Senior Quality Systems Lead – Medical Devices

Jefferson Wells Italia cerca una figura Senior Quality Systems Specialist per conto di una multinazionale biomedicale specializzata in dispositivi per dialisi e terapie renali con stabilimento a Mirandola. La risorsa sarà responsabile della supervisione di programmi e sistemi di qualità, supporto alle normative, e collaborazione con le funzioni...

LivaNova PLC in Mirandola, Italy, is seeking a Senior System Verification Engineer to lead verification strategies across complex medical devices throughout the product lifecycle.You will translate requirements into comprehensive verification plans and coordinate system-level testing with Systems, Software, Hardware and Quality teams, mentoring peers and...

LivaNova PLC in Mirandola, Italy, is seeking a Senior System Verification Engineer to lead verification strategies across complex medical devices throughout the product lifecycle. You will translate requirements into comprehensive verification plans and coordinate system-level testing with Systems, Software, Hardware and Quality teams, mentoring peers and...

LivaNova PLC in Mirandola, Italy, is seeking a Senior System Verification Engineer to lead verification strategies across complex medical devices throughout the product lifecycle.You will translate requirements into comprehensive verification plans and coordinate system-level testing with Systems, Software, Hardware and Quality teams, mentoring peers and...

Jefferson Wells, divisione specializzata in ambito Healthcare & Life Sciences sta ricercando una figura di Senior Quality Systems Specialist per conto di una multinazionale biomedicale specializzata in dispositivi per dialisi e terapie renali, con stabilimento a Mirandola. Responsabilità Garantire la supervisione dello sviluppo e del mantenimento di...

Overview In this role you will lead system verification for complex medical devices, partnering with Systems Engineering, Software, Hardware, and Quality teams to ensure safety, performance, and regulatory compliance. You will translate system requirements into verification plans, execute tests, and maintain audit-ready documentation. You'll analyze...

Overview As a Quality Engineer, you will support product development, process validation, and quality improvements in a highly regulated medical device setting. You’ll collaborate with R&D, Manufacturing, and Quality to ensure compliance with ISO 13485, GMP, and other standards while driving safer, more reliable devices. Your work will influence design...

Overview In this role you will lead system verification for complex medical devices, partnering with Systems Engineering, Software, Hardware, and Quality teams to ensure safety, performance, and regulatory compliance. You will translate system requirements into verification plans, execute tests, and maintain audit-ready documentation. You'll analyze...

Overview In this role you will lead system verification for complex medical devices, partnering with Systems Engineering, Software, Hardware, and Quality teams to ensure safety, performance, and regulatory compliance. You will translate system requirements into verification plans, execute tests, and maintain audit-ready documentation. You'll analyze...