Biosurgery R&D Lifecycle Management Intern

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld 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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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.

Career Programs

Non-LDP Intern/Co-Op

Career Program

Raritan, New Jersey, United States of America

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

We are searching for the best talent for Biosurgery R&D Lifecycle Management Intern to be in Raritan, NJ.

• The Intern term is from May to August, 2027.
• Full time requirement (40 hours per week).

The Biosurgery Product Lifecycle Management (LCM) team supports a portfolio of medical devices used in surgical procedures. As products evolve over time, maintaining an understanding of their design history, performance requirements, and documentation is essential to supporting innovation, regulatory compliance, and continuous improvement initiatives.

This internship provides an opportunity to work in a cross-functional medical device development environment while gaining experience in laboratory testing, technical documentation, and product lifecycle management.

• Support the implementation and evaluation of laboratory test methods used to characterize medical device performance.
• Conduct experimental studies and analyze data to assess testing approaches and product attributes.
• Develop and document laboratory procedures, test methods, and study results in accordance with quality system requirements.
• Review and organize historical product and technical documentation to support lifecycle management activities.
• Collaborate with engineers and cross-functional partners to identify opportunities for process and documentation improvements.
• Present project findings and recommendations to technical stakeholders.

• Completion of Undergraduate Freshman year at an accredited University is required.
• Currently pursuing a Bachelor’s or Master's degree in Biomedical, Chemical, Materials Science, Mechanical Engineering, Chemistry, or related fields.
• Have a cumulative GPA of 2.8 or higher, which is reflective of all college coursework.
• Strong analytical and problem-solving skills.
• Interest in medical device development, product lifecycle management, or laboratory research.
• Excellent written and verbal communication skills.
• Experience with data analysis and laboratory environments is preferred.
• Familiar with Statistical tools, Minitab, Excel is plus.
• Lab experience is a plus.
• R&D experience in school or internship/co-op roles is a plus.
• Strong communication skills.

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…