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

To perform this job successfully, an individual must be able to execute the following responsibilities satisfactorily:

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.

Desired Minimum Qualifications

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.

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 careers@integralife.com or call us at 855-936-2666.

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