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Quality Control Tech II

Johnson & Johnson
United Statesfull_timeVerifiedPosted 24 Mar 2026
💰 $73,370/yr($45,100/yr$73,370/yr)

About the role

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 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:

Raynham, Massachusetts, United States of America

Job Description:

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/.

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

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.

Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

We are searching for the best talent for a Quality Control Technician II.

The Quality System Technician II is responsible for ensuring orthopedic medical devices and components meet stringent quality, safety, and performance standards. This role performs detailed technical inspections, supports regulatory compliance, and works closely with engineering and manufacturing teams in a highly regulated environment.

Key Responsibilities:

Technical Inspection

  • Perform dimensional, visual, and functional inspections of incoming materials, in-process components, and finished medical devices.

Blueprint & Specification Review

  • Read, interpret, and apply complex engineering drawings and technical specifications, including Geometric Dimensioning and Tolerancing (GD&T).

Precision Measurement

  • Utilize high-precision inspection tools such as calipers, micrometers, height gauges, thread gauges, optical comparators, and related measurement software.

Advanced Inspection Equipment

  • Operate and support automated inspection systems including Coordinate Measuring Machines (CMMs), Sylvac Scan systems, and digital optical comparators. Troubleshooting experience is a plus.

Quality Documentation & Compliance

  • Maintain accurate inspection records, generate First Article Inspection (FAI) reports, and ensure compliance with FDA and other applicable medical device regulations.

ERP & Material Flow Management

  • Manage product movement and inspection status within ERP systems such as

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Company

Johnson & Johnson

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