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Tier-1 employer, metro Bengaluru location, and broad senior engineering leadership role increase applicant competition.
Requires regulated medical device delivery and specific platform integration skills, limiting cross‑industry transferability.
Explicit 12–15+ years, regulated software and specific tech (.NET, C#, FDA/ISO) create strict mandatory filters.
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Lead the Service R&D Software Engineering team for remote troubleshooting and diagnostics within a regulated product environment.
Own end-to-end delivery of system and software releases, ensuring on-time execution, quality, and compliance with regulatory standards.
Oversee workforce planning, technical direction for system architecture, cross-functional stakeholder alignment, and continuous process improvement in Agile/Lean, FDA, ISO, and cybersecurity frameworks.
12–15+ years of professional software development experience with a bachelor's or master's degree in computer science, engineering, or related field.
Expertise in C#.NET, Windows Services, REACT JS, HTML, JavaScript on .NET core/framework, and REST APIs; exposure to cloud technologies (e.g., AWS) and embedded systems preferred.
4+ years of direct personnel management experience and 3+ years leading complex multi-team software projects with accountability for delivery milestones and quality.
Proven experience delivering software products in regulated environments (e.g., FDA, ISO 13485 compliance). Onsite role based in Bengaluru.
Experienced leader in regulated software product development, ideally with multi-disciplinary global team management and structured improvement methodology experience (e.g., Danaher Business System).
Skilled in managing cross-functional stakeholder engagement and translating customer insights into product enhancements across platforms.
Familiarity with life sciences, biotechnology, or medical instruments industry and working within Quality Management Systems and GMP environments is a plus.