Boston Scientific
R&D Engineer Ii
This is a key opportunity in R&D for ICTx within the BSC's Cardiology division. ICTx continues to be an exciting growth driver for BSC. The ideal candidate will demonstrate a blend of technical knowledge, leadership, collaborative teamwork, and diligent experimentation. This role will serve as an Extended Team Member/Workstream Lead to develop next-generation products so BSC can deliver life-changing medical devices to patients and clinicians in support of BSC's mission. Please note: This role requires up to 25% travel to Carlsbad, CA or temporary relocation to Carlsbad, CA for a period of 6 months. Boston Scientific will provide support for relocation and temporary living expenses. At the conclusion of the temporary assignment, the role will be returned to Maple Grove, MN. Please apply only if you're comfortable with this arrangement. Work mode: Hybrid Onsite Location(s): Maple Grove, MN, US, 55311 Additional Location(s): N/A Your responsibilities will include: Assist in all aspects of design control for the full product portfolio. Leading the design & execution of structured experimental plans to drive data-based decisions. Drive test method development and validation activities. Facilitating crisp decision making around key technical issues for your workstreams. Understanding clinical use cases and user interface requirements to drive design decisions. Working cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing to ensure project success. Provide multiple options and considerations based on feedback from clinical, manufacturing and business teams. Training and/or provide work direction to technicians and other engineers. Documenting development by writing documents, reports, memos, change requests. Solving engineering problems by analyzing the situation and recommending solutions or alternative actions. In all actions, demonstrating a primary commitment to patient safety and product quality by maintaining compliance to all documented quality processes and procedures. Required qualifications: BS in Mechanical Engineering, Biomedical Engineering, or related field. 2+ years of experience with bachelors, or 1+ years with a master's degree. Strong hypothesis-driven experimental design, problem solving and statistical analysis skills. Ability to draw conclusions and make recommendations based on technical inputs from multiple and varied sources. Candidates should have a high sense of urgency, be self-starters and have a hands-on approach. Must work Onsite at our Maple Grove, MN location. Preferred qualifications: Bachelor's degree in mechanical or biomedical engineering preferred. Proficient in designing products, components, assemblies, and/or fixturing utilizing SolidWorks. Experience with medical device development for single use devices and those containing Electronic Medical Equipment. Experience with drafting and maintaining DHF and DMR documentation. Ability to build strong relationships across the organization. Experience in driving technical trade-off decisions to optimize design, performance, usability, manufacturability, cost-efficiency and reliability. Strong written and verbal communication, judgment, decision-making, and critical thinking skills.
This is a key opportunity in R&D for ICTx within the BSC's Cardiology division. ICTx continues to be an exciting growth driver for BSC. The ideal candidate will demonstrate a blend of technical knowledge, leadership, collaborative teamwork, and diligent experimentation. This role will serve as an Extended Team Member/Workstream Lead to develop next-generation products so BSC can deliver life-changing medical devices to patients and clinicians in support of BSC's mission. Please note: This role requires up to 25% travel to Carlsbad, CA or temporary relocation to Carlsbad, CA for a period of 6 months. Boston Scientific will provide support for relocation and temporary living expenses. At the conclusion of the temporary assignment, the role will be returned to Maple Grove, MN. Please apply only if you're comfortable with this arrangement. Work mode: Hybrid Onsite Location(s): Maple Grove, MN, US, 55311 Additional Location(s): N/A Your responsibilities will include: Assist in all aspects of design control for the full product portfolio. Leading the design & execution of structured experimental plans to drive data-based decisions. Drive test method development and validation activities. Facilitating crisp decision making around key technical issues for your workstreams. Understanding clinical use cases and user interface requirements to drive design decisions. Working cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing to ensure project success. Provide multiple options and considerations based on feedback from clinical, manufacturing and business teams. Training and/or provide work direction to technicians and other engineers. Documenting development by writing documents, reports, memos, change requests. Solving engineering problems by analyzing the situation and recommending solutions or alternative actions. In all actions, demonstrating a primary commitment to patient safety and product quality by maintaining compliance to all documented quality processes and procedures. Required qualifications: BS in Mechanical Engineering, Biomedical Engineering, or related field. 2+ years of experience with bachelors, or 1+ years with a master's degree. Strong hypothesis-driven experimental design, problem solving and statistical analysis skills. Ability to draw conclusions and make recommendations based on technical inputs from multiple and varied sources. Candidates should have a high sense of urgency, be self-starters and have a hands-on approach. Must work Onsite at our Maple Grove, MN location. Preferred qualifications: Bachelor's degree in mechanical or biomedical engineering preferred. Proficient in designing products, components, assemblies, and/or fixturing utilizing SolidWorks. Experience with medical device development for single use devices and those containing Electronic Medical Equipment. Experience with drafting and maintaining DHF and DMR documentation. Ability to build strong relationships across the organization. Experience in driving technical trade-off decisions to optimize design, performance, usability, manufacturability, cost-efficiency and reliability. Strong written and verbal communication, judgment, decision-making, and critical thinking skills.