Quality Control Inspector - Medical Devices (Onsite)

Experis (Austria); Tigard (OR); On-site; USD 34,000 - 39,000; Full time

Job summary

Experis is seeking a Quality Control Inspector for an onsite 12-month assignment in Portland, OR. The role involves visual and physical inspections of materials and products, maintaining detailed records, and ensuring compliance with GDP and FDA standards.

The candidate will document deviations, manage NCRs, and support process control with collaboration across production and engineering teams to maintain high quality and regulatory adherence.

Qualifications

• High school diploma or equivalent required.
• Associate’s or Bachelor’s degree in a technical field preferred.
• 1+ years of experience in manufacturing, medical device, pharmaceutical, or similar regulated industries preferred.

Responsibilities

• Performs visual and physical inspections of raw materials, in-process components, and finished products to ensure quality specifications.
• Maintains Lot History Records (LHR), batch records, and inspection logs per GDP and FDA regulations.
• Identifies, classifies, and reports defects; initiates Non-Conformance Reports (NCR) and assists investigations.
• Monitors production processes to ensure adherence to SOPs and GMPs.
• Calibrates, cleans, and maintains inspection and testing equipment for accuracy.
• Collaborates with production and engineering teams to support quality improvements and regulatory compliance.

Skills

Attention To Detail

Computer Literacy

Technical Knowledge

Communication

Education

High school diploma or equivalent

Associate/Bachelor in technical field

Tools

SAP

POMS

LIMS

Job description

Experis is seeking a Quality Control Inspector for an onsite 12-month assignment in Portland, OR. The role involves visual and physical inspections of materials and products, maintaining detailed records, and ensuring compliance with GDP and FDA standards.

The candidate will document deviations, manage NCRs, and support process control with collaboration across production and engineering teams to maintain high quality and regulatory adherence.