Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.
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DePuy Synthes Companies of Johnson & Johnson is the largest, most comprehensive orthopedic and neurological business in the world. DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Our broad array of inspired, innovative and high-quality offerings, help advance the health and wellbeing of people around the world.
As a Quality Inspector 3, you will play a key role in ensuring that our products meet both internal and external standards. You will perform a wide range of inspections and evaluations-both routine and complex-across inspection and testing, batch release, records management, first article inspections, and 3D CMM. Your work will contribute directly to maintaining our high standards in the medical device industry.
Responsibilities
Inspection and Testing
- Conduct inspections on finished goods, components, incoming materials, and pre-service materials using measurement tools and observation.
- Document inspection results, compare with specifications, and input data into systems.
- Accept, reject, or reroute products based on inspection findings.
- Communicate quality concerns with other departments and recommend corrective actions.
- Act as Subject Matter Expert (SME) for specific measurement systems (e.g., SWR meter, CMM)
Batch Release and Records Management
- Audit batch records for regulatory and procedural compliance.
- Identify and report batch nonconformities.
- Manage physical and digital batch documentation.
First Article Inspection (FAI)
3D Coordinate Measuring Machines (CMM)
General Quality Assurance
Apply Good Documentation Practices consistently.
Train colleagues on testing equipment and quality standards.
Support validation activities with statistical tools.
Implement procedural changes and equipment updates.
Manage and execute NCRs and CAPA actions in quality systems.
