Position Overview

This 18-month rotational program is designed to train new Engineers on various aspects of MicroVention Terumo technology, procedures, and processes. All candidates will be assigned a Mentor, Peer Mentor, as well as an Advisor to oversee their program succession, and will be provided with additional classroom training. Successful candidates will have three (3) six-month rotations. Assignments within a rotation will be clearly defined objectives within 3-month increments. These rotations include one (1) required rotation in Manufacturing Engineering and two (2) optional rotations from the following areas:
  • Research & Development (R&D)
  • Equipment/Tool Design
  • Marketing
  • Regulatory Affairs
  • Quality
  • Supply Chain
Job duties:
Support development of medical device products with work including writing or verifying specifications, designing new products, fixtures, test processes, equipment and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Typical job duties might include:
  • Developing new product concepts and products.
  • Engineering design and process development.
  • Generating intellectual property and writing invention disclosures.
  • Supervising assemblers, technicians, and specialists.
  • Largely self-directed, capable of meeting project goals with moderate supervision.
  • Perform additional duties as assigned.

    1. Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Industrial Engineering, Chemistry, or other related discipline.
    2. Zero (0) to two (2) years of experience in medical devices, manufacturing and/or technical development.
    3. Demonstrated experience reading and preparing technical documentation.
    4. Knowledge of standard machine shop equipment and processes, and working knowledge of medical device manufacturing equipment and processes.
    5. Computer experience and skills including CAD and MS Office Suite (Word, Excel, Teams, Outlook, etc.).
    6. Strong analytical capability and organization skills.
    7. Strong interpersonal and written and verbal communication skills; the ability to work effectively in a team environment and autonomously.
    8. Knowledge of medical device materials and processes: adhesives, plastics/polymers, metals, laser-welding, laser-cutting, braiding, and lamination.
    Desired Qualifications
    1. SolidWorks or PRO/E proficiency (preferred).
    Engineer II Requirements:
    1. Master’s degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Industrial Engineering, Chemistry, or other related discipline
    2. Zero (0) to two (2) years of experience in medical devices, manufacturing and/or technical development
    3. Demonstrated experience reading and preparing technical documentation
    4. Knowledge of standard machine shop equipment and processes, and working knowledge of medical device manufacturing equipment and processes
    5. Computer experience and skills including CAD and MS Office Suite (Word, Excel, Teams, Outlook, etc.)
    6. Strong analytical capability and organization skills
    7. Strong interpersonal and verbal and written communication skills; the ability to work effectively in a team environment and autonomously
    8. Knowledge of medical device materials and processes: adhesives, plastics/polymers, metals, laser-welding, laser-cutting, braiding, and lamination