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ENOVIS

Global medical technology company; orthopedic solutions

Quality Control Inspector

Inspection & TestConfirmed live in the last 24 hours
Full-timeVista, CA, USA$56.2k - $70.7kIn-person

About the Job

Requirements

  • A high school diploma or equivalent is required.
  • At least 2–4 years of Quality Control, Inspection, Quality Assurance, or Manufacturing Quality experience in a regulated manufacturing environment; medical device experience is preferred.
  • Working knowledge of Quality Management System requirements, including ISO 13485, FDA 21 CFR Part 820/QMSR, and applicable quality system regulations.
  • 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.
  • Proficiency with 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 using ERP and electronic quality management systems such as Oracle, SAP, Agile, NetSuite, ETQ, MasterControl, or equivalent.
  • Proficiency with computers and Microsoft Office applications, including Excel, Word, Outlook, and PowerPoint.
  • Ability to clearly document inspection results, nonconformances, and investigation findings.
  • Ability to work independently, prioritize multiple assignments, and make quality-related decisions within established procedures.
  • Ability to sit and stand for long periods and lift and carry 25 pounds.

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 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 projects and product transfers into production.
  • Coordinate Nonconforming Material Report activities, including identification, segregation, documentation, and disposition routing.
  • Maintain accurate and compliant quality records, inspection reports, and supporting documentation in accordance with Quality Management System requirements.

Desired Qualifications

  • Experience in a regulated manufacturing environment involving medical devices.
  • A related technical discipline.

About the Company

ENOVIS

Global medical technology company; orthopedic solutions

Enovis develops and sells medical devices and services to improve patient outcomes and restore mobility. Its business has two segments: Prevention & Recovery, which covers orthopedic braces, soft goods, vascular therapy, compression garments, and hot/cold therapy, and Reconstructive, which offers joint implants and minimally invasive surgical tools. The company differentiates itself with a broad, clinically focused portfolio, a global manufacturing and service network, and the Enovis Growth Excellence program to drive continuous improvement. Its goal is to deliver better patient outcomes and sustained growth by expanding its footprint and strengthening operations, including recent acquisition of LimaCorporate.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Wilmington, DE
Founded
2022

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