Product Development Engineering Spring Co-op
Johnson & Johnson
- Location
- Santa Clara, California, United States of America
- Employment
- Internship
- Work model
- On-Site
- Level
- Intern
- H-1B history
- 2 approvals (FY2023)
- Posted
- Sep 9, 2026
Skills
About this role
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: Career Programs Job Sub Function: Non-LDP Intern/Co-Op Job Category: Career Program All Job Posting Locations: Santa Clara, California, United States of America Job Description: About MedTech Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech Position Summary We are seeking a motivated Product Development Engineering Intern to support the OTTAVA Surgical Robotic Platform within the Development Engineering organization. The intern will work alongside experienced engineers, technical specialists, manufacturing partners, quality teams, and suppliers to support New Product Development (NPD), New Product Introduction (NPI), design transfer, component development, manufacturing readiness, and continuous improvement activities. This role provides hands-on exposure to regulated medical device development, design for manufacturability, engineering analysis, supplier collaboration, and cross-functional problem solving.
Responsibilities
Assist internal teams and external suppliers with planning, development, qualification, and stabilization of components, equipment, and manufacturing processes for NPD and NPI projects. Support cross-functional collaboration with R&D, Manufacturing, Quality, Product Management, and suppliers to evaluate design options and manufacturing solutions. Apply Design for Manufacturing, Design for Assembly, and Design-to-Cost principles to help assess manufacturability, assembly flow, cost tradeoffs, and design robustness. Assist with tolerance stack-up, GD&T review, basic engineering analysis, and documentation to support robust and manufacturable component designs. Support design reviews by preparing technical inputs, documenting risks, capturing action items, and helping evaluate feasibility, manufacturability, and cost considerations. Participate in design transfer activities to support a smooth and compliant transition from development into manufacturing. Support engineering builds, pilot runs, troubleshooting activities, root cause investigations, and corrective action follow-up. Assist with PFMEA inputs, process characterization, control strategies, measurement system analysis, and statistical review under engineering guidance. Help manage project documentation, engineering deliverables, design change inputs, and build readiness materials to minimize impact to assembly and manufacturing processes. Preferred Projects Component design support, design updates, and manufacturability assessments Tolerance stack-up, GD&T review, and basic engineering analysis support Design for Manufacturing and Design for Assembly improvement projects Cost engineering and design simplification support activities Engineering build readiness, pilot run support, and issue tracking Process characterization, PFMEA support, and control plan documentation Supplier engineering support for component development, qualification, and technical follow-up Qualifications Required