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Manufacturing Quality Engineer

Job in Omaha, Douglas County, Nebraska, 68102, USA
Listing for: Katalyst Healthcares & Life Sciences
Full Time position
Listed on 2026-06-28
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Production QC/QA, Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers
  • Engineering
    Quality Engineering, Regulatory Compliance Specialist
Job Description & How to Apply Below

Manufacturing Quality Engineer

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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