Engineer II

Join to apply for the Engineer II role at Terumo Cardiovascular

At Terumo Cardiovascular, we develop, manufacture and distribute medical devices for cardiac and vascular surgery with an emphasis on cardiopulmonary bypass, intra‑operative monitoring and vascular grafting. This includes a full‑line of perfusion products, endoscopic vessel‑harvesting products and surgical‑stabilization products. Our mission is to work as a team to save one more life, today and every day. We do this by providing lifesaving technology to cardiac surgery teams around the world.

We’re working to build a healthier, happier society for our associates and the world. Our story begins over 100 years ago in Japan. Since then, we’ve been united by our mission to contribute to society through healthcare. As an associate at Terumo, your work helps shape our evolution for the future. Working as one team, learning, innovating and challenging ourselves to write the future of healthcare.

And no matter the location, no matter the team, we look out for one another, respect and support each other, strengthening trust with patients and healthcare providers everywhere.

This position is responsible for investigating, planning, and implementing improvements in and/or additions to current products and manufacturing processes that directly affect safety, quality, regulatory compliance, and productivity. The role may involve leading projects requiring multidisciplinary engineering effort.

• Demonstrate a primary commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all documented quality processes and procedures.
• Provide technical assistance to plan and implement specified projects, including organizing and leading projects across departments, planning and scheduling, coordinating resources, and preparing proper documentation.
• Assist with cause‑identification and problem‑resolution for various types of production or service‑related issues.
• Provide engineering input in the design, fabrication, development, installation, validation, and qualification of equipment and processes, including feasibility studies and proper documentation for justification of projects and training to ensure proper operation of equipment.
• Assist in planning and implementation of projects to develop, install, and qualify new processes for manufacturing new products or improving existing processes.
• Research and implement cost‑reduction projects.
• May assist in maintaining plant‑wide calibration system and drawing control/document control system.
• Gather, track, and analyze production data for meetings, business plans, and efficiencies.
• Plan work schedules, expenditures, attend meetings, and prepare monthly reports as required.
• Perform other duties as assigned.

Requires a four‑year college degree in an engineering, scientific, or technical discipline and a minimum of three years of experience in an engineering, scientific, or technical environment, or a Master’s degree in an engineering, scientific, or technical discipline and a minimum of two years of experience in an engineering, scientific, or technical environment. Basic computer software skills, i.e. Microsoft Office. Experience in medical device industry preferred.

• 401(k) with 6% matching
• Paid time off
• Company paid holidays
• Medical, dental, vision insurance
• Flexible spending account
• Health savings account
• Company paid life insurance
• Employee assistance program
• Parental leave
• Tuition reimbursement
• Onsite gym

Seniority level: Mid‑Senior level

Employment type: Full‑time

Industries: Motor Vehicle Manufacturing

Location: Ann Arbor, MI

Salary: $80,000–$210,000