Product Design Quality Engineer

Summary : This•Bothell, WA

About The Position

This is a Product Design Quality / Design Quality Engineering role in the medical device / regulated product domain. The engineer will support the complete product lifecycle, especially Design Control, Design Verification & Validation (V&V), Risk Management, CAPA, RCA, Process Validation, PMS, and regulatory compliance.

Requirements

  • Bachelor's or Master's degree in Mechanical Engineering, Electronics Engineering, Science, or equivalent.

Nice To Haves

  • Six Sigma Green Belt certification is preferred.
  • Master's degree: No prior experience is specified as mandatory.
  • Preferred experience includes Design Control, Design Verification & Validation (DV/V), Process Validation, Risk Management, CAPA, RCA, PMS, and medical-device/regulatory quality.

Responsibilities

  • Manage the Design Control process from design inputs through verification, validation, and design transfer.
  • Develop and execute process validation strategies using statistical/data-analysis methods.
  • Prepare and maintain Quality Plans and other quality engineering documentation.
  • Perform Design Verification (DV) and Design Validation (PV) planning and support execution.
  • Review product/system designs for quality, reliability, safety, performance, and manufacturability.
  • Perform Root Cause Analysis (RCA) for product and quality issues.
  • Manage CAPA activities, including investigation, corrective action, and effectiveness checks.
  • Support Risk Management/Risk Assessment throughout the product lifecycle.
  • Use Post-Market Surveillance (PMS) data to identify product quality issues and improvement opportunities.
  • Work with R&D, Manufacturing, Regulatory, Quality, and external stakeholders.
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