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Quality Engineering Technician

SMC Ltd. · Posted Nov 5, 2026

Santa Rosa, California, United States
2–3 years

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Provides focused quality-system and documentation support for validation-cage materials, retain-sample controls, data-package and template review, CAR/CAPA product containment and related containment actions, inspection-instruction updates, and DHR reviews to support complaint investigations or shipment release.

Responsibilities

Manage the validation cage by maintaining accurate material status and traceability
Release or move material only with documented authorization from Quality Engineers
Maintain retain-sample controls by accurately logging, organizing, retrieving, and disposing of retained product
Review quality data packages for completeness, accuracy, traceability, required records, and approvals
Prepare data-package documentation and update templates

Requirements

Associate or bachelor’s degree in quality, engineering, life sciences, manufacturing, or a related field
High school diploma or equivalent with at least 2–3 years of Quality Assurance experience
Nice to have: medical-device manufacturing experience
Nice to have: ISO 13485 familiarity
Nice to have: FDA quality-system requirements

Skills

good documentation practices review quality records data packages

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