Inspector II

We anticipate the application window for this opening will close on - 6 Nov 2026   Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life At Medtronic, you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. This role supports Quality Inspection activities within a manufacturing environment, ensuring raw materials, in-process products, and finished products meet established quality standards and regulatory requirements. The position plays a key role in verifying product conformance through inspection, testing, documentation review, and nonconformance management to support safe and effective product manufacturing. This position is based onsite in Eatontown, New Jersey. Minimal travel is expected. As an Inspector II, you will perform inspections and testing activities throughout the manufacturing process to ensure materials, components, and finished products meet quality requirements. This role works closely with manufacturing and quality teams to identify nonconformances, verify product acceptance criteria, and maintain accurate quality records. This position will also entail initiating nonconformance reports, quarantining products, dispositioning product associated with nonconformances, and closing nonconformance reports.                     Responsibilities may include the following and other duties may be assigned: • Inspect incoming raw materials for compliance with established specifications and quality requirements. • Perform in-process and final inspections of products, assemblies, and associated documentation. • Conduct testing of in-process materials and manufacturing equipment, including sealing equipment. • Evaluate products using inspection instructions, drawings, blueprints, specifications, and checklists. • Utilize measuring devices, gauges, and testing equipment to verify product conformity. • Initiate, investigate, and close nonconformance records in accordance with quality procedures. • Identify, locate, and quarantine potentially nonconforming product • Accept, reject, or identify products requiring rework based on inspection and testing results. Must Have: Minimum Requirements To be considered for this role, please ensure the minimum requirements are evident in your applicant profile.  • High School Diploma or equivalent and 1+ year of experience in manufacturing, quality inspection, quality assurance, or a regulated production environment.   Nice to Have • Experience using inspection procedures, work instructions, drawings, or product specifications. • Experience utilizing measuring devices, testing equipment, or inspection tools. • Ability to document inspection results and maintain accurate quality records. • Basic knowledge of manufacturing or supply chain operational processes and quality procedures. • Experience in medical device, pharmaceutical, biotechnology, or other regulated manufacturing industries. • Experience reviewing Device History Records (DHRs), batch records, or production documentation. • Experience with nonconformance management and corrective action processes. • Knowledge of Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Good Tissue Practices (GTP), a