Product Development Technical Experts

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 Supports project activities for assay development of LIAISON® family for the following product categories: - new product; - new generation of an already existing product; - change of already existing product (change of technology / change of critical supplier). Help with the definition of the product and process risks associated with the product development activities, in collaboration with the site ToT groups. Acts in compliance with Product Design requirements and Product Development Master Plan. Key Duties and Responsibilities He/She helps with the definition of master formulas of kit components and assay scheme of LIAISON® prototypes. He/She updates the Team Managers on progression of activities from technical and timelines perspective. He/She helps with the verification of critical aspects and requirements of bench prototypes in compliance with internal regulations (GOP-SOP) and external and internal quality standards. He/She helps witht the definition of product claims in compliance with internal regulations (GOP-SOP) and external and internal quality standards He/She helps with project documentation. He/She collaborates to panels and raw material definition required for project activities and industrialization phase. He/She collaborates with DiaSorin Research Center during the evaluation of prototypes and raw materials transferred to DiaSorin sites. He/She collaborates with the Regulatory departments of DiaSorin sites for the drafting the pre-submission documents (pre-IDE) and the submission documents to notified bodies. He/She collaborates on technical analysis for complaints and / or trends of product performances. He/She supports the activities assigned to the Laboratory Staff of the Team. Education, Experience, and Qualifications University degree in a scientific discipline. Professional experience: A) Two year experience (minimum) in diagnostic or pharmaceutical Companies. B) Knowledge of mandatory requirements for in vitro "Diagnostic Medical Devices" Skilled with Office Tools (word, Excel) Basic Statistical analysis with MiniTab or equivalent softwares DoE basic skills Proactive, flexibility, able to support decisions and communications. Able to act within timely manner and precision for the team. Fluent in written and spoken Italian and English.