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Quality Engineering Technician (NPI & V&V)

Spherion - San Jose, CA

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$50-60 /h
PAY RATE
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Milpitas, CA
LOCATION

Job Description

As posted by the hiring company

Job Overview:

**Position Type: **6 Month Contract

**Pay Range: **$50 to $60/hour

**Schedule: **Monday through Friday, standard day shift. Candidates must be open to overtime as needed.

Position Overview

The Quality Technician supports Verification & Validation (V&V) testing and New Product Introduction (NPI) activities .This individual will work closely with R&D, Quality, and Manufacturing teams supporting surgical robotic systems and related mechanical/electronic components.

Key Responsibilities

Verification & Validation (V&V) Support

  • Execute V&V test protocols, including functional, reliability, and performance testing

  • Set up test fixtures, equipment, and test samples per approved procedures

  • Accurately record, analyze, and report test data in accordance with GDP (Good Documentation Practices)

  • Identify, document, and escalate nonconformances or unexpected results

  • Support investigation and root cause analysis of test failures

  • Partner with R&D during design and development phases to support product builds and testing. Assist in prototype builds, design iterations, and engineering studies

  • Provide feedback on testability, manufacturability, and quality risks

  • Ensure all activities comply with FDA, ISO 13485, and internal quality system requirements. Maintain accurate documentation, including test records, logs, and reports

  • Assist with document control, including reviewing and updating procedures and test methods

  • Ability to support projects as assigned.

Qualifications

Education & Experience

  • Associate’s degree in a technical field (e.g., Engineering Technology, Life Sciences) or equivalent experience

  • 2+ years of experience in a quality, manufacturing, or test role (medical device preferred)

  • Experience with test execution and data collection in a regulated environment

  • Familiarity with V&V processes and documentation. Working knowledge of FDA QSR (21 CFR Part 820) and/or ISO 13485

  • Strong attention to detail and documentation accuracy. Ability to read and interpret engineering drawings and specifications

  • Effective communication and teamwork skills

  • Hands-on experience with lab/test equipment and measurement tools. Basic data analysis skills (Excel or similar tools)

  • Experience with quality systems (eQMS) is a plus

Work Environment

  • Combination of laboratory, manufacturing floor, and office settings
  • May require lifting, standing for extended periods, and handling test equipment