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Quality Control Inspector

Job in Tigard, Washington County, Oregon, USA
Listing for: Experis Technology Group
Full Time position
Listed on 2026-10-24
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 25 - 28 USD Hourly USD 25.00 28.00 HOUR
Job Description & How to Apply Below
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)

Description

We are seeking a “Quality Control Inspector” to join one of our leading healthcare clients.

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 .

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