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Supplier Quality Engineer

Job in St George, Saint George, Washington County, Utah, 84770, USA
Listing for: Intellectt Inc
Full Time position
Listed on 2026-02-28
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
  • Engineering
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Location: St George

Location: Draper, UT (Greater Salt Lake City Area)

Duration: 9-Month Contract

Position Overview

We are seeking an experienced Supplier Quality Engineer to support a medical device client in Draper, Utah. This role is focused on addressing a backlog of aging supplier quality records and driving timely closure of open quality activities.

The ideal candidate will bring strong, hands-on experience in supplier-facing investigations, root cause analysis, and CAPA execution within a regulated medical device environment. This is a highly independent, execution-driven role requiring close collaboration with suppliers to resolve quality issues efficiently and compliantly.

Key Responsibilities
  • Perform triage and prioritization of aging supplier quality records; develop and execute structured action plans for closure
  • Lead supplier investigations, including root cause analysis and implementation of corrective and preventive actions
  • Manage, track, and close Supplier CAPAs, SCARs, NCRs, and NOCs
  • Work directly with suppliers to drive timely and effective resolution of quality issues
  • Support supplier risk assessments and updates to quality documentation
  • Ensure ongoing compliance with medical device Quality System requirements (FDA QSR and ISO 13485)
  • Identify and drive continuous improvement opportunities within supplier quality processes
Required Qualifications
  • 5–10 years of Supplier Quality experience within the medical device industry
  • Proven experience managing Supplier CAPAs, SCARs, NCRs, and supplier investigations
  • Strong ability to engage suppliers and independently drive root cause and corrective action activities
  • Solid working knowledge of FDA QSR and ISO 13485
  • Excellent analytical, documentation, and problem-solving skills
  • Strong communication and stakeholder-management capabilities
Preferred Qualifications
  • Experience in a high-volume manufacturing environment
  • Demonstrated success reducing quality backlogs and closing aged quality records
  • Experience supporting supplier audits and remediation activities
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