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

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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
• Industrial Engineering

Experience and Skills:

Required:

• Must have completed two semesters in school by the start of the co-op (rising Sophomore or above), SENIOR GRADE LEVEL
• Must be familiar with basic statistics concepts/terminology (If not in an engineering application- other roles are acceptable (i.e. budget management from a club, or any experience working with numbers)
• Detail-oriented, highly organized and able to manage multiple tasks.
• Ability to work independently as well as on a team.
• Proficient with Microsoft Office (Word, Excel, Power Point) and have strong oral and written communication skills.
• A minimum GPA of 3.0
• Availability to work Full-time., 40 hours per week on-site from August – December.
• 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 an alternative long-term status that does not require company sponsorship.

Preferred:

• Demonstrated leadership/participation in campus programs and/or community service activities.
• Advanced familiarity with statistics concepts/terminology (either from previous co-ops or classwork)
• Previous quality engineering related experiences.
• Knowledge of FDA or regulatory guidance.
• Medical related experience (previous co-op at medical device company, working volunteering at a hospital, etc.).
• Understanding of process validation, non-conformance material management, test method validation, measurement system analysis, design of experiments.
• Failure analysis/root cause understanding.
• Experience with statistics software (e.g. Minitab).

Other:

• This position will require less than 10% travel

Ineligibility for severance.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https: //www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.

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