Quality Assurance Inspector I

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

Changing lives. Building Careers.

Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.

Key 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.

Education & Experience

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

Skills & Competencies

• Strong knowledge of inspection techniques, measurement tools, and quality control methods.
• Ability to interpret technical drawings, specifications, and work instructions.
• Excellent attention to detail and documentation skills.
• Proficiency in Microsoft Office (Excel, Word, Outlook) and ability to use electronic quality management systems (eQMS).
• Effective communication and collaboration skills to work across departments.

Salary Pay Range

$16.68 - $22.12 USD Hourly

Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job‑related skills, experience, and relevant education or training.

Benefits

Employees and eligible dependents are eligible to participate in the following company‑sponsored benefit programs: medical, dental, vision, life insurance, short‑ and long‑term disability, business accident insurance, group legal insurance, and a savings plan (401(k)).

EEO Statement

Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.

This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices: EEO Is the Law | EOE including Disability/Protected Veterans.

Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at [e-mail].