Insulet

Medical Device

Sr.SystemsEngineer,DataProducts

$113–169k United States FULL TIME Remote Friendly
The Brief

“Sr. Systems Engineer, Data Products at Insulet. Skills: Systems Engineering, Requirements Management, System Architecture, Mobile Applications. Lead system definition tasks. Contribute to system development”

What You'll Achieve.

deliver safe, reliable, and high-impact solutions for patients; strengthening product quality

Industry & Context.

Medical Device
Problems you'll solve

troubleshoot production issues; risk mitigation

What They're Looking For.

Must Have

Systems Engineering practices, requirements management, design trade-off and cost-benefit analysis, hazards and risk assessments, writing verification plans, protocols and reports in a regulated industry, Medical Device regulations (IEC 62304, 21 CFR part 820. 30-Design Controls), project team experience, working collaboratively under a Quality Management System (QMS), web services, microservices, HTTP protocols, REST APIs, SOA, database concepts, data models, data driven requirements, data governance, 5-7 years of overall experience in software industry, 5+ years of experience working as a Systems engineer in enterprise applications, 3+ years hands on experience in developing non-functional requirements, supporting system integrations, grey box testing

Nice to Have

Master of Science degree, System Engineering training, System Engineering certification, integrating/testing cloud connected mobile applications on Android/iOS platforms

What You'll Do.

Lead system definition tasks

Contribute to system development

Identify and document System Hazard Analysis

Provide system impact and safety risk assessment

Triage and/or troubleshoot production issues

Develop performance models and non-functional requirements

Serve as technical consulting resource

Create and maintain traceability

Participate in review of data models

How You'll Work.

Team & Collaboration

Serve as a key member of a cross-functional project team; working collaboratively under a Quality Management System (QMS); part of a cross-functional team that includes development, verification/validation, marketing, clinical, regulatory and quality experts

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