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Firmware Software Engineer
2 months ago
At Boston Scientific, we're committed to advancing science for life by developing innovative medical solutions that improve patient lives. We're seeking a highly motivated and experienced Senior Firmware Engineer to join our Hardware R&D team.
About the Role:
As a Senior Firmware Engineer, you'll have the opportunity to own and drive portions of the design while being part of an experienced design team. You'll be responsible for developing and testing software as part of a system, documenting and troubleshooting issues, and working with instrument and hardware.
Key Responsibilities:
- Develop and test software as part of a system, document and troubleshoot issues, and work with instrument and hardware.
- Participate in software system architecture development and document software requirements and development plan.
- Perform detailed design analysis and reviews with hardware engineering team to achieve product performance, cost, reliability, and manufacturability requirements.
- Track software-related issues and lead resolution of issues with a well-documented and methodical approach.
- Develop software test and verification plans and protocols, and conduct prototype testing and verification testing.
- Work closely with hardware and software engineering teams to debug/integrate software with the product.
- Collaborate with program managers to create and manage development plans and project plans related to software development.
- Contribute to the creation and update of relevant software documentation, risk management documentation, issue tracking, configuration management, test reports, etc.
Requirements:
- 5 years' experience in embedded software design.
- Experience developing firmware solutions using C, C++, and Assembly for microcontrollers/microprocessors (experience with or without RTOS, event-driven, and state machines designs preferred).
- Experience in technical specification and report writing.
- Experience with unit test and system test of embedded software systems.
- Must be able to read, write, and speak fluent English, and must possess excellent communication skills, both written and oral. Working French is also necessary.
Preferred Qualifications:
- Experience with Medical device development or other highly regulated industries is an asset.
- Familiarity with medical device design control regulations (IEC 60601, IEC 62304, ISO) is an asset.
- Ability to organize and move project tasks forward in an orderly and structured fashion.
- Effectively communicate issues/problems and results that impact timelines, accuracy, and reliability of project status.
Join our team of innovators and make a meaningful difference in people's lives.