R&D Engineer III - Intravascular Lithotripsy

Skip to main contentDashboardProfileJoin Talent NetworkSign InEnglishSingle PositionView All JobsR&D Engineer III - Intravascular LithotripsyMaple Grove US-MN, United States | N/A No longer accepting applications.Work ModeOnsiteRequisition ID630598Additional Location(s):  N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.           About the role:We are excited to offer a unique opportunity for an R&D Engineer III to join our team, supporting Acquisition Integration in the Interventional Cardiology and Vascular Therapies division at Boston Scientific. This role will support the integration and development of Intravascular Lithotripsy technologies to treat calcified artery disease, with a focus on design and quality system integration. You will gain exposure to the full product development process (PDP) in a fast-paced, collaborative environment.Job Description and Responsibilities:The R&D Engineer III will contribute to integration-focused development and design activities. This role requires solid technical fundamentals, working knowledge of design controls and risk management execution, and the ability to perform a range of assignments with a moderate level of guidance while collaborating with cross-functional partners to deliver high-quality product solutions.Integration Execution: Support acquisition integration workstreams to incorporate new technologies into Boston Scientific systems and processes; contribute to interface definition, requirements alignment, integration planning, and technical decision-making for assigned deliverables.Design Controls & Quality System Execution: Develop and deliver design control outputs (user needs, design inputs/outputs, traceability, risk management, verification/validation, and DHF documentation) in accordance 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 implement solutions to technical and quality challenges; identify integration risks and support 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 support successful integration execution, timely deliverables, and clear communication of technical information.Required qualifications:BS or above in Mechanical Engineering, Biomedical Engineering, or related field4+ years of engineering experience with a Bachelor’s degree or 2+ years with an advanced  degree2+ years of experience with Medtech device design and development in a design controls environmentExperience with catheter and/or single-use medical device design and developmentWorking knowledge of design controls, risk management, and documentation (e.g., requirements, traceability, verification/validation, DHF, change control)Strong technical knowledge, problem-solving abilities, collaborative mindset, and effective communication skills; able to exercise judgment using practical experience and prescribed guidelinesAbility to travel up to 15%Preferred qualifications:Previous experience with product acquisition integration and/or technology/platform integrationPersonal drive, individual accountability, and a strong bias for action; independent critical thinker with willingness to...