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Tier-1 employer, metro location, and broad senior technical skillset increases candidate competition.
Extensive medical-device regulatory and enterprise-architecture needs drive high industry specificity.
Mandatory 18 years, principal architect experience and regulated-medical-device expertise create strict shortlisting filters.
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Lead architecture and design of secure, scalable software solutions across desktop, web, and mobile platforms, ensuring innovation and regulatory compliance (FDA, ISO).
Collaborate with engineering leadership and cross-functional teams to drive technical strategies, design reviews, and engineering best practices within an Agile environment.
Provide technical leadership and mentorship, reducing architectural complexity and technical debt while ensuring quality, testability, and compliance by design.
Minimum 18 years of software engineering experience including leading at least two end-to-end software development projects for Windows desktop or mobile applications.
Bachelor's degree in Computer Science, Engineering, or related field; Master's or PhD preferred.
Extensive experience in developing regulated medical device software and compliance with FDA, IEC 62304, and ISO standards.
Expertise in Python, C++, C# and proficiency in UI/UX frameworks (React, Angular, WPF, Qt), enterprise architecture, microservices, API development, and CI/CD pipelines.
Experienced in technical leadership roles within regulated medical device software development environments involving global, distributed teams.
Strong background in enterprise architecture with practical experience in scalable system design, integration strategies, and regulatory compliance.
Comfortable working in Agile Scrum environments and adept at mentoring senior engineers and technical leads to foster innovation and engineering excellence.