R&D Systems Engineer II; Software/ingénieur II en systèmes de R et D
Job in
Montreal, Montréal, Province de Québec, Canada
Listing for:
Boston Scientific
Full Time
position
Listed on 2026-02-16
Job specializations:
-
Software Development
Software Engineer, Embedded Software Engineer
Job Description & How to Apply Below
Position: R&D Systems Engineer II (Software) / ingénieur II en systèmes de R et D
Location: MontrealAdditional Location(s): Canada-QC-Montreal
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance
At 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
As an R&D Systems II, Software, you will be an integral part of our product development process, ensuring that our systems meet the highest standards of performance, reliability, and compliance. You’ll work closely with cross-functional teams to translate user needs into detailed system and software requirements, develop design architectures, and contribute to risk management and validation activities. Your expertise will help us create innovative solutions in a highly regulated environment, directly impacting the success of our products and ultimately improving lives.
Your responsibilities will include:
Participate in project teams to translate user needs into software design requirements.Manage software requirements, ensuring traceability using requirements management tools.Contribute to software architecture design and integration strategies across sub-systems (software, firmware, and hardware interfaces).Document and architect communication protocols between software components and other sub-systems.Support risk management activities, including Hazard Analysis and Design FMEA for software components.Perform software-focused engineering studies and write technical reports.Provide expertise and conduct evaluation of software verification and validation activities.Initiate and document design change assessments for new and sustaining software products.Manage & maintain the JIRA backlog, prioritize software features, participate in bug triage and support agile development practices.Assist in bridging software sub-system designs and integrating features at a system level.Collaborate with cross-functional teams as an R&D representative on software deliverables.Continuously improve software development processes using agile/lean principles.Maintain strong understanding of medical device software design control processes.Required Qualifications
Bachelor's degree in software engineering, computer engineering, or a related field.2+ years of experience in product development within a regulated sector.Experience in software systems engineering and verification activities.Strong experience authoring and analyzing software requirements.Familiarity with troubleshooting software test failures.Excellent problem-solving skills in a team environment.Strong organizational, communication, and collaboration skills.Preferred Qualifications
Experience leading software development teams in a regulated environment.Understanding of embedded (real-time) software design trade-offs, performance, and redundancy issues.Extensive knowledge of advanced software testing concepts and formal verification strategies for regulated software.Strong knowledge of ISO 13485, FDA 21 CFR Part 820, and ISO 14971.Ability to interact with and influence key stakeholders internally and externally.À propos du poste
L’ingénieur(e) en systèmes R&D II travaille en collaboration avec l’équipe R&D afin de traduire les besoins des utilisateurs en exigences de conception détaillées et de gérer les spécifications des systèmes tout au long du cycle de développement du produit. Cette personne contribue à l’amélioration des processus, réalise des évaluations de risques et soutient les demandes réglementaires en s’assurant du respect des normes de l’industrie.
Le rôle exige une collaboration étroite avec des équipes multidisciplinaires pour évaluer et valider les systèmes grâce à une solide expertise en matériel, en logiciel et en ingénierie des systèmes.
Vos responsabilités comprendront :
Participer aux activités des équipes de projet afin de traduire les besoins des utilisateurs en critères de conception (p. ex. matériel,…
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