Quality Control Inspector — Regulated Manufacturing

ManpowerGroup; Tigard (OR); On-site; USD 41,000 - 45,000; Full time

Benefits offered by this job

Medical plan

Dental plan

Vision plan

401(k) with match

Weekly pay

Job summary

ManpowerGroup is seeking an Inspector, Quality Control for a manufacturing client in Tigard, OR. This role supports the Quality Assurance Department, performing visual and dimensional inspections to ensure product quality and regulatory compliance.

Ideal candidates have attention to detail, strong communication, and experience with GMPs and ISO 13485, FDA 21 CFR Part 820; familiarity with SAP, Excel, Outlook and Teams is a plus.

Qualifications

• High school diploma or equivalent; Associates or Bachelors degree in a technical field preferred.
• 1+ years of manufacturing experience, preferably in medical device/pharma or regulated industries.
• Understanding of ISO 13485 and FDA 21 CFR Part 820 regulations.
• Proficiency with SAP, MS Excel, Outlook, and Teams.

Responsibilities

• Perform visual and physical inspections of raw materials, in-process components, and finished products to ensure quality specifications.
• Use precision measuring tools and lab equipment to verify dimensions and performance (SmartScope Zone 3 and CMM highly preferred).
• Maintain Lot History Records, batch records, and inspection logs per GDP and FDA regulations.
• Identify, classify, and report defects; initiate NCRs and assist investigations.
• Monitor production processes for compliance with SOPs and GMPs.

Skills

Attention to detail

Communication skills

Proactive approach

Education

Associates or Bachelors degree in a technical field

Tools

SAP

MS Excel

Outlook

Teams

Job description

ManpowerGroup is seeking an Inspector, Quality Control for a manufacturing client in Tigard, OR. This role supports the Quality Assurance Department, performing visual and dimensional inspections to ensure product quality and regulatory compliance.

Ideal candidates have attention to detail, strong communication, and experience with GMPs and ISO 13485, FDA 21 CFR Part 820; familiarity with SAP, Excel, Outlook and Teams is a plus.