Director, Hardware Lifecycle Engineering

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.  We provide an inclusive work environment where each person is considered as an individual.  At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Technology Product & Platform Management

Job Sub Function:

Reliability Engineering

Job Category:

People Leader

All Job Posting Locations:

Santa Clara, California, United States of America

Job Description:

The Robotics and Digital solutions (RAD) group, part of the Johnson & Johnson family of companies, is recruiting for a Director, Hardware Lifecycle Engineering for the Robotics and Digital R&D Team. This position is located in Santa Clara, CA.

What We Do:

At Johnson & Johnson MedTech, we are building the future of robotic surgery and healthcare through innovation and technical excellence. Our goal is to develop advanced robotic platforms that are precise, reliable, and accessible. Our team focuses on creating solutions that empower surgeons and improve patient outcomes worldwide.

Who We Are:

Within RAD R&D we are a team of clinical, electrical, firmware, mechanical, mechatronics, robotic controls, systems and software engineers who are passionate about improving patient care. The team includes a wide range of experience levels from junior engineers to industry experts. We follow an iterative, collaborative approach to product development, working across clinical, instrument, accessories, and system teams. We prioritize autonomy, foster a culture of learning, and value diversity of thought and background. Our environment is inclusive, supportive, and driven by a shared commitment to innovation and excellence in healthcare.

You:

As a leader in our team, you will join us in our journey to design and deliver some of the most advanced medical robotic systems in the world. You will work closely with multi-functional teams to influence technical strategies, guide the development process, and deliver tangible results. This role offers significant leadership responsibility, growth opportunities, and the chance to have a significant impact on global healthcare.

Performance Objectives and Responsibilities:

• Lead a focused team of reliability, electrical, and mechanical engineers responsible for the testing, characterization, and design improvements of robotic hardware systems.

• Define and execute a multi-year hardware reliability strategy aligned to product roadmap, clinical requirements, and commercial goals.

• Build, lead, and develop high-performing reliability, test, and failure-analysis teams.

• Drive day-to-day execution of robotic hardware reliability projects for the Ottava program, balancing scope, schedule, and budget.

• Define system-level reliability targets and verification/validation plans that reflect clinical usage and OR workflows.

• Ensure hardware testing and development meets regulatory and quality standards, maintaining accurate and compliant documentation throughout.

• Contribute to innovation efforts by supporting prototyping new concepts, investigating emerging technologies, and implementing design improvements.

Qualifications

Required Knowledge/Skills, Education, And Experience:

• Background in Electrical, Mechanical, or related engineering fields.

• 10+ years of R&D experience in designing and developing complex hardware for electro-mechanical systems, with at least 5+ years focused on hardware reliability.

• Demonstrated success in leading engineering teams through concept, design, build, and verification phases.

• Solid understanding of medical device regulations (e.g., IEC60601, IEC61010, 21CFR820, ISO13485).

• Skilled collaborator who can work effectively w