Senior System Verification Engineer

As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow—because at LivaNova, we don’t just treat conditions — we aspire to alter the course of lives. Who are we looking for : Are you passionate about testing complex systems and ensuring that innovative medical devices meet the highest standards of safety, performance, and regulatory compliance? We are looking for a Senior System Verification Engineer to join our R&D team and play a key role in the verification of integrated hardware and software medical devices throughout the product development lifecycle. In this role, you will lead system-level verification activities, working closely with Systems Engineering, Software, Hardware, and Quality teams to ensure product requirements are fully verified and documented according to international standards and regulatory expectations. Your new role : Lead the definition and execution of system verification strategies for complex medical devices. Translate system requirements into comprehensive verification plans, protocols, test cases, and traceability matrices. Execute and coordinate system-level testing activities, including functional, performance, usability, and safety verification. Collaborate with Systems Engineering, Software, Hardware, and Quality teams to ensure complete requirements coverage. Analyze test results using statistical methods and prepare technical reports to support product development decisions. Investigate verification failures, identify root causes, and support corrective actions. Manage verification activities, including planning, scheduling, resource allocation, and progress tracking. Ensure verification documentation is audit-ready and compliant with applicable regulatory requirements. Support risk management activities and contribute to product safety assessments. Contribute to regulatory submissions and support internal and external audits. Mentor junior engineers and promote best practices in system verification and validation. Drive continuous improvement initiatives related to verification processes, methodologies, and tools. How you'll make an impact : Ensure that medical devices are thoroughly verified and meet customer, quality, and regulatory requirements. Contribute to the development of safe, reliable, and high-performing healthcare technologies. Support successful product launches through robust verification planning and execution. Strengthen collaboration between engineering disciplines and quality functions. Improve product quality by…