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We are seeking a highly motivated and experienced Senior Firmware Engineer to join our Electrophysiology team at Boston Scientific Gruppe. As a key member of our Hardware R&D team, you will be responsible for designing, developing, and testing embedded software for our life-changing medical devices.
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.
- Bachelor's degree in Computer Science, Electrical or Computer Engineering or related field.
- 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).
- Must be able to work with hardware lab equipment.
- 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.
- 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.
As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate.