Integra LifeSciences

  • Sr. Quality Inspector

    Vacancy ID
    2018-26407
    Location
    US-TX-Austin
    Position Type
    Regular Full-Time
    Category
    Manufacturing
  • Overview

    Integra LifeSciences, a world leader in medical technology, is dedicated to limiting uncertainty for surgeons, so they can concentrate on providing the best patient care. Integra offers innovative solutions in orthopedic extremity surgery, neurosurgery, reconstructive and general surgery, and regenerative wound care.

     

    Integra's orthopedic products include devices and implants for foot and ankle, hand and wrist, shoulder and elbow, tendon and peripheral nerve protection and repair. Integra is a leader in neurosurgery, offering a broad portfolio of implants, devices, instruments and systems used in neurosurgery, neuromonitoring, neurotrauma, and related critical care. Integra’s Tissue Technologies is an in-patient and outpatient Regenerative product portfolio, which includes products for wound care, burns, abdominal reconstruction, and plastic & reconstructive surgery. In the United States, Integra is a leading provider of surgical instruments to hospitals, surgery centers and alternate care sites, including physician and dental offices.

     

    Founded in 1989 Integra is headquartered in Plainsboro, New Jersey and has over 4,400 employees worldwide. Integra's common stock is listed on The NASDAQ Stock Market under the symbol "IART."

     

    It's a great time to join our growing company and become one of our impassioned colleagues making lives better for the patients we serve!

    Responsibilities

    • Completes all required quality inspections following inspection instructions and/or product drawings. Use department databases to track and manage inspection workload and rejected products.  Effectively follow SOPs, policies, and ISO/QSR requirements. 
    • Provides direction on inspection methods for Inspection Plan development or guidance to intermediate and entry level inspectors. Communicate technical details of materials to Engineers and other support staff accurately
    • Writes and processes Material Reject Reports, as necessary, and manage inventory that is on hold for quality inspection. Reviews and provides feedback inspection plans as needed. 
    • Provides support for the Quality System during corporate audits, actively participate in department activities and perform audits of operations areas to confirm compliance with controlled procedures, as required
    • Receive material coming into the building by suppliers, customers or other sources accurately and promptly, verifies the quantity and description of materials received by checking the merchandise against the packing list. Accurately place materials on shelves, in racks or other designated storage areas in an orderly manner.
    • Attaches identifying tag or labels to materials or marks information on cases, boxes or other containers. To accurately identify and count stock materials as listed on the cycle count/physical year-end inventory list.
    • Transact, receipts, shipments, movements, and work orders in a MRP system.

     

    Qualifications

    • High School or Trade School Graduate (or GED) minimum
    • Certified Quality Technician (ASQ CQT) would be a plus
    • Minimum 10 years’ experience in Quality Inspection (or minimum 12 years in a manufacturing environment with responsibility for measurement of products) and preferably in an FDA regulated environment. Prior experience with Medical Devices a plus.
    • Ability to develop and interpret instructions and drawings to effectively inspect product. Strong knowledge of GD&T preferred.
    • Ability to select and utilize multiple gauges and measurement tools for inspection of manufactured components and assemblies.
    • Previous experience with Optical Comparator and/or Vision System programming or operation preferred.
    • Use of math skills relative to physical measurement of product (calculations involving basic functions and some geometry/trigonometry in English and metric units)
    • Knowledge of ISO, FDA and QSR concepts and guidelines preferred.
    • Excellent communication and organizational skills.
    • Outstanding attention to detail
    • Strong interpersonal skills and ability to work with others in a positive and collaborative manner.
    • Ability to effectively communicate inspection methods and technical details to Engineers, Supervisors, and other inspectors in training.
    • Demonstrated ability to work accurately, follow instructions/schedules/timelines and handle multiple priorities.
    • Knowledge of various MS Office applications such as: Word, Outlook and Excel.
    • Experience using overlays to inspect also preferred.
    • Experience with Oracle preferred.
    • Experience with Agile preferred.

     

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