or a related field. Minimum 15 years of medical device experience. Proven experience in the development and application of medical devices, and well regarded in the industry or academia as a subject matter expert. Experience developing products compliant with safety standards and regulatory requirements for medical devices. Lead by having a breadth of technical knowledge that enables a top-level view of the entire project. Using this perspective, act as an interface between various technical specialties. Take ownership of issues that cross disciplinary boundaries to ensure the success of the project. Contribute to design documentation throughout the entire product lifecycle such as risks, specifications, test protocols, results and regulatory materials. Interested in working at a fast paced, high transaction environment providing solutions throughout the entire product lifecycle. Hands-on engineering experience with a proven ability to work well in a team environment. Proven expertise and desire to coach engineers to share knowledge and impart best practice. Ability to communicate effectively (written, oral) across all levels and organizations. Desire to learn and get to the bottom of complex and challenging engineering problems.