Job Description Summary

Job Description

Responsibilities

• Write clean, well-documented, and maintainable code in C/C++ and other relevant languages.
• Participate in reviews , investigations and other relevant activities.
•  Develop the device in compliance with medical device standards (e.g., ISO 13485, IEC 62304).
•  Ensure adherence to safety critical software development practices, including risk management and failure mode analysis.
•  Develop and execute test plans for unit, integration, and system level testing.
• Use debugging tools and techniques to troubleshoot and resolve firmware issues.
• Create and maintain comprehensive documentation, including specifications, design documents, and tests
•  Contribute to the preparation of documentation required for regulatory submissions.
• Document and track software defects and issues throughout the development lifecycle.
  
   

Skills and experience

• 4-9 years of experience in embedded software development/test
• Good experience in C/C++ with at least 2 years in medical device industry.
• Strong understanding of embedded systems and hardware-software integration.
•  Familiarity with testing methodologies and tools used in embedded software development.
• Experience with software development lifecycle (SDLC) tools and methodologies.
• Familiarity with version control systems (e.g., Git) and software development lifecycle (SDLC) tools.
• Excellent problem solving, analytical, and debugging skills.
• Strong communication skills and ability to work effectively in a team-oriented environment.

Good to have

• Strong knowledge of medical device standards (e.g., IEC 62304, ISO 13485).
• Familiar with FDA guidelines and 510K submission process
• Experience in trackwise tool and familiarity with CAPA process are added adavatages
•  Knowledge of cybersecurity principles in embedded systems is an advantage.

Required Skills

Optional Skills

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Primary Work Location

Additional Locations

Work Shift