Quality Control Inspector

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

Job Title: Quality Control Inspector

Location: 16125 SW 72nd Ave, Portland, OR 97224

Duration: 12 months

Work Arrangement: 100% Onsite

Shift: 7:00 AM – 3:30 PM

Pay Range: $25 - $28 per hour (W2)

We are seeking a “Quality Control Inspector” to join one of our leading healthcare clients.

Description

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 (NCR) 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.

Common 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.

We are looking for the candidate who are eligible to work with any employers without sponsorship