QA Inspector I: Precision in Medical Devices

INTEGRA LIFESCIENCES CORP

West Valley (WA)

On-site

USD 23,419 - 30,307

Full time

14 days+
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
401(k) plan
Disability insurance

Job summary

Integra LifeSciences is seeking a Quality Inspector on site in the United States. Responsibilities include inspecting raw materials, in-process assemblies, and finished goods to ensure compliance with ISO 13485, FDA 21 CFR 820, and GMP standards.

The role emphasizes accurate documentation, lot-history review, and participation in corrective actions. The ideal candidate has 1–5 years of experience in regulated manufacturing, strong attention to detail, and proficiency with MS Office and eQMS

Qualifications

  • 1–5 years of quality inspection experience in medical device or regulated manufacturing.

Responsibilities

  • Perform incoming inspections of raw materials and components.
  • Inspect in-process assemblies for quality and regulatory compliance.
  • Verify finished goods from sterilization meet release criteria.
  • Review lot histories to ensure assembly instructions followed.
  • Document nonconformities via the NCMR process.
  • Collaborate with Quality Engineers and Production to resolve issues.
  • Maintain GDP-compliant inspection records.
  • Support root cause analysis and corrective actions.
  • Maintain a clean and safe work environment.
  • Perform other related duties as required.

Skills

Inspection techniques
Drawings interpretation
Documentation
MS Office & eQMS
Communication

Job description

Integra LifeSciences is seeking a Quality Inspector on site in the United States. Responsibilities include inspecting raw materials, in-process assemblies, and finished goods to ensure compliance with ISO 13485, FDA 21 CFR 820, and GMP standards.

The role emphasizes accurate documentation, lot-history review, and participation in corrective actions. The ideal candidate has 1–5 years of experience in regulated manufacturing, strong attention to detail, and proficiency with MS Office and eQMS

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