QA Inspector I - Medical Devices | Impact & Growth

Integra LifeSciences; West Valley City (UT); On-site; USD 23,419 - 30,307; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Short-term disability

Long-term disability

401(k)

Job summary

Integra LifeSciences in West Valley City, Utah seeks a Quality Inspector to verify raw materials, in-process assemblies, and finished goods against ISO 13485, FDA 21 CFR 820, and GMP standards.

You will maintain GDP-compliant records, support root-cause analysis, and collaborate with Quality Engineers and Production teams to resolve issues while upholding a safe, clean work environment. The role offers competitive hourly pay and comprehensive benefits.

Qualifications

• 1–5 years of experience in quality inspection or a similar role within the medical device, pharmaceutical, or regulated manufacturing industry.
• Familiarity with ISO 13485, FDA 21 CFR 820, and Good Manufacturing Practices (GMP) is preferred.

Responsibilities

• Conduct incoming inspections of raw materials and components to verify compliance with specifications.
• Perform in-process inspections to ensure assemblies meet quality and regulatory standards.
• Inspect finished goods returning from sterilization to ensure compliance with final release criteria.
• Verify labels and packaging for accuracy and compliance with regulatory requirements.
• Ensure assembly instructions are properly followed by reviewing Lot History Records.
• Identify and document nonconformities through the Nonconforming Material Reports (NCMR) process.
• Work collaboratively with Quality Engineers and Production teams to resolve quality issues.
• Maintain complete and accurate inspection records in compliance with Good Documentation Practices (GDP).
• Support continuous improvement initiatives and participate in root cause analysis and corrective actions.
• Maintain a clean and safe working environment in accordance with company policies.
• Perform other related duties as required.

Skills

Inspection techniques

Reading drawings

Attention to detail

MS Office

eQMS

Cross-functional collaboration

Education

Equivalent combination of education and experience

Job description

Integra LifeSciences in West Valley City, Utah seeks a Quality Inspector to verify raw materials, in-process assemblies, and finished goods against ISO 13485, FDA 21 CFR 820, and GMP standards.

You will maintain GDP-compliant records, support root-cause analysis, and collaborate with Quality Engineers and Production teams to resolve issues while upholding a safe, clean work environment. The role offers competitive hourly pay and comprehensive benefits.