Integra LifeSciences

  • QA Laboratory Technician

    Vacancy ID
    2018-26919
    Location
    CH-NE-Le Locle
    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

    Responsibilities: 

    • Water, Gazes, Environmental Sampling
    • Reception and preparation of sample labels
    • Endotoxin, Bioburden and H.P.L.C analyses of routine samples using test methods.
    • Logging samples into electronic lab systems (Empower3, WinKQCL, SAP and Carl Master) or manual systems which would include logbooks and the maintenance of control numbers.
    • Identification problems during the analysis and respect of process deviation / Non-conformity
    • Performing daily calibration / revalidation/ verification checks on laboratory instruments.
    • Making and recording lab observations and calculations.
    • Review and approve laboratory analyses.
    • Archiving documentation on testing that has been completed.
    • Performing other related duties as assigned by management.
    • Maintaining 5S, EHS level and clean work area.
    • Supporting laboratory housekeeping, environmental and safety initiatives.
    • Promote and nurture the highest standards of professionalism, ethics and compliance.

    Qualifications

    Requirements: 

    • An Associate’s degree, High School Diploma or Equivalent is required.
    • 5-10 years of experience in a GMP laboratory environment performing progressively duties.
    • Must be able to interact well with peers and colleagues
    • Technical on Microbiology / Biochemistry analyses and sterility assurance knowledge
    • Training in GMP and ISO requirements.
    • Ability to communicate in writing and orally.
    • Strong teamwork and communication skills to work effectively on cross-functional project teams, interacting with a diversity of disciplines.
    • Know and follow all laws and policies that apply to the position, and maintain the highest levels of professionalism, ethics and compliance
    • Good interpersonal and organizational skills.
    • Problem-solving and continuous improvement oriented.
    • Self-motivated

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