Manufacturing Quality Engineer

Karwell Technologies

  • Omaha, NE
  • 30+ days ago

    Highlights

    The ideal candidate will drive quality improvements, investigate non-conformances, lead root cause analysis activities, and collaborate with cross-functional teams to maintain a robust Quality Management System (QMS). Lead root cause investigations using methodologies such as 5 Whys, Fishbone, Pareto Analysis, and FMEA.

    Numbers & Facts

    LocationOmaha, NE

    Description

    Job Description:
    We are seeking a Manufacturing Quality Engineer to support manufacturing operations by ensuring products meet quality standards, regulatory requirements, and customer expectations. The ideal candidate will drive quality improvements, investigate non-conformances, lead root cause analysis activities, and collaborate with cross-functional teams to maintain a robust Quality Management System (QMS).
    Responsibilities:
    • Support daily manufacturing operations to ensure compliance with quality standards and procedures.
    • Investigate product defects, non-conformances, deviations, and customer complaints.
    • Lead root cause investigations using methodologies such as 5 Whys, Fishbone, Pareto Analysis, and FMEA.
    • Develop, implement, and monitor Corrective and Preventive Actions (CAPA).
    • Analyze quality metrics and identify opportunities for continuous improvement.
    • Review and approve manufacturing procedures, work instructions, SOPs, and quality documentation.
    • Support process validation, equipment qualification, and change control activities.
    • Conduct internal audits and participate in customer, regulatory, and certification audits.
    • Collaborate with Manufacturing, Engineering, Supply Chain, Operations, and Quality teams.
    • Monitor Statistical Process Control (SPC) data and implement process improvements.
    • Ensure compliance with applicable regulations and quality standards.
    • Support risk management and quality planning activities.

    Requirements:

    • Bachelor's degree in mechanical, Industrial, Manufacturing, Biomedical Engineering.
    • 3+ years of experience in Quality Engineering, Manufacturing Quality, or Quality Assurance.
    • Experience in a manufacturing environment.

    Required Skills:

    • Quality Management Systems (QMS).
    • CAPA Management.
    • Root Cause Analysis.
    • Non-Conformance Management.
    • Change Control.
    • Statistical Process Control (SPC).
    • FMEA (Failure Mode and Effects Analysis).
    • Risk Management.
    • Process Improvement.
    • Data Analysis and Reporting.
    • Technical Documentation.

    Preferred Qualifications:

    • Experience with:
      • ISO 9001
      • ISO 13485
      • AS9100
      • IATF 16949
      • GMP/GxP environments
    • Knowledge of Lean Manufacturing and Six Sigma methodologies.
    • Experience with validation and qualification activities.
    • ASQ certifications such as American Society for Quality CQE or CQA preferred.

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