R&D Manager

Mission

The Requirements & Verification group is part of the Systems Engineering department formed by brilliant and passionate engineers. You will Lead the Requirements, Risk and Verification for Imaging systems. You are in charge to lead several experts throughout the design and the development of world leading solution for image guided Proton Therapy. You will provide a frame, operational management, and interface management with the business stakeholders to ensure systems requirements, safety and verification engineering practices to allow a robust design control and a framed innovation framework for Imaging systems of the Proteus235®.

Challenges we trust you with

• Ensure operational management of your team by analyzing project needs, defining a suitable working structure, planning and efforts for your team with project / program managers. You prepare quarterly and yearly budget / planning exercises with the Head of PT R&D SYSTEMS and program management
• Organize the workload in your team - follow the projects’ progress and adapt to changes required to provide in quality & time. You also take part actively in the coordination of release activities involving your team
• Manage team’s HR matters: recruitment, career management, feedback and evaluation. You are Safety and well-being of your team members and administrative HR aspects
• Provide guidance to your team members to ensure the overall quality of the work and to monitor their individual progress and qualities by suggesting ways of improvement
• Lead the improvements of system engineering methods and tools by collecting, suggesting, and implementing changes in agreement with the experts

What we value

You have: 

• Science or Engineering degree with at least five years’ experience in a regulated environment
• Experience in application of structured development processes in complex software development; preferably supervision software for a complex system
• Experience in application of IEC / ISO standards to electrical medical devices
• Knowledge of the following disciplines are strong assets: SW development for Medical devices, Electrical safety, cybersecurity, usability engineering, risk management, X-ray / radiation safety
• A first experience as a team coordinator / supervisor or experience as project manager in a complex regulatory sensitive environment is required
• Experience in interacting with internal and external third parties, including subcontractors and regulatory authorities
• Excellent oral and written communication skills in English 

And you also are:

• Able to communicate, facilitate and focus on promoting solutions, even in exposed or stressful situations
• Able to balance appropriately strict respect for project objectives with quality of the product and teams’ well-being. You care for their specific constraints and arbitrate with empathy
• Quality focused, working for the highest value for your stakeholders
• Able to apply regulatory and quality constraints in a critical and complex environment. Medical devices framework is a plus

Life at IBA

At IBA, we value creativity, innovation, and a commitment to excellence. As a certified B Corporation (B Corp), we uphold the highest standards of social and environmental performance. If you’re ready to embark on a journey where your skills and ideas can truly make an impact, apply now to join our dedicated team. Let’s shape the future of technology together!

Apply today and be part of a mission that matters!