What are the responsibilities and job description for the Engineer II, Engineering Development Program position at Terumo Neuro?
Job Description
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. These rotations include one (1) required rotation in Manufacturing Engineering and two (2) optional rotations from the following areas:
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:
US - United States
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. 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
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.
- Master’s degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Industrial Engineering, Chemistry, or other related discipline.
- Zero (0) to two (2) years of experience in medical devices, manufacturing and/or technical development.
- Demonstrated experience reading and preparing technical documentation.
- Knowledge of standard machine shop equipment and processes, and working knowledge of medical device manufacturing equipment and processes.
- Computer experience and skills including CAD and MS Office Suite (Word, Excel, Teams, Outlook, etc.).
- Strong analytical capability and organization skills.
- Strong interpersonal and verbal and written communication skills; the ability to work effectively in a team environment and autonomously.
- Knowledge of medical device materials and processes: adhesives, plastics/polymers, metals, laser-welding, laser-cutting, braiding, and lamination.
- SolidWorks or PRO/E proficiency (Preferred)
US - United States
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