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Senior role with niche medical-device WPF expertise but multinational brand and remote option increases applicant pool.
Medical device regulatory experience and specialized Windows/WPF embedded knowledge limit cross-industry transferability.
Explicit 8-12 years and specific mandatory C#/.NET WPF and medical device experience make filters strict.
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Lead design and development of medical device software, specifically console software for diagnostic instruments under clinical chemistry and immunoassay domain.
Own architecture, coding, unit testing, and adherence to quality, performance, scalability, reliability, and regulatory compliance including FDA and ISO standards.
Collaborate cross-functionally with software V&V teams and distributed teams to deliver products meeting schedule and quality goals.
Bachelor’s degree in Computer Science, Software Engineering, Computer Engineering, or related field.
8-12 years experience in development of commercial products, preferably electro-mechanical instruments.
Strong experience in C# .NET and WPF, including real-time transaction processing and SQL database persistence.
Work location: Bangalore (on-site role). Knowledge of FDA Quality Systems Regulation is desirable.
Experienced in software development for medical devices or healthcare industry with exposure to regulatory standards (FDA, ISO).
Skilled in complex data presentation layer development and low-level Windows programming.
Able to operate in cross-functional, distributed team environments and contribute to both design and quality assurance processes.