Quality Control Inspector

ABOUT ENOVIS

Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent and innovation, the Company's extensive range of products, services and integrated technologies fuels active lifestyles in orthopedics and beyond. For more information about Enovis, please visit What You’ll Do At Enovis we pay attention to the details. We embrace collaboration with our partners and patients, and take pride in the pursuit of scientific excellence - with the goal of transforming medical technology as we know it. Because that’s how we change the lives of patients for the better. And that’s how we create better together. Job Title Quality Control Inspector Reports To Sr Manager, Quality Assurance Location Vista, CA Business Unit Description Bracing and Supports Role Summary The Quality Control Inspector is responsible for performing quality inspections across incoming, in-process, and final inspection operations to ensure products meet established quality requirements and specifications. This role works closely with Quality, Manufacturing, Operations, and Supply Chain teams to identify and document quality issues, support production requirements, and ensure compliance with applicable procedures and standards. Key Responsibilities Perform and support incoming, in-process, final, and stock verification inspections in accordance with approved procedures, specifications, and sampling plans. Support in-process inspections and manufacturing quality activities to ensure product conformity throughout the production process. Execute and document First Article Inspections (FAI) and support qualification activities for new and changed products. Assist with validation and verification activities, including protocol execution, inspection support, data collection, and documentation review. Collaborate with Quality Engineers and cross-functional teams to support New Product Introduction (NPI) projects and successful product transfers into production. Coordinate Nonconforming Material Report (NCMR) activities, including identification, segregation, documentation, and disposition routing. Maintain accurate and compliant quality records, inspection reports, and support documentation in accordance with Quality Management System requirements. Work environment | Physical demands Ability to sit and stand for long periods of time. Ability to lift and carry 25 pounds. “Creating better together”. It’s the Enovis purpose, and it’s what drives us and empowers us every day on a global scale. We know that the power to create better - for our customers, our team members, and our shareholders - begins with having the best team, pursuing common goals, operating at the highest levels, and delivering extraordinary outcomes. Watch this short on creating the next generation of better together at Enovis: Better is... | Enovis We Offer a Comprehensive Benefits Package Which Includes Medical Insurance Dental Insurance Vision Insurance Spending and Savings Accounts 401(k) Plan Vacation, Sick Leave, and Holidays Income Protection Plans Discounted Insurance Rates Legal Services

EQUAL EMPLOYMENT OPPORTUNITY

Enovis provides equal employment opportunities based on merit, experience, and other work-related criteria without regard to race, color, ethnicity, religion, national origin, sex, age, pregnancy, disability, veteran status, or any other status protected by applicable law. We also strive to provide reasonable accommodation to employees’ beliefs and practices that do not conflict with Enovis policies and applicable law. We value the unique contributions that every employee brings to their role with Enovis. Important Visa & Sponsorship Information Currently, Enovis does not provide sponsorship for employment visas (e.g., H-1B) and will not offer such sponsorship in the future. Applicants must already have full-time work authorization in the United States, both now and in the future, without requiring sponsorship. Minimum Basic Qualifications High school diploma or equivalent required or a related technical discipline preferred. Minimum of 2-4 years of Quality Control, Inspection, Quality Assurance, or Manufacturing Quality experience in a regulated manufacturing environment (medical device preferred). Working knowledge of Quality Management System requirements, including ISO 13485, FDA 21 CFR Part 820/QMSR, and applicable quality system regulations. Demonstrated experience performing incoming, in-process, final, and first article inspections. Ability to read, interpret, and apply engineering drawings, specifications, bills of materials, and inspection criteria, including geometric dimensioning and tolerancing (GD&T). Proficiency with common inspection and test equipment, including calipers, micrometers, height gauges, comparators, pin gauges, and other precision measurement tools. Working knowledge of nonconformance management, root cause investigation techniques, corrective actions, and supplier quality processes. Experience utilizing ERP and electronic quality management systems (e.g., Oracle, SAP, Agile, NetSuite, ETQ, MasterControl, or equivalent). Proficient with computers and Microsoft Office applications, including Excel, Word, Outlook, and PowerPoint. Strong written and verbal communication skills with the ability to clearly document inspection results, nonconformances, and investigation findings. Demonstrated ability to work independently, prioritize multiple assignments, and make sound quality-related decisions within established procedures. #J-18808-Ljbffr Enovis