Integra LifeSciences

  • Senior Quality Engineer

    Vacancy ID
    CH-NE-Le Locle
    Position Type
    Regular Full-Time
    Quality Assurance
  • Overview

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    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."


    Currently we are looking for Senior Quality Engineer for a 1-year fix term conract with an extention option.



    • Plan, coordinate and direct the quality aspects of process validations
    • Write validation tests and reports (IQ, OQ, PQ, PPQ)
    • Issue validation documentation (including protocols and completion reports, process specifications, work instructions, etc…), coordinate activities to their execution and analyze resulting data
    • Provide support for Quality Control, Operations and Quality System.
    • Quality & Process improvement project support
    • Approves changes to documentation and processes
    • Management and follow-up of non-conformities and corrective actions
    • Provide project updates and presentations to all level of the organization
    • Ensure activities are carried out according to appropriate internal and external standards for Health, Safety & Environment, Regulatory (GMP, ISO; FDA, internal policies) and Quality system
    • Maintain project documentation and suggest improvements to systems and procedures
    • Performs other related functions as required


    Education / Experience:

    • Engineer level or equivalent
    • 2-8 years of experience in a similar function
    • Fluent in French and English



    • Experienced in Quality
    • Medical &/or Pharmaceutical industry knowledge
    • Experienced in micro-mechanism assembly process: molding, welding, gluing, press fitting
    • Proactive, rigorous, creative & taking initiative
    • Technical and analytical skills.
    • Medical standards knowledge (ISO & FDA)
    • Well organized and result oriented
    • Autonomous with attention to details
    • Ability to work with cross functional team (R&D, Manufacturing Engineering, Procurement, Manufacturing, HSE)
    • Ability to travel abroad occasionally
    • Office tools


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