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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.

The Quality Inspector is responsible for product and material inspections, verifications, and checks.  The Quality Inspector shall ensure documentation is complete and accurate, release material physically and electronically, and maintain quarantine areas.

Responsibilities:

Performs all incoming inspections and testing of materials and components, for in-process functional testing and verifications, and for quality control of instruments as applicable

Performs QC testing/ inspections/verifications on manufacturing supplies, in-process materials, and finished products as necessary

Performs label inspection and verification, as applicable

Enters inspection results into appropriate software database

Reviews incoming inspection records on components to ensure compliance to product specifications

Maintains strict control of quarantine areas in an organized manner

Participates in RMA (Return Material Authorization) inspection activities, as applicable

Coordinates supply orders for inspection activities with QC Management

Report non-conforming product to QC Management

Works in a Team environment to coordinate job duties

Performs environmental monitoring in controlled areas 

Performs weekly water sampling

Performs product discard and destruction activities, as needed

Maintains product retains, as applicable

Perform other related duties as assigned and delegated by Quality Control Management

The employee must be able to work in a cleanroom environment.

Qualifications:

High School Diploma or equivalent

Experience in medical devices, pharmaceuticals, or other regulated industry preferred.

Ability to assess results against acceptance criteria.

Ability to follow instructions precisely, recognize deviations, and recommend corrective action.

Working knowledge of current Good Manufacturing Practices.

Familiarity with application of FDA and ISO quality standards in a government regulated industry.

Proficient computer skills, including experience with database applications and Microsoft Office.

Working knowledge of standard laboratory practices and safety.

Detail-oriented.

Excellent organizational and time management skills.

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.

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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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