17 ott - Carisio
Diasorin
Obsessed by Science. Entrepreneurial by Nature. United by Purpose.
Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions, advancing science to improve patient outcomes worldwide. For more than 50 years, we have combined scientific rigor with an entrepreneurial mindset, operating with a strong commitment to innovation, accountability, and results to deliver trusted diagnostic solutions.
As the Diagnostics Specialist, Diasorin continuously invests in research, technology, and people. Guided by our values of operational excellence, customer focus, and teamwork, we empower teams to think boldly, act decisively, and transform ideas into meaningful impact across one of the industry’s broadest specialty diagnostic portfolios.
When you join Diasorin, you are not just filling a role. You are helping build what comes next.
Why Join Diasorin
• Build What Matters
Take ownership, challenge the status quo, and contribute directly to solutions that improve patient care worldwide.
• Innovate with Agility at a Global Scale
Work in an entrepreneurial environment that enables speed, collaboration, and global impact.
• Grow in a People-Centered Culture
Thrive in a culture that values accountability, inclusion, and continuous development.
Job Scope
• Develop and maintain a Quality management system in line with the regulatory and mandatory requirements applicable to Medical Device and IVD (including ISO 9001, ISO 13485, cGMP, IVDR ecc) through existing and new documentation
• Ensure that all relevant documents are updated, revised and modified in accordance with quality management system requirements
• Spreads awareness of quality management system to all levels of the company
• Spread, through appropriate trainings, a culture of continuous improvement and good manufacturing practice across the company
• Cooperate with other functions to ensure that new projects and processes are in compliance with all internal and external requirements.
• Dete
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