Integra LifeSciences

  • Sr. Manufacturing Engineer

    Vacancy ID
    2018-27406
    Location
    CA-ON-Tortonto
    Position Type
    Regular Full-Time
    Category
    Engineering
  • 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

    • Study and apply statistical methods to improve manufacturing and packaging processes, labour requirements and standard operating procedures.
    • Work with other teams in new product development, setup new packaging specifications and product cost
    • Perform productivity analysis through work measurements, time and motion studies, workplace design and minor improvements to ensure our costs and processes are in line with the competitive global market.
    • Participate, identify and implement continuous improvement projects
    • Create and maintain Bill of Materials on new and existing products (identify proper materials, labour standards, waste allowances, methodology/process, packaging specifications and cost.
    • Perform feasibility studies on capital investment, capacity studies, value analysis etc.
    • Identify, reduce and eliminate equipment breakdowns through correct preventative maintenance activities and failure cause elimination
    • Start transitioning to TPM working on equipment/process that cause the most downtime
    • Perform and execute, IQ and OQ requirements on new equipment or revalidations as well as support.
    • Evaluate machine/process requirements to minimize to eliminate cost of no-compliances, WIP etc.

     

    Qualifications

    • Bachelor's Degree in Engineering or equivalent
    • Minimum 7-10 years’ experience in related manufacturing industries
    • Working knowledge of cGMP, Clean Room procedures and ISO Quality Standards
    • Excellent Team building and developmental skills
    • Good communication and organization skills
    • Good analytical and problem solving skills
    • Good interpersonal skills & collaboration

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