Quality Engineer - Medical Device Manufacturer

Job Title

Medical Device Quality Engineer

About Our Client

Our client is a medical device manufacturer specializing in electro-mechanical manufacturing processes. They are a growing organization as they are launching a brand new product line in which you will heavily support in your day-to-day responsibilities. They are ISO 13485 certified and their products and services are found in almost 50 countries. They offer an opportunity to make a meaningful impact on people's lives.

Job Description

Investigate and manage product complaints involving capital equipment, disposable products, serviced devices, field reports, and customer-reported issues while ensuring compliance with quality and regulatory requirements. Partner with Customer Support, Engineering, Manufacturing, Quality, and other cross-functional teams to assess complaints, determine investigation scope, prioritize risk, and involve suppliers when necessary. Escalate critical safety concerns, major quality issues, and investigation roadblocks to appropriate stakeholders in accordance with established procedures. Support regulatory reporting evaluations by maintaining thorough documentation and providing technical data needed for Quality and Regulatory decision-making. Maintain accurate, complete, and audit-ready complaint records, including investigation findings, root cause analysis, classifications, corrective actions, and customer communications. Ensure complaint investigations are closed in a timely manner and linked to risk management, CAPA, trend analysis, and continuous improvement initiatives.

CAPA & Continuous Improvement

Lead or support Corrective and Preventive Action (CAPA) activities resulting from complaint investigations and identified quality trends. Drive escalations for issues requiring improvements to products, processes, suppliers, servicing, labeling, design, or quality systems. Analyze complaint, CAPA, nonconformance, supplier, and post-market data to identify opportunities for quality and operational improvements.

Review Boards & Performance Metrics

Evaluate complaint, service, repair, and failure data to identify recurring issues, emerging risks, and adverse quality trends. Develop and report KPI metrics for Complaint Review Boards, CAPA Reviews, Management Reviews, Quality System Reviews, and audit support activities. Coordinate and lead Complaint Review Board meetings, including preparation of presentations, trend analyses, action items, and escalation summaries. Support CAPA Review Board activities by tracking progress, effectiveness, priorities, aging actions, and cross-functional follow-up requirements.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

The Successful Applicant

Bachelor's Degree (Engineering-related preferred) 4+ years of manufacturing experience within quality Understanding of ISO 9001 Experience with electro-mechanical processes Medical device experience is preferred Combination device experience is preferred Experience working with capital equipment Experience working with sterile products is preferred Understanding of ISO 14971 and UL 60601 is preferred CQE certification is preferred Six Sigma belt is preferred Sponsorship is not provided

What's on Offer

Base salary between $100k-$115k Health, dental, vision 401(k) matching 3 weeks PTO 4% annual bonus incentive

Job Summary

Sector: Engineering & Manufacturing Sub Sector: Production, Manufacturing Industry: Industrial / Manufacturing Where: Elk Grove Village Contract Type: Permanent Consultant name: Trevor Wojcik Job Reference: JN-092026-7100574