Quality Control Inspector Experis

•3.3 Tigard, OR Job Details Contract $25

•$28 an hour 18 hours ago Qualifications High school diploma or

GED Full 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 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.

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 . If you're interested, please click "Apply" button.