Ph3Clinical Affairs Technical Specialist /h3 pPublished on: Jan 8, 2026 /p pJob Category: Research Development /p pEmployment type: Regular Full Time /p h3Diasorin 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. /h3 h3Our 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". /h3 h3bWhy Join Diasorin? /b /h3 h3Impactful 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. /h3 h3Global 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. /h3 h3Diverse 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. /h3 h3Join 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. /h3 h3Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact! /h3 pbJob Scope /b /p ul liWithin 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. /li liContributes to the planning, conduct and evaluation of clinical performance studies. /li /ul pbKey Duties and Responsibilities /b /p ul liPerform experimental testing activities for the verification and validation of the clinical performance of newly developed immunodiagnostic products or existing products. /li liPerform experimental testing on competitor products for the characterization of clinical samples and performance comparisons. /li liGuarantee the proper conservation of clinical samples and the archiving of the related documentation, make them available for the execution of experimental tests or shipment to testing centers. /li liSupport the shipping activities of immunoassay prototypes to clinical validation centres, with the related documentation. /li liKeep 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. /li liGuarantee the correct compilation and availability of product documentation relating to the assigned activities. /li liCollaborate in technical analyzes in the event of complaints and/or trends in non compliant performance. /li liCarry out activities in the various phases of the project according to current laws, internal regulations, and external and internal Quality regulations. /li liCollaborate 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. /li liParticipate in activities necessary to initiate, conduct, and monitor clinical performance studies. /li /ul pbEducation, Experience, and Qualifications /b /p ul liBachelor’s degree or a professional qualification of an equivalent or higher standard, scientific and technical. /li liMinimum 3 years work experience in the health care and science industry, preferably with diagnostic, medical devices or pharmaceutical Companies, with knowledge of relevant device technologies and related design processes. /li liKnowledge of the legislation about the clinical performance of immunodiagnostic products. /li liAbility to work independently while respecting roles. /li liAbility to relate with external and internal interfaces. /li liGood attitude to work in team. /li liAbility to express oneself clearly verbally and in writing. /li liPrecision and attention to detail. /li liFlexibility and proactiveness. /li liAvailability to travel (not extensively). /li liGood spoken and written English. /li /ul h3Diasorin 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. /h3 h3In 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. /h3 h3Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at or to request an accommodation. /h3 h3The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. /h3 h3Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations. /h3 h3Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations. /h3 h3This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department. /h3 /p #J-18808-Ljbffr