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, andsolutions 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:
Raritan, New Jersey, 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

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).

Purpose:

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.

You will be responsible:


* 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.

Qualifications / Requirements:


* Completion of Undergraduate Freshman year at an accredited University is required.


* Currently pursuing a Bachelor's or Master's degree in Biome...