Sr. Systems Engineer, Caregiver Solution (Hybrid)
Insulet CorporationAbout the role
Job Profile Name Senior Systems Engineer
Job Code EN.SYENG.SYE.P3.US1
Include Job Code in Name No
Job Profile Summary
Position Overview:
The Senior Systems Engineer is a member of the Systems COE and a technical expert responsible for supporting systems engineering activities for various applications newly developed and/or enhanced by the Mobile & Cloud Software Engineering group. The position will directly involve hands on development of system and software requirements, system architecture, non-functional requirements, grey box testing, integration testing for android and iOS mobile applications that support the Insulet Product Eco-System. Education and work experience should encompass an engineering discipline in computer science, systems engineering or related field and should have prior work experience in cloud-based products, mobile applications, understanding of data models, enterprise system performance and scalability. This position will report to Sr. Manager, Systems Engineering.
Responsibilities:
• Serve as a key member of a cross-functional project team consisting of software, analytics, Site reliability engineers, Cloud Operations, Medical, Marketing, Data engineering, Privacy, Regulatory, Product owners, Product Managers and quality engineers to achieve project deliverables
• Lead system definition tasks such as generating user needs, product/system requirements, software requirements and use-case descriptions
• Contribute to system development by defining system and subsystem architecture
• Identify and document System Hazard Analysis, failure modes and risk mitigation
• Provide system impact and safety risk assessment of component failure modes as input to DFMEA
• Triage and/or troubleshoot production issues and incorporate into requirements and risk documents
• Develop performance models and non-functional requirements in support of system scalability and performance
• Serve as technical consulting resource for integration, subsystem and system verification activities creating integration plans, perform review of test coverage and hands on integration testing
• Create and maintain traceability among design input, design output, verification and validation, and risk management artifacts to ensure completeness and fully traceable design history file
• Participate in review of data models and generate data mapping, data driven requirements as needed. Work with data engineering and architecture team to generate data specification
Education and Experience:
• Bachelor of Science or equivalent degree in Software Engineering, Computer Science or related field is required
• 5-7 years of overall experience in software industry in engineering or related roles
• 5+ years of experience working as a Systems engineer in enterprise applications, or related
• 3+ years hands on experience in developing non-functional requirements and supporting system integrations including grey box testing, or related
Minimum Requirements:
• Demonstrated expertise in Systems Engineering practices such as requirements management, design trade-off and cost-benefit analysis, hazards and risk assessments
• Experience writing verification plans, protocols and reports in a regulated industry
• Proficient with Medical Device regulations (IEC 62304, 21 CFR part 820.30-Design Controls)
• Excellent project team skills working collaboratively under a Quality Management System (QMS), as part of a cross-functional team that includes development, verification/validation, marketing, clinical, regulatory and quality experts
• Good understanding of web services, microservices, HTTP protocols, REST APIs, SOA
• Familiarity with database concepts and usage
• Exposure to data models, data driven requirements
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