R&D Sustaining Engineering Intern — IVUS Medical Devices

Boston Scientific; Maple Grove (MN); On-site; USD 43,000 - 74,000; Full time

Job summary

Boston Scientific is offering an on-site Sustaining R&D Internship in Maple Grove, MN, focused on optimizing and sustaining commercial IVUS products used in interventional cardiology. You will support design improvement and supply continuity while building relationships across diverse engineering teams.

The role emphasizes design change activities, investigations, and compliant documentation, with opportunities to develop in a global medical technology leader over a structured summer program.

Qualifications

• Must graduate between Fall 2027 and Spring 2028.
• Pursuing a degree in Biomedical, Mechanical Engineering, or Chemical Engineering.
• Eligible to work in the U.S. without company sponsorship (now or in the future).
• Reliable transportation to Maple Grove, MN (Arbor Lakes) location.

Responsibilities

• Design and Testing: assist in design change activities to improve or maintain supply of commercial products, including feasibility studies and product testing.
• Problem-Solving and Compliance: support investigations into failure modes, perform root cause analyses, and develop solutions; ensure regulatory compliance.
• Cross-Functional Collaboration: work with project management, marketing, design assurance, manufacturing, and regulatory affairs to ensure project success.
• Documentation and Reporting: prepare and review engineering documents, design change analysis, DHF, and regulatory submissions.

Skills

Problem solving

Communication

Time management

Education

Biomedical Engineering

Mechanical Engineering

Chemical Engineering

Job description

Boston Scientific is offering an on-site Sustaining R&D Internship in Maple Grove, MN, focused on optimizing and sustaining commercial IVUS products used in interventional cardiology. You will support design improvement and supply continuity while building relationships across diverse engineering teams.

The role emphasizes design change activities, investigations, and compliant documentation, with opportunities to develop in a global medical technology leader over a structured summer program.