Quality Engineering Manager

Hobson Associates

  • Lincoln, NE
  • 6 days ago
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    Skills

    • Continuous Improvementunmatched
    • Corrective and Preventative Action (CAPA) Systemsunmatched
    • Engineering Managementunmatched
    • Environmental Complianceunmatched
    • Leadershipunmatched
    • Lean Six Sigmaunmatched
    • Manufacturingunmatched
    • Medical Equipmentunmatched
    • Molding Processesunmatched
    • Operational Improvementunmatched
    • Operationsunmatched
    • Performance Managementunmatched
    • Problem Solving Skillsunmatched
    • Production Volumeunmatched
    • Quality Engineeringunmatched
    • Quality Managementunmatched
    • Regulationsunmatched
    • Sterilizationunmatched

    Description

    If you've led quality in a high-volume manufacturing environment where compliance, production, and continuous improvement intersect, this is a role where your impact is immediately felt.We're partnered with a global medical technology manufacturer seeking a Quality Engineering leader to own site-level quality systems at a critical high-volume production facility in the Midwest.This is a hands‑on leadership role where quality directly drives production performance, product release, and customer confidence.Role Impact You'll own the quality engineering function for a key manufacturing site, shaping execution, compliance, and continuous improvement:Lead site quality systems and QE support across high-volume manufacturing (molding, assembly, packaging, sterilization, release)Own validation strategy across processes, equipment, materials, and product changesDrive reduction in defects, complaints, and waste through effective corrective actionsLead audit readiness and regulatory inspection supportPartner with Operations, Engineering, and Regulatory to improve performance and solve issues at the sourceBuild and develop a small quality teamEmbed Lean/Six Sigma into daily operations and improvement effortsSupport a 24/7 manufacturing environmentWhat You Bring Bachelor's in Engineering or related field required5+ years in quality, including 3+ in medical device or regulated manufacturingStrong validation, CAPA, and quality/statistical tools experienceHigh-volume manufacturing background strongly preferredProven leadership and cross‑functional influenceMust be a U.S. permanent resident or green card holder.Full benefits#J-18808-Ljbffr

    Numbers & Facts

    LocationLincoln, NE

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