Principal Systems Engineer

Skip to main contentDashboardProfileJoin Talent NetworkSign InEnglishSingle PositionView All JobsPrincipal Systems EngineerValencia US-CA, United States | US-CA-ValenciaApply NowAdd to cartFind out how well you match with this jobUpload your resumeJob descriptionCompany and benefitsWork ModeHybridRequisition ID627934Additional Location(s): US-CA-ValenciaDiversity - 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:Boston Scientific was recognized by Forbes as one of the Best Workplaces for Engineers in 2026, reflecting a culture where engineers do meaningful work.As a Principal Systems Engineer on the Boston Scientific Neuromodulation R&D team, you will play a critical role in the design and development of complex medical systems from concept through product launch. This includes wearable, implantable, and connected cloud and mobile solutions that improve patient outcomes.In this role, you will lead system-level design efforts by translating user needs and stakeholder inputs into robust system requirements and architecture. You will guide cross-functional teams through implementation, integration, and verification activities across hardware, firmware, and software. This position requires strong technical leadership, systems thinking, and the ability to drive innovation in a highly regulated environment.At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Your responsibilities will include:Provide technical leadership across cross-functional engineering teams to deliver complex system solutions.Define, analyze, and manage system requirements, including clinical workflows, patient interactions, and input/output processes using systems engineering principles.Develop and document system architecture using industry-standard tools to model system interactions and dependencies.Apply critical thinking to identify and resolve system integration challenges, providing clear recommendations and solutions.Create and maintain design documentation, including requirements rationale, traceability, and system change analyses within the quality system.Partner with internal regulatory teams to develop reports and documentation supporting external regulatory submissions.Apply project management principles to plan, execute, track, and communicate progress across projects of varying scope and complexity.Support system risk management activities, including FMEA and hazard analysis, ensuring compliance with applicable standards.Required qualifications:Bachelor’s degree in biomedical engineering, electrical engineering, computer engineering, computer science, or a related field.Minimum of 12 years' experience in engineering; a master’s degree may substitute for 2 years of experience.Minimum of 10 years' experience working with mixed hardware and/or software systems.Minimum of 10 years' experience in the design, development, and testing in a regulated industry (medical systems and devices preferred).Demonstrated ability to develop and interpret system requirements and specifications.Preferred qualifications:Direct experience with therapy programming and delivery, patient alerts, and usability in wearable medical devices.Experience with neurostimulators and neuromodulation technologies.Experience working in an acquisition or integration environment.Familiarity with ecosystems involving wearable devices, mobile applications, and patient-facing user interfaces (UI/UX).Proven ability to work...