Production Associate II

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:
Supply Chain Manufacturing

Job Sub Function:
Manufacturing Assembly

Job Category:
Business Enablement/Support

All Job Posting Locations:
Danvers, Massachusetts, 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 Production Associate II to be in Danvers, MA.

Job Summary

The Cleanroom Production Associate II will be responsible for assembling, inspecting and testing high quality medical devices while working within a controlled manufacturing system.

Duties & Responsibilities


* Process polymer materials to compose, test, or apply on medical devices per approved manufacturing procedures


* Assemble plastic and metal components into medical devices in accordance with approved manufacturing procedures


* Perform in-process quality checks on subassemblies and finished product


* Utilize small hand tools, calibrated instruments, measurement equipment, microscopes, and test fixtures


* Participate in line meetings as needed


* Work with engineers and technicians to resolve line issues and suggest improvements


* Maintain clean room integrity by using proper attire and adherence to clean room environment practice and procedures


* Fully understand and maintains accurate records/documentation related to quality, work in progress, test results, labor (e.g., timecards), and special projects


* Apply workstation practices and line clearance in daily activities


* Adhere to general safety rules, manufacturing procedures, company policies and procedures, QSR, and FDA regulations

Qualifications - External


* High School Graduate or equivalent manufacturing experience


* 4 or more years of medical device manufacturing experience with relevant microscope experience or 2 or more years of intensive microscope job related experience in a Class III medical device company


* Must have good hand-eye coordination and manual dexterity to work with small plastic and metal components in a high volume manufacturing setting


* Knowledge of lean, six sigma, kaizen, and continuous improvement initiatives a plus.


* Ability to read, write, and spe...