Embedded Software Engineer

2 months ago


Montreal, Quebec, Canada Boston Scientific Gruppe Full time
Job Summary

Boston Scientific Gruppe is seeking a highly motivated and experienced Embedded Software Engineer to join our Hardware R&D team. As a Senior Firmware Engineer, you will be responsible for developing and testing software for first-of-a-kind, 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.
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.


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