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Quality Control Inspector

Job in Portland, Multnomah County, Oregon, 97204, USA
Listing for: LanceSoft Inc
Full Time position
Listed on 2026-03-06
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector
  • Manufacturing / Production
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Title: Quality Control Inspector

Location: Portland, OR – 97224

Duration: 05/04/2026 to 11/04/2026 (6 Months)

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 (Client) 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.
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.
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