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Principal Software Engineer

Boston Scientific

Irvine, CA
Full Time
Senior
99k-188k
11 days ago

Job Description

About the Role

We are seeking an experienced and highly skilled Principal Software Engineer to join Boston Scientific Urology team. In this role, you will be part of evaluation, integration of software and firmware technologies for medical devices for Axonics/Boston Scientific Urology products. As a technical leader and hands-on contributor, you will lead integration activities and support software development, ensuring compliance with medical device regulations. This role requires experience with application software development, embedded systems, android platform, test frameworks, and regulatory-compliant medical device software development processes.

Key Responsibilities

  • Participate in technology evaluations, technical assessments and validation of software architectures, embedded software, and system integration aspects of acquired implantable medical devices.
  • Support software architecture, development, testing strategies and risk management activities for software applications.
  • Evaluate compliance and ensure software/firmware development aligns with IEC 62304, FDA, ISO 13485, ISO 14971 and other regulatory standards governing medical devices.
  • Oversee testing strategies (Unit/Integration) and design verification protocols to verify software/firmware functionality post-acquisition.
  • Support software/ firmware testing, debugging, and verification efforts using tools such as unit testing frameworks, hardware-in-the-loop (HIL) simulations, and automated test environments.
  • Identify potential risks, cybersecurity vulnerabilities, and integration challenges in acquired technologies. Ensure acquired software meets medical device cybersecurity and safety standards, including FDA premarket cybersecurity guidance, IEC 62443.
  • Collaborate with cross-functional teams, including hardware engineers, systems engineers, quality, regulatory affairs, manufacturing and PMO to ensure seamless device integration.
  • Establish and document software development lifecycle (SDLC) artifacts and processes to align with internal quality management systems (QMS). Maintain thorough design documentation, traceability matrices, and SDLC artifacts for regulatory submissions.
  • Provide technical inputs on low-power embedded systems, wireless communication (e.g., BLE, NFC, RF telemetry), and real-time operating systems (RTOS).
  • Act as a technical mentor for software engineers, guiding best practices during integration and new product software/firmware development.
  • Collaborate with regulatory teams on 510(k), PMA, or CE Mark submissions involving firmware-related changes.
  • Foster a culture of innovation, continuous improvement, and knowledge sharing within the R&D team.

Requirements

  • B.S or higher in Computer Science, Electrical Engineering, Computer Engineering, Software Engineering or related major.
  • 5+ years of experience in software development (Master's degree may substitute for one year of experience).
  • 3+ years in embedded or application software for medical devices.
  • Sound knowledge of software engineering principles and practices.
  • Knowledge of programming languages such as Swift, Java, Dart, or Objective-C and mobile operating systems and platforms such as iOS and Android.
  • Experience in developing mobile applications in an FDA regulated environment or other regulated industry.
  • Strong C/C++ skills for programming microcontroller systems.
  • Knowledge and use of OOP design principles, API design principles.
  • Knowledge in low-power embedded systems, real-time operating systems (RTOS), and microcontroller-based firmware development.
  • Strong project management and communication skills.
  • Ability to work at our Irvine, CA site.

Nice to Have

  • Experience with mergers & acquisitions (M&A) due diligence in the medical device sector.
  • Experience in risk assessment, cybersecurity, and regulatory compliance for implantable devices.
  • Knowledge of ISO 13485 and FDA QSR.
  • Experience using oscilloscopes, logic analyzers, and other related tools.
  • Detailed knowledge of BLE stacks and BLE API on mobile platforms.
  • Experience in integrating BLE embedded systems with iOS, Android and Windows applications.
  • Knowledge of PC application development in Microsoft Visual Studio (e.g., C#.Net).
  • Hands-on experience with secure bootloaders, cryptographic protocols, and over-the-air firmware updates for implantable devices.

Qualifications

  • Educational background in Computer Science, Electrical Engineering, or related fields.
  • Experience in software development for medical devices and embedded systems.

Benefits & Perks

  • Anticipated compensation ranges from $99,100 to $188,300, commensurate with experience and education.
  • Core and optional employee benefits (details at www.bscbenefitsconnect.com).
  • Potential variable compensation including annual bonus and long-term incentives.
  • Support for career advancement and professional development.

Working at Boston Scientific

Boston Scientific is committed to solving important health challenges through innovation, diversity, and collaboration. The company fosters a culture of continuous improvement, knowledge sharing, and inclusion, emphasizing the importance of a diverse and inclusive workplace to drive innovation and better serve patients and communities.

Apply Now

Job Details

Posted AtJun 10, 2025
Salary99k-188k
Job TypeFull Time
Work ModeOnsite
ExperienceSenior

About Boston Scientific

Website

bostonscientific.com

Company Size

10000+ employees

Location

Irvine, CA

Industry

Medical, Dental, and Hospital Equipment and Supplies Merchant Wholesalers

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