Integra LifeSciences

  • Staff Engineer

    Vacancy ID
    CH-NE-Le Locle
    Position Type
    Regular Full-Time
  • 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 3,300 employees worldwide. Integra's common stock is listed on The NASDAQ Stock Market under the symbol "IART."


    • Lead production cells from the manufacturing engineering function.
    • Provide engineering input to solve complex manufacturing process and product design problems in the medical assembly environment to achieve cost effective solutions in a timely manner.
    • Provide production support updates and presentations to all level of the organization.
    • Participate actively to cross-functional team for project deployment.
    • Provide production support technical inputs to plan, design, develop and validate manufacturing processes.
    • Lead technical investigations and feasibility studies as required.
    • Design, develop and implement equipment and tooling; execute associated installation qualification and validation activities.
    • Provide technical information on appropriate areas to all functions within the business.
    • 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 production support documentation and suggest improvements to systems and procedures.
    • Apply project management methodology to deliver equipment and products implementation.


    • Thorough knowledge of the validation requirement of Medical Devices
    • Experience within medical device manufacturing industry is appreciated
    • Process improvement methodologies
    • Knowledge of Process Excellence methodologies (Lean Manufacturing, Six Sigma) is an asset
    • Knowledge of 3D CAD system (NX or equivalent) is a plus
    • Knowledge of 3D dimensioning and measurement
    • Knowledge of enterprise systems (ERP / PLM / Quality system)
    • Well organized and result oriented
    • Autonomous with attention to details
    • Ability to work with cross functional team (R&D, Quality Engineering, Procurement, Manufacturing, HSE)
    • Good communication skills; making complex issue easy to understand for others, ability to prepare communication for all level of the organization
    • Ability to travel abroad occasionally
    • Office tools
    • Engineering degree in mechanics / micromechanics
    • 5-15 years of relevant work experience, demonstrating valuable impact on business.
    • Fluent in French and English


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