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Tier-1 brand and Hyderabad metro presence with senior, regulated-medical-device specialization yields medium competition.
Regulatory and medical-device architecture requirements strongly limit transferability, so background fit sensitivity is high.
Explicit 18-year minimum and mandatory regulated medical-device architecture experience make shortlisting highly strict.
Lead architectural decisions and design for secure, scalable desktop, web, and mobile software solutions in regulated medical device environments.
Provide technical leadership, mentor senior engineers, and drive innovation while reducing architectural complexity and technical debt.
Ensure compliance with FDA, ISO, and quality processes throughout the software development lifecycle within an Agile environment.
Minimum 18 years of software engineering experience with expertise in architecture and design for desktop, web, and mobile platforms.
Bachelor’s degree in Computer Science, Engineering, or related field; Master’s or PhD preferred.
Proven experience as lead architect/principal designer for at least two end-to-end software projects in Windows desktop or mobile applications.
Extensive experience in medical device development and regulated environments; proficiency in Python, C++, C#; knowledge of UI/UX frameworks like React, Angular, WPF, Qt, and CI/CD practices.
Senior-level professional with deep expertise in enterprise architecture, microservices, advanced API development, and scalable system design for complex applications.
Experienced in leading global distributed teams with strong communication and mentorship skills focused on innovation and engineering excellence.
Familiar with regulatory compliance in healthcare software (FDA, IEC 62304), agile methodologies, and integration of emerging technologies in medical device software.