Inspector, Quality Control

GTT

Portland, OR

JOB DETAILS
SKILLS
Banking Services, Biology, Biotech and Pharmaceutical, Bug Tracking/Defect Management, Code of Federal Regulations, Debugging Skills, Dental Insurance, Detail Oriented, Documentation, Electromechanics, Equipment Maintenance/Repair, FDA (Food and Drug Administration), Financial Services, Fortune 500 Customers, GMP (Good Manufacturing Practices), Healthcare, ISO (International Organization for Standardization), Industry Standards, International Health, Investigative Reports, Laboratory Equipment, Laboratory Information Management System (LIMS), Maintain Compliance, Manufacturing, Manufacturing Operations, Manufacturing/Industrial Processes, Medical Diagnosis, Medical Equipment, Nutrition, Operational Support, Procedure Implementation, Process Control Engineering, Product Documentation, Production Control, Quality Assurance, Quality Assurance Methodology, Quality Control, Quality Metrics, Quality Monitoring, Regulatory Requirements, Retail, Retirement Funds, SAP, Standard Operating Procedures (SOP), Test Equipment, Testing, Theater Production, Vision Plan
LOCATION
Portland, OR
POSTED
30+ days ago
Primary Job Title:
Quality Control Inspector

Alternate/Related Job Titles:
Quality Assurance Inspector
Manufacturing Quality Inspector
Incoming Quality Inspector
QA/QC Inspector
Production Quality Inspector

Location:
Portland, OR

Onsite Flexibility:
Onsite

Contract Details (Contract roles only):
  • Position Type: Contract
  • Contract Duration: 6 Months
  • Start: As Soon As Possible
  • Shift: 8 AM – 4:30 PM
Job Summary:
The Quality Control Inspector performs routine inspections of electronic, electro-mechanical, and mechanical materials, components, and sub-assemblies during various stages of production. This role ensures that materials and finished products meet quality assurance standards and regulatory requirements. The inspector supports manufacturing operations by verifying product specifications, documenting results, and helping maintain compliance with industry standards.

Key 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.
Required Experience:
  • High school diploma or equivalent required.
  • 1+ years of experience in manufacturing or quality inspection environments.
  • Experience performing visual and physical inspections of manufactured components.
  • Familiarity with documentation practices in regulated manufacturing environments.
Nice-to-Have Experience:
  • Associate’s or Bachelor’s degree in a technical field.
  • Experience in medical device, pharmaceutical, or other regulated manufacturing industries.
Required Skills:
  • Quality inspection and testing techniques
  • Attention to detail in documentation and inspection
  • Understanding of manufacturing processes and quality standards
Preferred Skills:
  • SAP, POMS, or Laboratory Information Management Systems (LIMS)
  • Knowledge of ISO 13485 and FDA 21 CFR Part 820 regulations
  • Experience with precision measuring tools and lab equipment
  • Investigation and reporting of non-conforming materials
Additional Skills:
  • Lot History Record (LHR) documentation
  • Good Documentation Practices (GDP)
  • Good Manufacturing Practices (GMP) adherence
  • Non-Conformance Report (Client) initiation and investigation support
  • Production process monitoring and quality feedback
Benefits:
  • Medical, Vision, and Dental Insurance Plans
  • 401k Retirement Fund
About the Client:
Global Healthcare Innovator
We're a leading healthcare company dedicated to improving lives worldwide. Our diverse portfolio includes medical devices, diagnostics, nutrition products, and branded generics. We're committed to developing groundbreaking technologies that address critical healthcare challenges and empower people to live healthier lives.
Join our team and:
  • Work on cutting-edge projects
  • Contribute to global healthcare advancements
  • Experience diverse cultures and geographies
  • Discover a rewarding career with a company that cares.
About GTT:
GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking, financial services, technology, life sciences, biotech, utilities, and retail sectors throughout the U.S. and Canada.

Job Number:
26-02148
Hashtags:
#gttjobs  #LI-GTT  #LI-Onsite

About the Company

G

GTT