Obsessed by Science. 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. Innovate with Agility at a Global Scale Work in an entrepreneurial environment that enables speed, collaboration, and global impact.

Job Scope The Global Software

Design and Development Engineer will provide technical leadership, along with individual contributions, to the development of software required by Diasorin to satisfy the needs of customers, assay developers, instrument manufacturers, and service departments, with regard to both new instrument development and the improvement of existing instruments: through a motivational, professional, quality‐driven, and proactive attitude with the goal of building solid corporate know‐how, to provide Diasorin customers with the highest quality and innovation in products and services Key Duties And Responsibilities Design, create, review, and update software specifications and software designs derived from user requirements, in collaboration with multi‐disciplinary project teams. Create, review, and perform software unit test plans and protocols. Create and maintain technical documentation related to software and firmware under development or maintenance, in compliance with Diasorin procedures.

Troubleshooting of software under development and support software releases, serving as a point of contact for other groups. Hardware, Assay Integration) to assess feasibility of proposed implementations and solutions. Collaborate with other Company functions to provide technical expertise and support problem solving.

Ensure compliance with the Quality Management System, Company Policies, and Corporate Procedures, working closely with Quality, Regulatory, and Clinical groups. correct unsafe work habits and practices and/or report any condition that may be detrimental to employee safety and health. Continue personal development in software programming,



software best practices, and in‐depth understanding of requirements for developing medical device software. Education, Experience, And Qualifications Master's Degree in Computer Science, Engineering, Physics, or Mathematics.

Experience 4+ years of experience in computer programming, including at least 3 years of post‐Master's software development. Previous experience in IVD (In Vitro Diagnostics), highly regulated FDA environments, and/or the biotechnology industry is highly appreciated.

Technical Competencies

Apply knowledge of Microsoft Windows technologies, software design principles, and secure coding approaches to design high‐quality software architectures for new applications.

Experience developing and releasing software applications with C++ or C# and .NET is required. Proficiency in debugging tools and understanding of unit‐testing methodologies.

Experience with version control systems (e.g. Git). Knowledge of iterative development models such as Agile/Scrum. Ability to create documentation, manuals, and detailed sets of instructions, including algorithms in pseudocode and computer programs. Understanding of cybersecurity principles and best practices is desirable. Knowledge or aptitude in cloud development, AI, and Machine Learning is desirable. Knowledge of the IEC 62304, GMP (Good Manufacturing Practice) is appreciated.

Skills Provide technical leadership and coaching to a software development team to motivate and drive the team to success. Organize, distribute, and oversee implementation tasks. Strong problem‐solving and decision‐making capabilities, with effective negotiation and analytical skills focused on results and project timelines.

Ability to collaborate effectively with other SD&I; leads in a team‐oriented environment.



Strong commitment to the success of all SD&I; projects and initiatives. Requested competencies and skills may vary depending on seniority Languages Fluent spoken and written Italian and English Travel availability Travels may be required HYBRID WORK What We Offer Permanent employment contract Classification under the Chemical-Pharmaceutical CCNL (Italian national collective bargaining agreement) Gross annual base salary from € 41.225,80 Variable compensation linked to the achievement of objectives Actual pay is set on objective criteria: seniority, distinctive skills, scope of responsibility.

Benefits Free canteen Feel Good - DiaSorin for You: a dedicated well-being program offering initiatives, services, and opportunities designed to support you every day A benefits package guaranteed by the Chemical-Pharmaceutical CCNL, including a supplementary pension fund and supplementary healthcare coverage Company welfare plan offering flexible benefits you can tailor to your needs Diasorin is committed to building a workplace where people feel empowered to contribute ideas, take ownership, and grow their careers. We believe diverse perspectives strengthen innovation and help us deliver meaningful impact for patients and customers worldwide. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by applicable law.

This posting and recruitment process are subject to applicable local laws and regulations in the country where the position is located. Additional employment disclosures, candidate rights, and employment conditions may apply based on local jurisdiction. xrdztoy Individuals hired will be required to verify identity and eligibility to work and may be subject to a background check and drug screening where permitted by law. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities during the application process.

📌 Global Software Design and Development Immuno Engineer (Torino)
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📍 Torino