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Strong Tier-1 brand and metro location increase competition despite niche regulated-medical-device seniority.
Strong bias toward medical-device regulatory and principal architecture experience, limiting cross-industry transferability.
Requires 18+ years, regulated-medical-device experience, principal architect track record, and specific technical plus compliance expertise.
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Lead architecture and design of desktop, web, and mobile platform software solutions, ensuring scalability, security, and regulatory compliance.
Drive alignment of software architecture with product strategy, regulatory standards (FDA, ISO), and long-term technology vision across Acute Care & Monitoring R&D.
Provide technical leadership and mentorship to senior engineers, reduce technical complexity and debt, and integrate quality and compliance within Agile development cycles.
Minimum 18 years of software engineering experience.
Bachelor’s degree in Computer Science, Engineering, or related field (Master’s or PhD preferred).
Proven lead architect/principal designer on at least two end-to-end software development projects for Windows desktop or mobile applications.
Experience developing medical device software in regulated environments; expertise with FDA and ISO standards.
Senior-level technical leader with deep experience in enterprise architecture for desktop, web, and mobile applications, especially in medical device regulated environments.
Strong expertise in C++, C#, UI frameworks (React, Angular, WPF, Qt), design patterns, and CI/CD/DevOps practices.
Experience working with global distributed teams and driving architectural decisions that reduce complexity and improve scalability and compliance.