Inspector, Quality Control

Experis Technology Group; Tigard (OR); On-site; USD 41,000 - 45,000; Full time

Job summary

ManpowerGroup Global, Inc. is helping a manufacturing leader hire an Inspector, Quality Control in Tigard, OR. You will join the Quality Assurance team to inspect raw materials, in-process parts, and finished goods to ensure they meet specifications.

The role requires keen attention to detail, solid communication, and reliability in a regulated environment. You will maintain records, report defects, and support GMP and GDP compliance through disciplined inspection routines.

Qualifications

• High school diploma or equivalent; technical degree preferred.
• 1+ years of manufacturing experience, preferably in regulated industries.
• Familiarity with ISO 13485 and FDA 21 CFR Part 820.
• Proficient with SAP, Excel, Outlook, and Teams.
• Strong attention to detail and clear communication.

Responsibilities

• Perform visual and physical inspections of materials to meet specs.
• Use precision tools and equipment to verify dimensions.
• Maintain Lot History Records and inspection logs per GDP/FDA guidelines.
• Identify and report defects; manage non-conforming material.
• Monitor SOPs and GMP adherence in production.

Skills

Attention to detail

Communication skills

Proactive approach

Education

High school diploma or equivalent

Associates or Bachelors degree in a technical field

Tools

SAP

MS Excel

Outlook

Teams

Job description

Our client, a leader in the manufacturing industry, is seeking an Inspector, Quality Control to join their team. As an Inspector, Quality Control, you will be part of the Quality Assurance Department supporting the production and inspection teams. The ideal candidate will have keen attention to detail, strong communication skills, and a proactive approach, which will align successfully in the organization.

Job Title

Inspector, Quality Control

Location

Tigard, OR

Pay Range

30/hr -33/hr on w2

What's the Job?

• Perform visual and physical inspections of raw materials, in-process components, and finished products to ensure they meet quality specifications.
• Use precision measuring tools and lab equipment to verify product dimensions and performance, including prior use of SmartScope Zone 3 and CMM highly preferred.
• Accurately maintain Lot History Records (LHR), batch records, and inspection logs in compliance with Good Documentation Practices (GDP) and FDA regulations.
• Identify, classify, and report defects, managing non-conforming material by initiating Non-Conformance Reports (NCR) and assisting with investigations.
• Monitor production processes to ensure adherence to standard operating procedures (SOPs) and Good Manufacturing Practices (GMPs).

What's Needed?

• High school diploma or equivalent; Associates or Bachelors degree in a technical field preferred.
• Previous experience in manufacturing, particularly in medical device, pharmaceutical, or similar regulated industries, with 1+ years of experience desired.
• Understanding of ISO 13485 and FDA 21 CFR Part 820 regulations.
• Proficiency in using software like SAP, MS Excel, Outlook, and Teams.
• Strong attention to detail and excellent communication skills to report deviations and collaborate effectively.

What's in it for me?

• Opportunity to work in a regulated industry with a focus on quality and compliance.
• Engage in meaningful work supporting product safety and excellence.
• Gain valuable experience with industry-standard inspection tools and procedures.
• Join a team committed to continuous improvement and professional growth.
• Work in a supportive environment that values diversity and inclusion.

Upon completion of waiting period, consultants are eligible for:

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account
• Health Flexible Spending Account
• Dependent Care Flexible Spending Account
• Supplemental Life Insurance
• Short Term and Long Term Disability Insurance
• Business Travel Insurance
• 401(k), Plus Match
• Weekly Pay