QC Inspector II

Johnson & Johnson Innovative Medicine•Warsaw, IN

1d•Onsite

About The Position

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. 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 QC Inspector II. The QC Inspector II performs inspections on incoming products and materials.

Requirements

High School Diploma or equivalent is required.
Minimum of 2 years of related work experience is required.
Experience in inspection, manufacturing, or operations is preferred.
Knowledge of standard inspection techniques and tools (e.g., calipers, micrometers) is required.
Working knowledge of GD&T and blueprint interpretation and application.
Ability to perform hands‑on troubleshooting and problem solving.
Strong analytical, communication, and negotiation skills.
Ability to interact with, influence, and lead cross‑functional and cross‑business unit teams.
Strong tactical planning, execution, and organizational skills.
Demonstrated initiative and innovative problem‑solving in a fast‑paced, changing business environment.
Results‑driven, decisive, proactive, and responsive.

Responsibilities

Perform all job duties in full accordance with Worldwide Policies on Information Asset Protection.
Maintain passwords as confidential and protect Critical Business Information.
Understand, incorporate, and comply with all applicable laws, regulations, and internal policies related to DePuy’s business activities.
Adhere to the Health Care Compliance Program policies and Code of Conduct.
Complete routine inspections using applicable sampling plans and control plans to verify that products and services conform to quality, engineering, and Quality Assurance requirements.
Maintain accurate inspection records, filing systems, and documentation in compliance with quality standards and GMP regulations.
Perform sterile release activities, including review of documentation and products, as assigned.
Initiate nonconformance records for products that do not meet specifications.
Communicate business‑related issues and improvement opportunities to the next level of management.
Take initiative to address problems and contribute to quality and operational improvements.
Follow all Company guidelines related to Health, Safety, and Environmental (HSE) practices.
Ensure personal and Company compliance with all Federal, State, local, and Company regulations, policies, and procedures.
Perform other duties as assigned.