Senior Test Engineer

Primary Function of Position:

The New Product Verification Department 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 robotic product lines, including diagnostic systems, endoscopic instrumentation, and supporting accessories. The Senior Test Engineer will work with a 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 projects

• Generates and takes ownership of test protocols for Design Verification and Life/ Reliability tests

• Develops clinically relevant test methods ensure design requirements are sufficiently verified by collaborating with appropriate cross functional partners

• Executes test protocols for clinically-based surgical simulation and automated testing utilizing da Vinci surgical system, Ion Systems and/or other test equipment

• Identifies, reports and negotiate problems that arise during feasibility and design verification testing, and escalates new or persistent failure modes to appropriate engineering teams

• Proactively engages with appropriate engineering teams and leads failure investigation and root cause analysis

• Clearly documents test results and observations in test report.

Test Fixture Development:

• Designs test fixtures and other test aids needed to perform Design Verification and Life/ Reliability tests

• Proactively 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 improvements

• Ability 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 documents

• Effective 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 risk

• Complies with company Department and Standard Operating Procedures

• Effectively translate the functional requirements into appropriate acceptance criteria for testcases and test methods.

• Train test technicians on test methods and procedures

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 required

• Understanding 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, Arduino is highly preferred.

• Experience working with electro-mechanical systems is a plus.

• Experience with Test Method Validation is highly preferred.

• 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:

Role is set schedule and based in Sunnyvale, California. Ability to travel (10%) as needed to support programs at other facilities

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.

Mandatory Notices

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.

Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government’s licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan (“TCP”) (note: typically adds 2 weeks to the hiring process).

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.