Quality Engineer: Validation, CAPA & Continuous Improvement

MME group Inc.

Vadnais Heights (MN)

On-site

USD 65,000 - 95,000

Full time

14 days+

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Job summary

MME group Inc. in Minnesota seeks a qualified Quality Engineer to support development and sustaining quality activities across assigned programs, focusing on part validation, qualification, and ongoing regulatory compliance.

You will participate in Stage-Gate product realization, lead IQ/OQ/PQ validation efforts, drive root cause analysis, CAPA, and continuous improvement with Lean Six Sigma. Collaboration with Manufacturing, Engineering, and Supply Chain is essential.

Qualifications

  • BS degree in engineering or equivalent work experience.
  • 4+ years’ experience in a regulated manufacturing environment.
  • Experience executing IQ, OQ, and PQ validation activities.
  • Working knowledge of ISO 13485 and FDA quality system requirements.
  • Experience supporting customer audits and quality discussions.
  • Strong root cause analysis and corrective action experience.
  • Ability to manage multiple projects concurrently.
  • Knowledge of print reading, GD&T, and cosmetic specifications.
  • Experience with change control and documentation.

Responsibilities

  • Supports development and sustaining quality activities for assigned programs, including part validation, qualification, and ongoing compliance.
  • Participates in the organization’s Stage-Gate approach to product realization.
  • Supports and executes validation activities, including IQ, OQ, and PQ protocols and reports, as directed.
  • Carries out quality planning activities including Process FMEAs, and Control Plans. Prepares work instructions and inspection instructions.
  • Acts as the primary quality contact for assigned customers, supporting customer quality concerns, investigations, and corrective actions.
  • Participates in the creation and management of CAPAs, SCARs, RMAs, and sustaining programs.
  • Supports disposition of internally produced nonconforming material.
  • Works collaboratively with Manufacturing, Engineering, and Supply Chain to provide consultation and guidance on quality issues.
  • Serves on the internal audit team and leads customer audits for assigned programs and products, including audit preparation, participation, documentation, and coordination of responses and corrective actions, while supporting ISO 13485 and regulatory audits as assigned.
  • Drives continuous improvement by analyzing quality data, identifying trends, and partnering with cross-functional teams to improve product and process performance.
  • Drive continuous improvement in manufacturing by using Lean/Six Sigma tools and production data to reduce defects, scrap, rework, and customer complaints.
  • Lead cross‑functional problem‑solving events (8D, DMAIC, A3), perform root cause analysis, and implement effective, sustainable CAPA for chronic quality and production issues.
  • Partner with Production, Engineering, and Processing to standardize improved methods, update control plans and work instructions, and ensure process adherence on the shop floor.
  • Coach and train operators, technicians, and supervisors in basic quality tools, standard work, and problem‑solving methods to strengthen a culture of continuous improvement.
  • Serve as the primary owner of NCR and MRB processes, driving investigation, disposition, risk assessment, corrective actions, and closure of nonconforming material issues.

Skills

Root cause analysis
CAPA/SCAR/RMA processes
Lean Six Sigma
Cross-functional collaboration
Problem-solving (8D/DMAIC/A3)
Quality systems (ISO 13485, FDA QSR)
Print reading and GD&T
Project management
Documentation control

Education

B.S Degree in Engineering or equivalent work experience

Tools

Epicor ERP

Job description

MME group Inc. in Minnesota seeks a qualified Quality Engineer to support development and sustaining quality activities across assigned programs, focusing on part validation, qualification, and ongoing regulatory compliance.

You will participate in Stage-Gate product realization, lead IQ/OQ/PQ validation efforts, drive root cause analysis, CAPA, and continuous improvement with Lean Six Sigma. Collaboration with Manufacturing, Engineering, and Supply Chain is essential.

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