Quality Control Inspector — Medical Devices & NPI

DJO, LLC

United States

On-site

USD 60,000 - 80,000

Full time

14 days+

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Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401(k) Plan

Job summary

Enovis in Vista, CA is hiring a Quality Control Inspector to perform and document verification inspections at various production stages. You will support NPI projects, product transfers, and maintain compliant quality records.

Minimum 2–4 years in a regulated manufacturing setting, with GD&T and use of precision inspection tools. This role emphasizes collaboration with Quality Engineers and cross-functional teams to ensure product conformity and strong documentation practices.

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.

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.