Position Overview

Are you interested in working for an organization that is making a difference in people’s lives every day? We’re a medical devices company that develops innovative neuroendovascular technologies for the treatment of vascular disease. We’re a high-growth, customer-focused company with an entrepreneurial spirit producing some of the most reliable and technologically advanced products supported by proven clinical data. Take a closer look at what MicroVention® TERUMO has to offer.

Maintain the database and provide training materials for all Quality Control associates. Maintain training records in accordance with the quality system as established by the company. Job duties:
  • Ability to prepare training materials and accurately maintain control of pending training to be completed by Quality Inspectors.
  • Maintain training records per GMP, GDP and quality system requirements.
  • Coordinate training between QC Inspectors and initiators.
  • Coordinate and execute effective trainings when changes are done in Product Drawings (PD), Build Records (BR), Quality Specifications (QS) and Test Methods (TM), etc.
  • Coordinate activities cover by WI6.2.4 and make sure trainings are complete on time.
  • Assist with providing updated released controlled copies for QC Inspectors stations use.
  • Keep training Matrix (CF12099) and training files up to date.
  • Keep training plan and and log for product QC Inspectors (CF388) up to date.
  • Coordinate re-certification activities with Engineers (if needed).
  • Perform internal audits to training files to assure they are updated and in compliance.
  • Support Engineers, supervisors and leader on investigations related to training activities and look for evidence, when needed.
  • Perform other duties as assigned.
    1. Minimum three (3) years of experience in quality control environment.
    2. One (1) year experience in medical device industry.
    3. High School Diploma or equivalent.
    4. Must possess good communication skills and with the ability to communicate professionally with internal and external customers.
    5. Ability to read, comprehend and follow company procedures as written.
    6. Intermediate computer skills and knowledge of MS Office, Outlook and Excel required.
    7. Ability to work with moderate supervision.
    8. Experience to navigation of computer-based training.
    Desired Qualifications
    1. Knowledge of medical device document control requirements and practices a plus.
    2. Be proactive, analytical, and organized.
    3. Able to follow company procedures and be a role model.
    4. Equipment use experience, like microscopes, rulers, video systems, etc. and able to understand product drawings, this will help to execute training needed.