Quality Control Inspector
Job in
Portland, Multnomah County, Oregon, 97204, USA
Listed on 2026-03-06
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
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.
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.
- 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.
- 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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