IQA Technician II: Precision Inspector for Medical Devices

Experis Technology Group

Atlanta (GA)

On-site

USD 30,000 - 36,000

Full time

7 days ago
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Benefits offered by this job

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

Job summary

ManpowerGroup's Experis division in Atlanta is seeking an IQA Technician II to support GMP/GLP-compliant inspections for complex medical devices. The role includes tier 1/2 inspections, use of advanced measurement tools, and documentation of non-conformances.

Ideal candidates have a high school diploma, 2–5 years of quality inspection experience, and knowledge of FDA, GMP, and ISO 13485, plus proficiency with Word and Excel. On-site with comprehensive benefits.

Qualifications

  • High School Diploma or GED required.
  • 2-5 years experience in quality inspections.
  • Experience with measurement equipment, hand tools, gauges.
  • Training in blueprint reading and inspection sampling techniques.
  • Knowledge of FDA, GMP, and ISO 13485; strong communication and computer skills (Word and Excel).

Responsibilities

  • Perform tier 1 & 2 inspections of inbound material and test equipment.
  • Document non-conformances and configure corrective actions.
  • Review sampling plans and drawings, interpret measurement methods.
  • Support troubleshooting and continuous quality improvement.

Skills

Quality inspections
FDA knowledge
GMP
ISO 13485
Blueprint reading
Inspection sampling
Communication skills
Microsoft Word
Excel

Education

High School Diploma or GED

Tools

Measurement equipment
Hand tools
Gages
Pressure testing
Force gage testing

Job description

ManpowerGroup's Experis division in Atlanta is seeking an IQA Technician II to support GMP/GLP-compliant inspections for complex medical devices. The role includes tier 1/2 inspections, use of advanced measurement tools, and documentation of non-conformances.

Ideal candidates have a high school diploma, 2–5 years of quality inspection experience, and knowledge of FDA, GMP, and ISO 13485, plus proficiency with Word and Excel. On-site with comprehensive benefits.

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