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.
We are seeking a skilled Quality Inspector to join our Quality Control team. In this role, you will ensure that our products comply with both internal and external standards through a variety of routine and non-routine inspections and evaluations. Your responsibilities will span across batch release, records management, and first article inspection activities, contributing directly to the safety and reliability of our medical device products.
Responsibilities
Responsibilities
Batch Release and Records Management
Audit batch records to ensure compliance with internal procedures, regulatory requirements, and industry standards.
Identify, document, and report batch nonconformances.
Organize and maintain batch records both physically and electronically according to company guidelines.
First Article Inspection
Perform moderately complex inspections and analyses to ensure products meet established specifications.
Conduct precise calculations and prepare detailed documentation of test results.
Compile data and prepare First Article Inspection (FAI) and First Inspection Report (FIR) reports.
General Quality Assurance
Apply Good Documentation Practices in all quality-related activities.
Provide training on test equipment and specialized GMP documentation requirements.
Support validation efforts, including the use of statistical software tools.
Implement updates and corrections to testing methods, equipment, and procedures.
Create and process Non-Conformance Reports (NCRs) using the company's quality systems.
