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Senior R&D Engineer - Intravascular Lithotripsy

Job in Maple Grove, Hennepin County, Minnesota, 55311, USA
Listing for: B Capital
Full Time position
Listed on 2026-07-09
Job specializations:
  • Engineering
    Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 85000 - 161500 USD Yearly USD 85000.00 161500.00 YEAR
Job Description & How to Apply Below

Additional Location(s): N/A

Diversity
- Innovation
- Caring
- Global Collaboration
- Winning Spirit
- High Performance

Boston Scientific is a global medical technology leader that advances science to improve the health of patients worldwide. We provide high‑performance solutions across cardiovascular, respiratory, digestive, oncological, neurological and urological disease areas.

About the role

We are excited to offer a unique opportunity for a Senior R&D Engineer to join our team, supporting Acquisition Integration in the Interventional Cardiology and Vascular Therapies division. The role focuses on integrating and developing Intravascular Lithotripsy technologies for the treatment of calcified artery disease, with a strong emphasis on design and quality system integration. You will work through the full product development process (PDP) in a fast‑paced, collaborative environment.

Job Description and Responsibilities

The Senior R&D Engineer will contribute to and lead integration‑focused development and design activities. This role requires technical depth, strong design controls and risk management execution, and the ability to operate independently while influencing cross‑functional partners to deliver high‑quality product solutions.

  • Integration Leadership:
    Own and lead integration work streams to incorporate new technologies into Boston Scientific systems and processes; drive interface definition, requirements alignment, integration planning, and technical decision‑making.
  • Design Controls & Quality System Ownership:
    Lead and deliver design control outputs (user needs, design inputs/outputs, traceability, risk management, verification/validation, and DHF documentation) to ensure compliance with relevant standards, regulations, and internal procedures.
  • Design and Development:
    Conduct feasibility studies, develop prototypes, and plan/execute testing to optimize product designs and support integration readiness across multiple device models and iterations.
  • Problem‑Solving and Compliance:
    Investigate failure modes, perform root cause analyses, and develop solutions to technical and quality challenges; proactively identify integration risks and drive mitigation plans with cross‑functional partners.
  • Cross‑Functional

    Collaboration:

    Work closely with cross‑functional and multi‑site teams, including quality, manufacturing, supplier engineering, and regulatory affairs, to ensure successful integration execution, timely deliverables, and clear communication of complex technical information.
Required qualifications
  • BS or above in Mechanical Engineering, Biomedical Engineering, Materials Science, or equivalent.
  • 6+ years of engineering experience with a Bachelor’s degree; 4+ years with a Master’s degree; or 2+ years with a PhD.
  • Experience with catheter and/or single‑use medical device design and development.
  • Working knowledge of design controls, risk management, and documentation (e.g., requirements, traceability, verification/validation, DHF, change control).
  • Demonstrated ability to lead work streams, manage tasks to completion, and influence cross‑functional partners without authority.
  • Strong technical problem‑solving and communication skills; able to work independently while receiving guidance on complex and unprecedented problems.
  • Ability to travel up to 15%.
Preferred qualifications
  • Previous experience with product acquisition integration and/or technology/platform integration.
  • Personal drive, individual accountability, and a strong bias for action; independent critical thinker with willingness to challenge the status quo.
  • Comfortable working in ambiguity; adaptable and agile in response to evolving priorities.
  • Hands‑on experience with balloon catheter and/or catheter system product development for single‑use devices.
  • Test method development experience.
  • Class II or Class III medical device product development experience and regulatory requirements.
  • Familiarity with Boston Scientific quality systems or similar industry standards.

Requisition

Minimum Salary: $ 85000

Maximum Salary: $ 161500

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) will vary based…

Position Requirements
10+ Years work experience
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