Global Software Design and Development Immuno Engineer
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.
- 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
- 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.
- Investigate anomalous and/or uncommon situations and participate in risk assessments.
- Interact with other development areas within the team (e.g. 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.
- Perform assigned tasks in accordance with applicable safety regulations and instructions; 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.
- Previous experience in IVD (In Vitro Diagnostics), highly regulated FDA environments, and/or the biotechnology industry is highly appreciated.
- 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.
- 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 accuracy, comprehension of technical issues, and ability to communicate them effectively across all levels and groups.
- Strong problem‑solving and decision‑making capabilities, with effective negotiation and analytical skills focused on results and project timelines.
- Interdisciplinary thinking and high-quality awareness.
- Ability to collaborate effectively with other SD&I leads in a team‑oriented environment.
- High commitment and willingness to learn.
- Positive, proactive, and open‑minded attitude, with willingness to engage and lead others.
- Strong commitment to the success of all SD&I projects and initiatives.
- Fluent spoken and written Italian and English
- Travels may be required
- 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
- 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
Offerta di lavoro pubblicata 2 mesi fa
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