Lead SWE, Full Stack
Hybrid · Newark, Delaware, United States
Job Summary
Lead technical design, development, and documentation of software components and systems for safety-critical, regulated medical devices; hands-on with C#, WPF, and .NET; mentor junior engineers; collaborate across product, engineering, and clinical teams to maximize value; own system-level documentation and ensure compliance with safety, functional, and regulatory requirements; drive continuous improvement in team processes, architecture, and software quality; communicate progress, risks, and needs to management and cross-functional teams. Responsibilities include leading design, developing and testing software, guiding Agile practices, and ensuring quality and regulatory compliance, while working with stakeholders to deliver impactful software for clinical/internal use.
Required Qualifications
- BS or MS in a related technical field
- 8+ years of software development experience (6+ with Master’s, 3+ with PhD)
- Expertise in object-oriented and procedural programming (C#, C++, Java, .NET)
- Experience with safety-critical software in regulated environments (FDA, etc.) preferred
- Familiarity with version control tools (Git, Azure Dev Ops, etc.), SDLC, and large codebases
- Experience with cybersecurity, cloud computing, or deep learning is a plus
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