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Strong employer brand plus metro location but senior specialist role reduces applicant density.
Highly specialized medical-device and regulated-software expertise limits cross-industry portability.
Explicit 17+ years, regulated-medical experience, and technology/regulatory mandates create strict filtering.
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Lead multiple software engineering teams (Development, Test/QA, DevOps) to deliver high-quality software products in a regulated environment focused on medical devices.
Drive technical strategy, ensure compliance with standards (FDA, ISO, IEC), and collaborate cross-functionally with architects, product, quality, regulatory, and engineering teams for product roadmap alignment.
Manage talent development, execution oversight, and foster engineering excellence through Agile, DevOps practices, automation, and data-driven decision-making to achieve predictable delivery and product quality.
17+ years of software engineering experience including leadership in desktop, connected, medical device, or healthcare software products.
Degree in Computer Science, Electronics, Electrical Engineering, Software Engineering, or related field (B.E./B.Tech./M.E./M.Tech.).
Strong knowledge of desktop application frameworks such as WPF, WinForms, WinUI, C#, .NET, C++ or similar.
Experience working in regulated industries (medical devices, healthcare, life sciences, automotive, aerospace, industrial automation) with applicable quality and compliance frameworks (FDA, ISO 13485, IEC 62304, ISO 14971).
Proven leadership managing cross-functional software engineering teams delivering complex regulated software products in Agile environments.
Strong expertise in desktop software architecture combined with experience in connected medical device software and compliance requirements.
Data-driven with demonstrated ability to drive engineering excellence via Agile, DevOps, automation, and quality metrics in a regulated, multi-stakeholder context.