Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.

　　As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare's hardest challenges and advance what is possible.

　　Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere. We strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves.

　　Passionate people who want to make a difference drive our culture. Our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential.

　　Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let's advance the world of minimally invasive care.

　　Job Description The New Product Verification team at Intuitive is devoted to assuring safe, reliable, and effective products that exceed patient, surgeon, and hospital expectations. The department plays a vital role in product and process quality, in new product development and production, and in the quality of da Vinci and Ion System product lines, including diagnostic systems, instrumentation, and supporting accessories. The Senior Test Engineer will work with a cross functional team of dedicated individuals within a product development team to assure the quality of new designs, to identify issues related to new designs and processes, and to work with other Test Engineers to develop harmonized test methods.

　　Roles & Responsibilities:

　　Test Protocol Development, Execution & Reporting

　　Develops high level test plans for instrument, accessories, endoluminal, and vision projectsGenerates and takes ownership of test protocols for Design Verification and Life/ Reliability testsCollaborate with Design and Clinical teams to develop test methods needed to ensure design requirements are sufficiently verifiedExecutes test protocols for clinically-based surgical simulation and automated testing utilizing da Vinci surgical system, Ion Systems and/or other test equipmentIdentifies, reports and negotiate problems that arise during feasibility and design verification testing, and escalates new or persistent failure modes to appropriate engineering teams Test Fixture Development:

　　Designs test fixtures and other test aids needed to perform Design Verification and Life/ Reliability testsProactively identifies and develops processes and test methods that could benefit from new or updated fixture designs by engaging with design and test engineers Reasoning Ability: 

　　Ability to apply critical thinking to solve problems while leading cross-functional, technical teams in making decisions.Ability to influence technical stake holders and suggest process improvementsAbility to understand and work on complex products and processes                          Other Responsibilities

　　Ability to collaborate with cross functional teams and contribute to the development of product requirements and risk documentsEffective technical communication across various levels of the organization at core team meetings and design reviews.Ensures successful, on-time completion of department and core team projects; communicates constraints and recommends preferred mitigation to direct management when successful project completion is at riskComplies with company Department and Standard Operating ProceduresEffectively translate the functional requirements into appropriate acceptance criteria for testcases and test methods.Train test technicians on test methods and procedures Qualifications Skills, Experience, Education, & Training:

　　Education and/or Experience: 

　　Minimum of 6+ years experience working in an engineering or research team environment.Minimum BS in Mechanical, Biomedical Engineering or similar degree. MS preferred.Prefer experience within medical device or pharmaceutical industry.Medical Device Verification/Validation experience is requiredUnderstanding of design controls used in the Medical device development is required.Experience with working through various phases of medical device product development process (concept through launch) is preferred. Technical Skills: 

　　Ability to perform mechanical engineering calculations needed to support equipment design, including dimensional analysis.Experience using tools and measuring equipment (Force Gauge, Calipers, Instron, Oscilloscopes etc.).Experience with SolidWorks or similar CAD software.Experience with MATLAB, Python is highly preferred.Experience working with electro-mechanical systems is a plus.Experience in Reliability Engineering is a plus. Other skills and abilities:

　　Ability to work independently and with minimal supervision.Ability to multitask, and handle tasks with competing priorities effectively.Ability to work with biological samples, including blood, tissue and organs.Familiar with GDP skills. Integrity:

　　Accepting and adhering to high ethical, moral, and personal values in decisions, communications, actions, and when dealing with others

　　Travel:

　　Ability to travel (