Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world. Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist." Why Join Diasorin? **Impactful Work**: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world. **Global Reach & Innovation**: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry. **Diverse and Inclusive Culture**: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive. **Join Our Team**: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward. Job Scope Within the assigned projects, he/she participates in all experimental testing activities for the verification and clinical validation of newly developed or existing immunodiagnostic products,



in compliance with the established requirements, the assigned deadlines and the applicable Quality System procedures. Contributes to the planning, conduct and evaluation of clinical performance studies. Key **Responsibilities**:
Performs experimental testing activities for the verification and validation of the clinical performance of newly developed immunodiagnostic products or existing products. Performs experimental testing on competitor products for the characterization of clinical samples and performance comparisons. Guarantees the proper conservation of clinical samples and the archiving of the related documentation, makes them available for the execution of experimental tests or shipment to testing centers. Supports the shipping activities of immunoassay prototypes to clinical validation centers, with the related documentation. Keeps the Manager and the work team updated on the progress of the assigned activities, both from a technical point of view and about compliance with progress deadlines. Guarantees the correct compilation and availability of product documentation relating to the assigned activities. Collaborates in technical analyzes in the event of complaints and/or trends in non-compliant performance. Carry out activities in the various phases of the project according to current Iaws, internal regulations, and external and internal Quality regulations.



Collaborates in drafting protocols for clinical performance studies, in the analysis of results and in the drafting of final reports, for the verification and validation of clinical performances. Participates in activities necessary to initiate, conduct, and monitor clinical performance studies. Education, Experience, and Qualifications Bachelor’s degree or a professional qualification of an equivalent or higher standard, scientifical and technical. Ability to work independently while respecting roles. Ability to relate with external and internal interfaces. Good attitude to work in team. Ability to express oneself clearly verbally and in writing. Precision and attention to detail. Flexibility and proactiveness. Knowledge of the legislation about the clinical performance of immunodiagnostic p roducts. Good proficiency in both written and spoken English Availability to travel (not extensively). What we offer Receive a competitive salary and benefits package as you grow your career at DiaSorin. Join our team and discover how your work can impact the lives of people all over the world. Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire. The above job description is intended to describe the general content, identify the essential function

📌 Clinical Affairs Technical Specialist (Saluggia)
🏢 Diasorin
📍 Saluggia