Precision QC Inspector – Medical Devices (Onsite)

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

Job summary

Experis Technology Group is seeking a Quality Control Inspector for a 12-month, onsite assignment in Portland. The role focuses on visual and physical inspections of raw materials, in-process components, and finished products to ensure quality specifications.

You will use precision measuring tools and lab equipment, maintain Lot History Records and batch records per GDP and FDA regulations, and report defects via NCRs.

Qualifications

• High school diploma or equivalent is 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 is desired.
• Familiarity with GDP and GMP and FDA regulations is beneficial.
• Eligible to work without sponsorship.

Responsibilities

• Inspect materials and finished products to ensure adherence to quality specifications.
• Utilize precision measuring tools and lab equipment to verify dimensions and performance.
• Maintain Lot History Records (LHR), batch records, and inspection logs per GDP and FDA regulations.
• Identify, classify, and report defects; initiate NCRs and assist with investigations.
• Monitor production processes for SOP and GMP compliance.
• Calibrate, clean, and maintain inspection equipment for accuracy.
• Collaborate with production and engineering teams to drive quality improvements.

Skills

Attention to Detail

Computer literacy (SAP / POMS / LIMS)

Regulatory knowledge (ISO 13485 & FDA

Communication skills

Education

High school diploma or equivalent

Associate or Bachelor’s degree in technical field

Tools

SAP

POMS

LIMS

Job description

Experis Technology Group is seeking a Quality Control Inspector for a 12-month, onsite assignment in Portland. The role focuses on visual and physical inspections of raw materials, in-process components, and finished products to ensure quality specifications.

You will use precision measuring tools and lab equipment, maintain Lot History Records and batch records per GDP and FDA regulations, and report defects via NCRs.