Integra LifeSciences

Quality Assurance Technician

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


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.  Founded in 1989 Integra is headquartered in Plainsboro, New Jersey and has nearly 4,000 employees worldwide. Integra's common stock is listed on The NASDAQ Stock Market under the symbol "IART."


Integra LifeSciences has entered into an acquisition agreement of Codman Neurosurgery.   This transformational acquisition creates compelling value for our shareholders, employees and patients, and enhances our global position in neurosurgery by adding a complementary product portfolio and the world-recognized Codman brand. This expansion position is open as a result of this exciting acquisition.


Responsible for conducting technical quality assurance inspections and using results to improve production processes and standards.

  • Performs routine tests and analyses to assure that products comply with established specifications.
  • Carries out simple calculations and prepares documentation that shows the results of tests performed.
  • Program and validate inspection on CMM equipment.
  • Completes record of inspection results, acceptance, rejection and disposition for entry into log books or computer databases.
  • Sends test equipment for scheduled calibration and maintenance.
  • Assists with specialized product/customer quality testing and determine the conformity or not of a product linked to the specifications.
  • Assists with the implementation of revisions, corrections and changes to test equipment, procedures and methods.
  • Logs in defective products returned by customers to determine root causes of failure.
  • Train inspectors.
  • Gage R&R studies.
  • Observes discussions with quality, engineering and other relevant departments to learn about corrective actions for reoccurring problems.


  • Minimum of 0-2 years of related experience in a Quality Systems / Regulatory Compliance environment with a working knowledge preferably in the medical device, diagnostics or pharmaceutical industries
  • Familiarity with FDA regulations and ISO series of quality standards preferred
  • High School/Secondary Education or Equivalent
  • CFC in micromechanics, mechanics, or equivalent training or experience of technician in the field of mechanics or quality assurance.
  • Good knowledge of metrology, including a good knowledge of the measurment techniques of measures on CMM equipment
  • Knowledge of statistical tools (minitab)
  • Knowledge of the GMP
  • Knowledge of the GD&T

  • Fluent French and at least highly communicative English language skills


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