Manufacturing Engineering Technician

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:
Quality

Job Sub Function:
Quality Control

Job Category:
Business Enablement/Support

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 Manufacturing Engineering Technician .

You will be responsible for:


* Conduct comprehensive non‑conformance investigations within the non‑conformance system, including NCR initiation, containment/bounding, product control and disposition, root‑cause analysis, corrective action, and full documentation.


* Lead cross‑functional kaizen events to identify root causes of nonconformance and ensure implementation of effective corrective and preventive actions.


* Apply failure‑analysis tools (for example, 5M) to perform robust investigations, analyze trends and data, and recommend improvements to processes, equipment, and systems.


* Propose and drive process and system enhancements; prepare and revise procedures and protocols using the document change control system.


* Implement corrective actions and continuous process improvements to reduce defects and improve product quality and reliability.


* Develop and deliver training and education to manufacturing teams on corrective actions, process changes, and quality best practices.


* Support internal and external audits and inspections by preparing required documentation, responding to observations, and executing corrective actions.

Qualifications / Requirements:

Required:


* Associate's or Bachelor's Degree in technical field (engineering, manufacturing, or related)


* 1 to 5 years of experience in regulated industry (medical, pharmaceutical, aerospace, etc.)

Preferred:


* Experience working in quality management system such as EtQ Reliance.


* Experience working in document management system such as PTC Windchill.
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