Staff Clinical Development Engineer - Incubator

Staff Clinical Development Engineer - Incubator Full-time Shift: Day Max. Salary Region 2: 268800 USD Max. Salary Region 1: 316200 USD Ways of Working: Onsite - This job is fully onsite. Employee Type: Employee Min. Salary Region 1: 219800 USD Global Job Level (HCM): Professional 5 (13) Min. Salary Region 2: 186800 USD 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. The Future Forward organization is Intuitive’s advanced concepts group. We explore emerging technologies, prototype next-generation solutions, and build software experiences that shape the future of robotic-assisted surgery. If you're ready to contribute to something bigger than yourself and help transform the future of healthcare , you'll find your purpose here. Primary Function of the Position The Staff Clinical Development Engineer - Incubator is a key member of Intuitive’s innovation incubator, reporting to the project engineering lead. In this role, you will lead the clinical development workstream for a defined opportunity, owning the design and execution of clinical de-risking activities and helping advance the program from early concept toward validated solution. Working closely with physicians and cross-functional partners, you will translate clinical and technical insights into structured development plans, drive execution of clinical and preclinical evaluations, and ensure that key risks are identified and resolved. This role operates with a high degree of independence and accountability, with responsibility for delivering the clinical evidence and workflows needed to support program advancement and investment decisions. Lead the clinical development workstream for a defined opportunity, owning clinical de-risking strategy and execution. Design and execute preclinical and early clinical evaluations to assess feasibility, usability, and performance. Develop and refine procedural workflows, use cases, and clinical approaches for the target application. Identify key technical and clinical risks and drive structured plans to resolve them. Collaborate with engineering to define and iterate on product requirements, design inputs, and performance targets. Lead clinical labs and external evaluations, ensuring rigorous execution and high-quality data generation. Translate findings into clear development direction and actionable recommendations. Partner with physicians to refine clinical strategy and ensure alignment between clinical intent and technical execution. Contribute to program advancement decisions by synthesizing evidence across clinical, technical, and user dimensions. Engage with key opinion leaders and external stakeholders to support validation and adoption readiness. Experience and Qualifications Typically 10+ years of experience in medical device development, translational R&D, or clinical engineering roles. Demonstrated experience in product development or clinical evaluation environments, including designing and executing experiments and translating results into development direction. Proven experience designing and executing clinical or preclinical evaluations and translating results into development direction. Experience working closely with clinicians and understanding clinical workflows and procedural environments. Ability to identify risks and drive structured problem-solving to resolution. Strong analytical and systems‑thinking skills, with the ability to synthesize findings into clear recommendations and next steps. Experience collaborating across engineering, clinical, and business teams to drive program milestones and outcomes. Experience with clinical labs, cadaveric or animal models, and early‑stage evaluations. Excellent communication skills, including the ability to clearly convey complex ideas across clinical and technical audiences. Exposure to Biodesign or needs‑based innovation methodologies preferred. Education and Training Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, or a related field required. Advanced degree (M.S., Ph.D., or equivalent) preferred. Working Conditions Must be available to work full‑time onsite in Sunnyvale, CA. Will require travel to clinical sites, customer locations, or conferences (up to 25%). May involve standing or walking for extended periods during clinical observations or procedures. Must be able to lift up to 20 lbs occasionally (e.g., for transporting prototypes or equipment). Ability to meet hospital credentialing and compliance requirements for clinical site access (e.g., vaccination). We are an AA/EEO/Veterans/Disabled employer. Due to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID‑19. Details can vary by role. Intuitive is an Equal Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws. U.S. Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR § 743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees who are nationals from countries currently on embargo or sanctions status. For any Intuitive role subject to export controls, final offers are contingent upon obtaining an approved export license and/or an executed TCP prior to the prospective employee’s start date, which may or may not be flexible, and within a timeframe that does not unreasonably impede the hiring need. If applicable, candidates will be notified and instructed on any requirements for these purposes. We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws. Preference will be given to qualified candidates who do not reside, or plan to reside, in Alabama, Arkansas, Delaware, Florida, Indiana, Iowa, Louisiana, Maryland, Mississippi, Missouri, Oklahoma, Pennsylvania, South Carolina, or Tennessee. This position may be filled at a different job level than listed here depending on business need and/or on the selected candidate’s experience, knowledge and skills. Compensation will be based primarily on the job level at which the role is filled and the candidate’s qualifications, consistent with applicable law. We provide market‑competitive compensation packages, inclusive of base pay, incentives, benefits, and equity. It would not be typical for someone to be hired at the top end of range for the role, as actual pay will be determined based on several factors, including experience, skills, and qualifications. The target compensation ranges are listed. #J-18808-Ljbffr Intuitive