Software Engineer – Team Leader

Purpose:

Lead the SaMD (Software as Medical Device) Team

Work Location: Rome – Italy – Viale Ostiense 131/L

Key Responsibilities: 

• Lead the SW team:
  1. Create an inspiring team environment with an open communication culture
  2. Set clear team goals
  3. Motivate team members
  4. Oversee day-to-day operation
  5. Discover training needs and provide coaching
  6. Encourage creativity and risk-taking
• Design, develop and maintain SW as Medical Devices.
• Proactively collaborate with other teams (Electronics, AI, Mechanical, Quality)
• Create and iterate user needs, risk management, and product requirements while identifying plans for verification and validation
• Identify and mitigate project risks
• Interface with internal and external suppliers, manufacturers, and customers
• Work collaboratively with project teams and engineering skillsets through all stages of development

Qualification – Required Knowledge, Skills and Abilities

• Extensive experience in C++ and Python.
• In-depth knowledge of Linux/Yocto for operating system design.
• Experience with orchestration tools and technologies for designing and managing container-based applications.
• Excellent knowledge of Git and source code management tools.
• Ability to manage and coordinate software development teams.
• Skills in defining testing strategies, implementing test automation, and ensuring software quality.
• Nice to have:
  • Knowledge of Secure Boot and security techniques for embedded systems.
  • Understanding of cybersecurity, including best practices for data protection and security of embedded applications and devices.
  • Experience in full-stack web application development (both front-end and back-end).

Minimum Required Education and Experience

• Master Degree in Physics, Mathematics, Computer Science, or Software Engineering (PhD is a plus).
• At least 5 years of experience with C and C++ (mainly standard library), and a basic knowledge of Python and Bash. Experience with GPU programming (CUDA) is a plus
• Knowledge of ISO, regulatory and legislative standards applicable to the development of medical devices
• Fluent English, written and spoken.
• Knowledge of ISO, regulatory and legislative standards applicable to the development of medical devices is a plus

Physical Requirements

• Expected travel is 30%

We support equal opportunities, without any discrimination.

The research complies with Legislative Decree 198/2006