Senior Software Architect Medical Device R&D
Department : Research & Development Software Engineering
We are seeking a Senior Software Architect with direct, hands-on experience developing software for regulated medical devices . This role is part of the R&D engineering team and focuses on bringing innovative medical technologies from concept through design and verification - all in alignment with FDA QSR, EU MDR , and international safety standards .
Applications without direct experience in regulated medical device software will not be considered.
Responsibilities
- Define, document, and maintain software architecture and system-level design in compliance with FDA QSR , EU MDR , and IEC 62304 .
 - Collaborate with cross-functional R&D teams - including hardware, systems, quality, and regulatory - to ensure safe, effective, and compliant software solutions.
 - Lead architectural decision-making, ensuring traceability between requirements, design, implementation, and verification .
 - Establish and maintain software design controls , including risk management per ISO 14971 and usability engineering under IEC 62366 .
 - Provide technical leadership in software lifecycle planning, configuration management, and interface definition.
 - Review and approve design documentation, risk analyses, and verification plans to ensure architectural consistency and compliance.
 - Mentor software engineers and contribute to continuous improvement of R&D processes and toolchains.
 - Support cybersecurity, data privacy , and interoperability considerations in line with AAMI TIR57 and IEC 81001-5-1.
 
Qualifications
Bachelors or Masters degree in Software Engineering, Computer Science, Electrical Engineering, or a related technical discipline.8+ years of software development experience, with at least 4 years in medical device software architecture or design .Deep understanding of IEC 62304 , ISO 13485 , ISO 14971 , and FDA design controls .Proven track record architecting embedded , connected , or cloud-integrated medical systems .Strong background in C++, C#, or Python ; experience with software frameworks and toolchains for regulated environments.Excellent analytical, documentation, and communication skills - able to bridge software, hardware, and regulatory perspectives.#SaMD #MedTech #DigitalHealth #MedicalDevices #SystemsEngineering #IEC62304
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