Embedded Software Architect

3 days ago

Melbourne, Victoria, Australia beBeeMiddleware Full time $125,000 - $160,000
Middleware Software Engineer Opportunity

This role offers a chance to connect embedded firmware systems with higher-level software applications and clinical platforms.

The ideal candidate will bring a strong background in C#, Visual Studio, .NET, API development, and real-time device communication, preferably within a regulated medical environment.

Key Responsibilities:
  • Design and Development: Create ASP.NET Web API applications for ingesting, processing, and exposing data from medical hardware systems.
  • Integration and Data Collection: Integrate with hardware device APIs to collect, measure, and analyze ionizing radiation data for quality assurance.
  • Real-Time Data Streaming: Implement real-time data streaming using SignalR, allowing clinicians and systems to interact with live device data.
  • Maintenance and Improvement: Maintain and improve Windows Communication Foundation (WCF) services and Windows Services for reliable transmission of data from distributed devices to on-prem servers.
  • Data Storage and Retrieval: Build and optimize data storage/retrieval workflows using Entity Framework with SQL Server and MongoDB, including writing and optimizing SQL queries.
Requirements:
  • 7+ years of experience in middleware, backend, or systems software engineering
  • Highly proficient in C#, Visual Studio, and .NET, including ASP.NET Web API and WCF
  • Strong understanding of HTTP methods, Web APIs, and REST principles
  • Experience developing and maintaining Windows Services
  • Experience integrating with hardware or embedded systems APIs
  • Proficiency with Entity Framework, SQL Server, and MongoDB, including writing and optimizing SQL queries
  • Experience with real-time communication using SignalR or similar frameworks
Preferred Skills:
  • Background in radiation oncology, medical physics, or QA of therapy devices
  • Experience developing or supporting dose calibrators, PACS/RIS, or clinical QA software
  • Understanding of FDA 21 CFR Part 820, ISO 13485, IEC 62304, or similar compliance frameworks

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