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Principal Software Architect

4 months ago

Fort Lauderdale, Florida, United States OBVIUS Robotics, Inc. Full time

An exciting opportunity to be in the early start up stage at OBVIUS Robotics, a well-capitalized medical device company advancing technology in Central Venous Access.

This role will oversee the development and continuous improvement of cutting-edge software systems that drive functionality, performance and safety of innovative medical devices.


Essential Job Functions:

  • Define and design high-level software architecture, ensuring scalability, modularity, and reliability.
  • Develop the overall software roadmap and strategies to meet the stringent requirements of medical device standards.
  • In-depth knowledge of real time operating systems (RTOS) principles and operation.
  • Strong understanding of software-hardware interactions and the ability to optimize and test software for embedded platforms.
  • Knowledge of wireless communication standards including Bluetooth and Wi-Fi.
  • Lead efforts to ensure software development complies with IEC 62304, including documentation, risk management, and traceability.
  • Establish and maintain software lifecycle processes in alignment with regulatory standards.
  • Implement robust cybersecurity measures to protect sensitive patient data and device integrity.
  • Stay current with evolving cybersecurity threats and best practices and integrate them into the development process.
  • Familiarity with IEC and related medical device software development standards.
  • Provide technical leadership and mentorship to the software development team.
  • Foster a culture of excellence, compliance, and continuous improvement.
  • Oversee seamless integration of software components with the various systems, ensuring interoperability and safety.
  • Collaborate closely with hardware engineers to optimize system performance.
  • Drive the development of advanced algorithms for robotics control, sensor fusion, and data analysis.
  • Optimize algorithms for real-time performance, safety, and regulatory compliance.
  • Enforce software development best practices, including code reviews, testing, and documentation.
  • Establish rigorous testing protocols to verify software functionality, safety, and compliance.
  • Serve as a key point of contact for regulatory agencies regarding software-related inquiries.
  • Support audits, inspections, and related activities for software development compliance including 3rd party testing with NRTLs such as TUV, ETL, and UL.
  • Perform other related duties incidental to the work described herein.

Qualifications:

  • Bachelor's, Master's, or PhD degree in Electrical Engineering, Computer Science, Software Engineering, or related field.
  • 15+ years of experience in software architecture and development for complex systems, preferably in medical device or healthcare industries.
  • Proficiency in programming languages such as C, C++, Python, or Java.
  • In-depth knowledge of IEC 62304 and experience in its practical application.
  • Strong background in FDA software development best practices.
  • Familiarity with medical device regulatory standards, including FDA regulations and ISO 13485.
  • Exceptional problem-solving skills in complex, safety-critical environments.
  • Excellent leadership, communication, and collaboration skills.
  • Ability to travel as needed to support development, product testing, and customer support.

Location:
South Florida, East coast