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Software Architect

Suntra MedTech Solutions
Posted 4 months ago, valid for 10 days
Location

Bedford, NH 03110, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • The position is for a high-level architect and designer of medical device software based in Bedford, NH, requiring 10+ years of industry experience.
  • The role involves collaboration with project managers and software teams, focusing on code quality, regulatory compliance, and risk management.
  • Key responsibilities include developing secure software architecture, conducting code reviews, and ensuring adherence to standards like IEC 62304.
  • Candidates should possess a Bachelor's degree in a relevant field and be proficient in programming languages such as C, C#, C++, and JavaScript.
  • The position offers a competitive salary, commensurate with experience, and the opportunity to lead technical initiatives in medical device development.

Description

Position Overview: Responsible for the high-level architecture and design of medical device software, ensuring alignment with system and software requirements. This “hands-on” role requires you to be in our Bedford, NH office (on a scheduled basis) to collaborate with project managers and software teams on multiple projects. The role includes reviewing detailed designs, the testing structure, and code, while also focusing on risk management and cybersecurity to ensure device safety for users and clinicians. It also offers the chance to lead technical initiatives, guide engineering teams, and make a significant impact on the development of medical devices.


Key Responsibilities:

  • Architecture & Design: Develop scalable, secure, and compliant software architecture based on system and software requirements.
  • Collaboration & Leadership: Work closely with project managers and software teams, providing architectural guidance and mentoring engineers.
  • Code Quality & Reviews: Conduct code reviews, enforce coding standards, and ensure high-quality, maintainable code.
  • Regulatory Compliance: Ensure adherence to regulatory standards (e.g., IEC 62304) for medical device software.
  • Risk Management & Cybersecurity: Integrate safety measures and conduct risk assessments to ensure device safety.
  • Continuous Improvement: Advocate for best practices, evaluate new technologies, and enhance development processes.

Requirements

Qualifications:

  • Required: Bachelor’s degree in software engineering, Computer Science, Electrical Engineering, or a related field; 10+ years of industry experience; proficiency in programming languages (e.g., C, C#, C++, JavaScript); experience with embedded systems, and medical device development; familiarity with Agile/Scrum processes.
  • Beneficial: Master’s degree; experience in Class B and C medical devices; Linux OS configuration; familiarity with test-driven development (TDD), CI/CD, and regulatory standards like IEC 62304.
  • Preferred: Experience using generative AI to aid in software development, developing machine learning-based products, knowledge of embedded Linux, real-time operating systems (RTOS), and cybersecurity hardening, as well as familiarity with Atlassian tools and software development best practices.



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