Senior Lead System Integrator

Senior Lead System Integrator

LivaNova

Mirandola, Italy

We’re seeking a motivated and experienced Senior Lead System Integrator to drive technical tasks and deliverables for an innovative Sensing Technology project.

In this role, you will be accountable for the R&D function within our project core team, coordinate the planning and execution of R&D tasks, oversee technical resources, and drive Design Control processes to ensure our product meets the highest standards of quality, safety, and performance.

You’ll collaborate closely with the Project Head and the cross-functional managers, taking ownership of technical excellence as well as of costs and timelines. Working across organizational boundaries, you will ensure smooth execution, proactively anticipate challenges, and keep projects moving forward effectively.

Duties and Responsibilities

• Collaborate with project head and functional teams to ensure R&D project deliverables meet quality, cost, and schedule goals;
• Contributes to create, maintain and execute project plans for the specific technical contents, and to proactively identify project risks and mitigations, in collaboration with the project head;
• Coordinate with PMO and other inter-related functions to establish project operating mechanisms, and to ensure effective resources allocation;
• Facilitate clear communication and coordination among R&D teams, ensuring seamless information flow from project leadership down to engineering teams.

The Individual

• Degree in Electronics Engineering, Chemical, Biomedical Engineering, or an equivalent scientific field;
• Experienced in leading complex R&D projects, ideally with a background in sensing technologies or related fields;
• A collaborative leader with excellent communication skills, able to work effectively across multidisciplinary and multicultural teams;
• Strong knowledge of design and development processes, including Design Control and risk management;
• Familiar with quality and regulatory standards such as FDA Quality System Regulations, ISO 13485, and Medical Device Directive;
• Comfortable applying statistical methods, with familiarity in Design for Manufacturability and Six Sigma principles considered a plus;
• Basic understanding of process validation techniques;
• Proficient in English and Microsoft Office tools;
• Adaptable and proactive, with a proven ability to manage competing priorities and navigate complex organizational structures.

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