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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 tests and inspects raw materials, work in process, and finished goods at various stages of production process.  Selects random samples for tests at specified stages such as incoming or in production process, and tests products for variety of qualities, such as dimensions, performance, appearance, correct assembly, and other testing instruments.  Records test data, applying statistical quality control procedures.

This is a 4th shift role. The 4th shift entitles 12 hour shifts Saturday and Sunday (5:00am-3:30pm), and two 8 hour shifts during the week assigned later when selected for the role. Therefore, the role requires full availability.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.

• Inspects labels, pid’s, and pouches visually to approve packing operations or other operations.
• Obtains samples, inspects samples to specifications, records inspection data and makes accept/reject decisions based on inspection findings with respect to specifications.
• Verifies dimensions, cavity measures, pressure and other specifications of products, using measuring gauges and testing equipment such as optical comparative, micrometers, calipers, go-no-go gauges, pin gauges, microscope, air pressure gauges, and other testing instruments.
• Follows quality control inspection criteria in order to release acceptable lots to store or reject lots to prior operations for re-work.
• Reads written specifications, drawings, and procedures such as the Quality Control Inspection Procedures.
• Fills quality control records, information on shop orders, and maintains other control reports and documentation.
• Assists in training of new Q.A. Inspectors.
• Provides G.M.P./Quality Manual reinforcement and conducts spot audits to manufacturing areas in order to assist production to achieve established goals.
• May be assigned to different workstations as product needs require.
• May use forklift or jack pallets for handling raw materials incoming inspection area.
• Sets up and performs destructive and non-destructive test on materials, parts or products to measure performance, material characteristics, etc.
• Maintains quality control records, blueprints, procedures, and other documentation's accurate, updated, and properly organized in files.
• Assures all control documentation are prepared and attached to the corresponding lots.
• Assures that all equipment’s are adequately calibrated and informs Supervisor of any discrepancy.
• Assures raw materials or products released to stores or for sterilization fulfill quality standards.
• Maintains work area clean and in orderly conditions.
• Follow Clean Room Rules and Gowning Practices.
• Must use safety shoes in areas that require it or the required protective equipment of the assigned workstation.  This applies to all area where safety shoes are required.
• Maintains control of raw material quarantine area and printed materials, and discrepant materials in store.
• Works on priority orders when released before others to assure compliance with production schedules.
• Assist the supervisor in any other duty as requested.

Minimum Qualifications:

• High School graduate or equivalent.
• One (1) year experience in a similar position in an FDA regulated manufacturing environment preferred.
• Driver’s license on heavy vehicles highly preferred.
• Knowledge of basic math concepts, graphs interpretation, and use of procedures, and inspection methods.
• Knowledge of statistical process control techniques.
• Ability to read, understand drawings and written documents in English.
• Ability to work using testing instruments and manual equipment.
• Ability to be in a standing position for long periods of time.

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.

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