Integra LifeSciences

  • Manager, Quality Assurance Training

    Vacancy ID
    2018-26699
    Location
    US-NJ-Plainsboro
    Position Type
    Regular Full-Time
    Category
    Quality Assurance
  • 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 4,500 employees worldwide. Integra's common stock is listed on The NASDAQ Stock Market under the symbol "IART."

    Responsibilities

     

    • Develop and maintain quality system training requirements, including identification of external training/qualifications as necessary by function (e.g. professional organizations or accreditation programs; such RAB, ASQ, RAC).
    • Design education programs for general QA/RA training and specific elements of Quality Systems and Regulatory Compliance.
    • Identify and manage external resource(s) to support training and education curricula development as required.
    • Identify best practices and process improvements for training identification, implementation, completion, and methods for evaluating training effectiveness.
    • Develop and implement improved processes. Identify opportunities to streamline and further automate software/systems solutions.
    • Evaluate training curricula for sites and assist site personnel with the implementation of training programs and documentation practices.
    • Provide quarterly Management Review updates on the state of the Training and Education programs. Communicate expectations regarding training quality metrics and scores to all stakeholders and employees.

    Qualifications

    • Bachelors degree in Science or Education; Masters degree preferred
    • 7- 10 years experience in quality assurance or regulatory compliance in FDA regulated field
    • Minimum of 4 years experience in quality assurance training
    • Minimum of 3 years experience using automate software training solutions
    • Strong Medical Device background preferred
    • Experienced with evaluation, implementation and oversight of internal and external training programs
    • Knowledge of FDA regulations, ISO Standards and MOD laws/regulations
    • Excellent communication skills; experience facilitating training program required
    • Experience in Documentation Control and metrics analysis
    • Proficient in the use of Microsoft Office
    • Ability and willingness to travel

    Options

    Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
    Share on your newsfeed

    Need help finding the right job?

    We can recommend jobs specifically for you! Click here to get started.