Quality Control Inspector
Reference Number: 415175
Posted: 10/21/2026
Job Type: Contract
- Industry: Science and Research
Job Title: Quality Control Inspector
Location: 16125 SW 72nd Ave, Portland, OR 97224
Duration: 12 months
Work Arrangement: 100% Onsite
Shift: 7:00 AM – 3:30 PM
Pay Range: $25 - $28 per hour (W2)
We are seeking a “Quality Control Inspector” to join one of our leading healthcare clients.
Description
The Inspector performs basic routine inspection of electronic, electro-mechanical and/or mechanical materials, components and sub-assemblies received, in process of manufacture, or manufactured, for conformance with quality assurance standards.
Key Job Duties and Responsibilities
Inspection & Testing:
Performs visual and physical inspections of raw materials, in-process components, and finished products to ensure they meet quality specifications. Uses precision measuring tools and lab equipment to verify product dimensions and performance.
Documentation & Compliance:
Accurately maintains Lot History Records (LHR), batch records, and inspection logs in compliance with Good Documentation Practices (GDP) and FDA regulations.
Defect Management:
Identifies, classifies, and reports defects. Manages non-conforming material by initiating Non-Conformance Reports (NCR) and assisting with investigations.
Process Control:
Monitors production processes to ensure adherence to standard operating procedures (SOPs) and Good Manufacturing Practices (GMPs).
Equipment Maintenance:
Calibrates, cleans, and performs routine maintenance on inspection and testing equipment to ensure accuracy.
Collaboration:
Works with production and engineering teams to support quality improvements, provide feedback on product quality, and ensure regulatory compliance.
Key Competencies
Attention to Detail:
High level of accuracy in documentation and inspection.
Computer Literacy:
Proficient in using software like SAP, POMS, or Laboratory Information Management Systems (LIMS).
Technical Knowledge:
Understanding of ISO 13485 and FDA 21 CFR Part 820 regulations.
Communication:
Ability to clearly report deviations and collaborate in a team environment.
Common Educational/Experience Requirements
- High school diploma or equivalent is required. Associate’s or Bachelor’s degree in a technical field preferred.
- Previous experience in manufacturing, particularly in medical device, pharmaceutical, or similar regulated industries is highly desired. 1+ years of experience desired.
We are looking for the candidate who are eligible to work with any employers without sponsorship.
If you’re interested, please click “Apply” button.
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