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Strong employer brand plus metro location and broad senior role skills create moderate candidate competition.
Requires regulated medical-device and enterprise architecture experience, reducing cross-industry transferability significantly.
Explicit 18+ years, regulated medical-device experience, and specific tech and architecture mandates enforce high strictness.
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Lead architecture and design of secure, scalable desktop, web, and mobile software solutions, including new system development from scratch.
Drive technical leadership by mentoring senior engineers, reducing architectural complexity and technical debt, and ensuring quality, testability, and regulatory compliance in a fast-paced Agile environment.
Collaborate with cross-functional global teams to align on technical strategies, regulatory requirements (FDA, ISO), and deliver high-performance enterprise software solutions.
Minimum 18 years of software engineering experience, with proven lead architect/principal designer roles for at least two end-to-end software projects.
Bachelor’s degree in Computer Science, Engineering, or related field; Master’s or PhD preferred.
Experience in medical device software development within regulated environments (FDA, IEC 62304 compliance).
Proficiency in Python, C++, C# and modern UI/UX frameworks (React, Angular, WPF, Qt); experience with design/modeling tools and CI/CD pipelines.
Strong background in enterprise architecture with deep expertise in microservices, API development, and scalable system integration in complex, regulated environments.
Experience leading and mentoring senior-level engineering teams in Agile/Scrum setups across global, distributed teams.
Demonstrated ability designing and delivering medical device software complying with FDA and ISO standards, and familiarity with emerging technology integration and regulatory landscapes.