Job Description
SYSTEMS ENGINEER – INTEGRATION
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Location: Pleasanton, CA
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Duration: 1 year, possible extensions
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Overview
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Seeking a senior-level Systems Engineer to lead system-level integration for complex, regulated medical devices. The engineer will coordinate the integration of hardware, embedded software, mechanical components, mobile applications, wireless technologies, and cloud-connected services across new product development and sustaining programs.
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Responsibilities
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- Lead system integration planning and execution across the full product lifecycle.
- Define the integration strategy, sequencing, interface definitions, and mitigation of integration risks.
- Support system architecture, integration requirements, and interface control across hardware and software domains.
- Coordinate end-to-end integration across embedded firmware, mechanical, mobile, wireless, and cloud components.
- Ensure requirements are clear, allocatable, and integrable across engineering disciplines.
- Identify integration issues early and drive them through root-cause analysis and resolution.
- Ensure integrated systems are traceable, test-ready, and prepared for formal verification and validation.
- Communicate technical risks, tradeoffs, system impacts, and project status to cross-functional teams and leadership.
- Support design transfer, sustaining activities, and applicable quality-system requirements.
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Target Background
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- Bachelor’s degree with approximately 5–6 years of relevant experience, or a master’s degree with at least 4 years of relevant experience.
- Demonstrated experience leading system integration for complex products involving both hardware and software.
- Strong understanding of system architecture, interface control, integration sequencing, and multi-component system behavior.
- Hands-on experience working across Systems, Software, Hardware, and Test Engineering.
- Experience in regulated product development; medical device experience is strongly preferred, although aerospace, automotive, or similar industries may be considered.
- Working knowledge of design controls, configuration management, defect tracking, and change-management processes.
- Experience supporting Class II/III medical device submissions is highly desirable.
- Experience with DOORS, JIRA, or similar requirements and defect-management tools.
- Familiarity with IEC 62304, IEC 60601, ISO 14971, or comparable standards is preferred.
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Experience integrating mobile applications, Bluetooth, Wi-Fi, cloud services, embedded firmware, and automated electromechanical system tests is preferred
