Product Development Engineering Spring Co-op

6267-Auris Health Inc. Legal Entity; Santa Clara (CA); On-site; USD 37,000 - 84,000; Full time

Benefits offered by this job

Medical benefits

Sick time benefits

Retirement plan

Job summary

Johnson & Johnson in Santa Clara seeks a Product Development Engineering Intern to support the OTTAVA Surgical Robotic Platform within Development Engineering. You will work with engineers, suppliers, and quality teams on NPD, NPI, design transfer, and manufacturing readiness, gaining hands-on exposure to regulated medical device development.

Preferred projects include DFM/DFM, GD&T, tolerance analysis, and cross‑functional problem solving.

Qualifications

• Pursuing a Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Mechatronics, Manufacturing Engineering, or related engineering discipline.
• Foundational understanding of design principles for mechanical/electro-mechanical products.
• Basic knowledge of 3D CAD tools such as SolidWorks, Creo, or equivalents.
• Exposure to GD&T, engineering drawings, tolerance analysis, ASME Y14.5 concepts.
• Interest in DF(M)/DF(A), cost engineering, and scalable manufacturing process development.
• Strong analytical, problem-solving, documentation, and communication skills.
• Ability to work independently and in cross-functional teams.

Responsibilities

• Assist with planning, development, qualification, and stabilization of components and processes for NPD/NPI.
• Collaborate with R&D, Manufacturing, Quality, Product Management and suppliers.
• Apply DFM/DFM principles to assess manufacturability, assembly flow, and cost.
• Support tolerance stack‑up, GD&T review, basic engineering analysis, and documentation.
• Help with design reviews, risks, action items, and feasibility/cost considerations.
• Participate in design transfer activities to support manufacturing readiness.
• Support builds, pilot runs, troubleshooting, root-cause analysis, and CAPA follow-up.
• Assist with PFMEA inputs, process characterization, control strategies, and SQA tools.

Skills

Mechanical, electro-mechanical

Opto-mechanical understanding

Product design principles

DFM and DFA awareness

Analytical problem solving

Technical communication

Education

Bachelor’s or Master’s in Engineering

Tools

3D CAD (SolidWorks/Creo)

Job description

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

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

• Pursuing a Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Mechatronics, Manufacturing Engineering, or a related engineering discipline.
• Foundational understanding of mechanical, electro‑mechanical, opto‑mechanical, or related product and component design principles.
• Basic knowledge of 3D CAD tools such as SolidWorks, Creo, or equivalent engineering design software.
• Exposure to GD&T, engineering drawings, tolerance analysis, or ASME Y14.5 concepts.
• Interest in Design for Manufacturing, Design for Assembly, cost engineering, and scalable manufacturing process development.
• Strong analytical, problem‑solving, documentation, and technical communication skills.
• Ability to work independently while collaborating effectively in a cross‑functional team environment.

Preferred Coursework, project experience, or internship exposure related to medical devices, robotics, manufacturing, product development, or regulated engineering environments.

Experience designing, building, testing, or troubleshooting mechanical, electro‑mechanical, fiber, laser, or automated equipment systems.

Familiarity with manufacturing processes such as injection molding, machining, joining, laser welding, riveting, soldering, pressing, extrusion, overmolding, coating, or assembly methods.

Exposure to measurement systems analysis, GR&R, DOE, process capability, process stability, or statistical analysis tools.

Familiarity with medical device quality systems, design controls, ISO 13485, ISO 14971, 21 CFR 820, GMP, or related standards.

Interest in test method development, test method validation, equipment qualification, IQ/OQ/PQ, or manufacturing process validation.

Process excellence, Lean, Six Sigma, or continuous improvement coursework or project experience.

What the Intern Will Learn

• How Product Development Engineering supports NPD, NPI, design transfer, and manufacturing readiness for a surgical robotics platform.
• How cross‑functional engineering teams translate design requirements into manufacturable, scalable, and quality‑compliant solutions.
• Practical application of DFM, DFA, Design‑to‑Cost, tolerance analysis, GD&T, engineering documentation, and structured design reviews.
• How engineering builds, pilot runs, root cause analysis, process characterization, PFMEA, and control strategies support product development and production readiness.
• How supplier collaboration, component qualification, technical communication, and design change control are managed within a regulated medical device environment.
• How development engineering decisions connect to patient impact, quality, regulatory compliance, cost, manufacturability, and business objectives.

Permanently authorized to work in the U.S., must not require sponsorship of an employment visa (e.g., H‑1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually requires future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long‑term status that does not require company sponsorship.

The expected pay range for this position is between $27.00 per hour and $61.00 per hour but will be based on candidate's program year, discipline, degree and/or experience.

Co‑Ops/Interns are eligible to participate in Company sponsored employee medical benefits in accordance with the terms of the plan.

Co‑Ops and Interns are eligible to participate in the following sick time benefits: up to 40 hours per calendar year; for employees who reside in the State of Washington, up to 56 hours per calendar year.

Co‑Ops and Interns are eligible to participate in Company’s consolidated retirement plan (pension).

For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits

This job posting is anticipated to close on 09/24/2026. The Company may however extend this time‑period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.

Ineligible for severance.

If you are under 18 years of age, you (the candidate) may need to obtain the necessary working papers or other documentation required by state law to start the assignment, as well as get a parent’s consent for the background check.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law.

We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers . Internal employees contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:

The anticipated base pay range for this position is : $27.00 per hour - $61.00 per hour Additional Description for Pay Transparency: The expected pay range for this position is between $27.00 per hour and $61.0 per hour but will be based on candidate's program year, discipline, degree and/or experience. Co‑Ops/Interns are eligible to participate in Company sponsored employee medical benefits in accordance with the terms of the plan. Co‑Ops and Interns are eligible for the following sick time benefits: up to 40 hours per calendar year; for employees who reside in the State of Washington, up to 56 hours per calendar year. Co‑Ops and Interns are eligible to participate in Company’s consolidated retirement plan (pension). For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits This job posting is anticipated to close on [08/27/2027]. The Company may however extend this time‑period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.

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 https://www.jnj.com/. Do Not Sell or Share My Personal Information Limit the Use of My Personal Information