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Quality Engineer

  • Quality Engineer job type Posted on: Oct 28, 2026
  • Quality Engineer experience level Katalyst Healthcares & Life Sciences
  • Quality Engineer employment type Magna, Utah
  • Quality Engineer employment type Onsite
  • Quality Engineer salary Full-time

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Job Title :

Quality Engineer

Job Type :

Full-Time

Job Location :

Magna Utah United States

Remote :

No

Jobcon Logo Job Description :

Job Description

Job Description
Summary:
An opportunity is available for an experienced Quality Engineer to support quality systems, investigations, compliance, and continuous improvement within a regulated medical-device manufacturing environment.

Roles & Responsibilities:
  • Manage and investigate nonconforming materials, products and processes
  • Support the complete CAPA lifecycle, including investigation, documentation and effectiveness activities
  • Conduct structured Root Cause Analysis (RCA) and problem-solving
  • Maintain compliance with established Quality Management System requirements
  • Support compliance with ISO 13485 and FDA 21 CFR Part 820 / QMSR requirements
  • Identify and implement quality and manufacturing process improvements
  • Apply Lean Manufacturing and Six Sigma methodologies to reduce defects and improve operational performance
  • Support inspection-ready documentation and quality records
  • Collaborate with manufacturing, engineering and other cross-functional teams to resolve quality issues
Qualification:
  • Medical-device industry experience is mandatory
  • CAPA and Nonconformance Management experience
  • Quality investigations and Root Cause Analysis
  • Strong Quality Management Systems knowledge
  • ISO 13485 experience
  • FDA QMSR / 21 CFR Part 820 knowledge
  • Continuous improvement and process-improvement experience
  • Lean Manufacturing / Six Sigma knowledge
  • Experience working within highly regulated manufacturing environments

Jobcon Logo Position Details

Posted:

Oct 28, 2026

Reference Number:

e534e2e4

Employment:

Full-time

City:

Magna

Job Origin:

ziprecruiter

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Job Description

Job Description
Summary:
An opportunity is available for an experienced Quality Engineer to support quality systems, investigations, compliance, and continuous improvement within a regulated medical-device manufacturing environment.

Roles & Responsibilities:
  • Manage and investigate nonconforming materials, products and processes
  • Support the complete CAPA lifecycle, including investigation, documentation and effectiveness activities
  • Conduct structured Root Cause Analysis (RCA) and problem-solving
  • Maintain compliance with established Quality Management System requirements
  • Support compliance with ISO 13485 and FDA 21 CFR Part 820 / QMSR requirements
  • Identify and implement quality and manufacturing process improvements
  • Apply Lean Manufacturing and Six Sigma methodologies to reduce defects and improve operational performance
  • Support inspection-ready documentation and quality records
  • Collaborate with manufacturing, engineering and other cross-functional teams to resolve quality issues
Qualification:
  • Medical-device industry experience is mandatory
  • CAPA and Nonconformance Management experience
  • Quality investigations and Root Cause Analysis
  • Strong Quality Management Systems knowledge
  • ISO 13485 experience
  • FDA QMSR / 21 CFR Part 820 knowledge
  • Continuous improvement and process-improvement experience
  • Lean Manufacturing / Six Sigma knowledge
  • Experience working within highly regulated manufacturing environments

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