Medical Device Quality Inspector - Onsite, 12-Month

Abbott

Portland (OR)

On-site

USD 55,000 - 75,000

Full time

14 days+
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Benefits offered by this job

Medical and Prescription Drug Plans
Dental Plan
Vision Plan
Health Savings Account
Flexible Spending Accounts
Supplemental Life Insurance
Short Term Disability
Long Term Disability
Critical Illness, Hospital coverage, A

Job summary

Abbott in Portland, OR is seeking an Inspector, Quality Control for a 12-month, 100% onsite assignment. The role focuses on visual and physical inspections of materials and products, ensuring adherence to quality specs and GDP/FDA regulations.

The incumbent will maintain records, manage NCRs, and support process improvements with production and engineering teams. Requirements include a high school diploma or equivalent (technical degree preferred) and 1+ years in manufacturing quality roles.

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/quality role is desired.

Responsibilities

  • Inspect and test raw materials, in-process components and finished products to ensure quality.
  • Maintain Lot History Records, 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 perform routine maintenance on inspection/testing equipment.
  • Collaborate with production and engineering teams to drive quality improvements.

Skills

Attention to Detail
Communication
Documentation

Education

High school diploma or equivalent
Associate’s or Bachelor’s degree preferred

Tools

SAP
MS Excel
Outlook
Teams

Job description

Abbott in Portland, OR is seeking an Inspector, Quality Control for a 12-month, 100% onsite assignment. The role focuses on visual and physical inspections of materials and products, ensuring adherence to quality specs and GDP/FDA regulations.

The incumbent will maintain records, manage NCRs, and support process improvements with production and engineering teams. Requirements include a high school diploma or equivalent (technical degree preferred) and 1+ years in manufacturing quality roles.

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