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Insulet Corporation Logo

Senior Software Requirements & Systems Engineer (Medical Devices) (Hybrid)

Insulet Corporation

$109,800 - $164,700
Sep 3, 2025
CA, US
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Insulet is looking for a Software Requirements Engineer to lead the creation, analysis, and governance of software requirements for their next-generation wearable medical device, spanning mobile and cloud. This role is crucial for ensuring the quality and traceability of requirements in a regulated environment, supporting the development of innovative medical technology.

Requirements

  • Proven expertise writing and managing software and/or system requirements with strong decomposition, clarity, and testability.
  • Demonstrated knowledge of systems engineering practices: requirements management, risk analysis, and software/system architecture concepts.
  • Working knowledge of ALM tools (e.g., Polarion, Helix ALM, DOORS) and traceability methods.
  • Medical device standards: IEC 62304, ISO 14971, ISO 13485, 21 CFR 820.30.
  • Formal training/certifications in Systems Engineering or Requirements Engineering (e.g., INCOSE, IREB/CPRE).
  • Familiarity with diabetes management products, mobile/cloud, IoT, cybersecurity/privacy (e.g., GDPR).
  • Background with analogous safety standards (DO-178C, ISO 26262, IEC 61508) with willingness to map to IEC 62304.

Responsibilities

  • Elicit, write, and refine clear, testable software requirements from user needs and product requirements.
  • Build and maintain bidirectional traceability across user needs, hazards/risks, software requirements, design/architecture, and verification - per IEC 62304 and ISO 14971.
  • Generate trace reports for regulatory submissions and audits.
  • Administer and improve requirements in ALM/PLM (e.g., Polarion/Helix/DOORS + PLM), including versioning/baselining.
  • Review downstream artifacts (architecture/design, DFMEA/FMEA, test strategy/cases) to ensure implementation meets requirements.
  • Partner with Product Owners to translate requirements into Agile user stories with adequate acceptance criteria.
  • Contribute to continuous improvement of requirements practices, templates, and tool workflows.

Other

  • 5+ years contributing to complex, safety-critical or regulated products (medical device preferred; aerospace/avionics, automotive, rail, or industrial safety acceptable).
  • Experience operating under a QMS/design controls and collaborating across Software, Systems, V&V, Quality, and Product.
  • Comfortable in Agile environments; able to align Definition of Ready/Done with regulatory needs.
  • Exceptional facilitation, documentation, and stakeholder communication skills.
  • This position is eligible for hybrid working arrangements (requires on-site work from an Insulet office at least 1x/week; may work remotely other days).