Quality Engineer Intern

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

Job Function:
Career Programs

Job Sub Function:
Non-LDP Intern/Co-Op

Job Category:
Career Program

All Job Posting Locations:
Palm Beach Gardens, Florida, 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 Quality Engineering Intern to be in Palm Beach Gardens, FL.


* Internship typical term is 10-12 weeks May to August, 2026


* Full time requirement (40 hours per week)

Purpose:

Our rapidly growing Velys Robotics and Power Tools Operation is in need of a Quality Engineering Intern who provides overall quality assurance support of on-site manufacturing areas.

Ensures manufacturing areas are meeting good manufacturing practices, international organization for standardization and any other applicable standards.

 

You will be responsible for:



* Support measurement systems to monitor effectiveness of quality and reliability systems to identify, bracket, correct and prevent defects, communicating reports to management.


* Support multi-functional teams to handle sophisticated technical issues for manufacturing processes involved during Sustaining, New Product Introduction and/or Value Improvement Projects.


* Support Design Transfer Activities, including test method validation, process validation, creation of Inspection Plans, measurement system analysis and related protocols and reports.


* Provide Quality Engineering support to manufacturing including audits/assessments, verification/validation activities, CAPA and nonconformance investigation support,  and organizational change.

FDA CFR Part 820 and ISO 13485 regulations/standards focus.


* Be familiar and adhere to J&J environmental and safety policies and guidelines.

Immediately inform supervisors If there are any violations, deviations or hazards present related to health, safety or environment.

Qualifications / Requirements:

Education:

Must be enrolled in an accredited College/University pursuing a Bachelor’s or Master’s degree in the below or a related field:


* Mechanical Engineering


* Biomedical Engineering


* Electrical Engineering


* Computer / Software Engineering


* Indust...