Stand out for this role — generate a tailored resume and cover letter in about a minute.
Johnson & Johnson’s Biosurgery R&D Lifecycle Management Intern in Raritan, NJ, offers hands-on experience in medical device development within a cross-functional team. The internship runs May–August 2027 for 40 hours per week, focusing on lifecycle management, lab testing, and technical documentation.
You will support test methods, analyze data, document procedures, review history, and collaborate with engineers to drive process improvements and present findings to stakeholders.
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.
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 https://www.jnj.com/medtech
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.
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 the alternative long-term status that does not require company sponsorship.
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.