Design Quality Engineering Co-Op - Fall

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 Med Tech, 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.

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Career Programs

Non-LDP Intern/Co-Op

Career Program

Danvers, Massachusetts, United States of America

Design Quality Engineering Co-Op

Design Quality

Danvers, MA

Abiomed, part of Johnson & Johnson Med Tech, is a leading provider of medical devices that provide circulatory and respiratory support, with a mission of recovering hearts & saving lives. Abiomed's "Patients First!" culture drives our skilled workforce and strong relationships with clinicians. Our innovative product portfolio and robust pipeline provide us the incredible opportunity to bring lifesaving technology to more patients around the world than ever before.

Founded in 1981, Abiomed has a proven track record for growth, integrity and innovation.

The Design Quality Engineering Co‑Op will partner with new product development teams on one of the most dynamic innovations in Abiomed’s pipeline. This role will intend to develop design characterization analyses, assist with review and execution of design verification and validation activities and establish risk‑based methods of critical to quality (CtQ) monitoring. This opportunity will allow the candidate to advance their technical knowledge in Med Tech quality and compliance, design characterization, new product development and industry standards while also gaining experience with working with multidisciplinary teams to achieve impactful business results while advancing the future of innovation in Johnson & Johnson Med Tech at Abiomed.

• Analyze and review design documentation for characterization of critical to quality features (CtQs)
• Partner with new product development teams to address design tolerance analyses and apply risk management methodology based on associated outcomes
• Review and provide critical feedback to stakeholders on product design verification and validation activities, and test method validation strategies (as applicable)

• Enrolled in an accredited College/University pursuing a Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, Electrical Engineering, Computer/Software Engineering or a related field
• Completion of sophomore year by spring 2026
• Availability to work full‑time from July – December 2026
• Permanently authorized to work in the United States and not require sponsorship for employment visa status (e.g. H1‑B status) now or in the future
• Demonstrated ability to work independently as well as on a team
• Proficiency with Microsoft Office (Word, Excel, Power Point) and strong oral and written communication skills
• Minimum GPA of 3.0

• Basic knowledge of GD&T
• Basic knowledge of statistical techniques

$23.00/hr to $51.50/hr

The expected pay range for this position is between $23.00 per hour and $51.50 per hour but will be based on candidate's program year, discipline, degree and/or experience. Co‑Os/Interns are eligible to participate in Company sponsored employee medical benefits in accordance with the terms of the plan. Co‑Os 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‑Os and Interns are eligible to participate in the Company’s consolidated retirement plan (pension). For additional general information on Company benefits, please go to:  This job posting is anticipated to close on 07/13/26. The Company may however extend this time‑period, in which case the posting will remain…