Quality Assurance Inspector

Quality Assurance Inspector I is responsible for performing in‑process and final inspections to ensure compliance with established quality standards and regulatory requirements for medical devices. The role supports the development, implementation, and monitoring of quality programs to ensure compliance with ISO 13485, FDA regulations (21 CFR 820), and other applicable industry standards.

• 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 regulatory compliance.
• Ensure assembly instructions are properly followed by reviewing Lot History Records.
• Identify and document nonconformities through the Nonconforming Material Reports (NCMR) process.
• Collaborate 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.

• 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.

• 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 electronic quality management systems (eQMS).
• Effective communication and collaboration skills to work across departments.

$16.68 – $22.12 USD hourly. Pay is determined by role, level, and location, and may be affected by experience and education.

• Medical, dental, vision, and life insurance.
• Short‑term and long‑term disability, business accident, and group legal insurance.
• 401(k) savings plan.

Integra Life Sciences 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 by applicable U.S. laws and governmental regulations. For more information on rights under the law, see https://(Use the "Apply for this Job" box below).

and https:// Integra Life Sciences provides reasonable accommodations for qualified applicants and employees with disabilities in accordance with the ADA. Accommodations can be requested by emailing