pObsessed by Science. Entrepreneurial by Nature. United by Purpose. /p pDiasorin 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. /p pAs 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. /p pWhen you join Diasorin, you are not just filling a role. You are helping build what comes next. /p h3Why Join Diasorin /h3 ul liBuild What Matters Take ownership, challenge the status quo, and contribute directly to solutions that improve patient care worldwide. /li liInnovate with Agility at a Global Scale Work in an entrepreneurial environment that enables speed, collaboration, and global impact. /li liGrow in a People-Centered Culture Thrive in a culture that values accountability, inclusion, and continuous development. /li /ul h3Job Scope /h3 ul liDevelop and maintain a Quality management system in line with the regulatory and mandatory requirements applicable to Medical Device and IVD (including ISO 9001, ISO 13485, cGMP, IVDR ecc) through existing and new documentation /li liEnsure that all relevant documents are updated, revised and modified in accordance with quality management system requirements /li liSpreads awareness of quality management system to all levels of the company /li liSpread, through appropriate trainings, a culture of continuous improvement and good manufacturing practice across the company /li liCooperate with other functions to ensure that new projects and processes are in compliance with all internal and external requirements. /li liDetermine, through planned internal audits, whether the Quality management system is conform to the applicable requirements and effectively implemented and maintained /li liSupport Subsidiaries,



Distributors and customers providing required product documentation /li /ul h3Key Duties And Responsibilities /h3 ul liEnsure that all relevant documents are updated, revised and modified in accordance with quality management system requirements /li liEnsure that changes inside DSI are evaluated and managed in accordance with quality management system requirements /li liSupport Product Development dept providing documentation for new products /li liSupport the Regulatory dept providing documentation in compliance with the needs of external certification bodies /li liIn company quality projects ensure that all activities are performed in compliance with quality a system requirements /li liEnsure that training activities are managed and recorded according to the quality requirement in order to give evidence that personnel is adequately trained for a specific job. /li liPerform training personnel about the requirements of QMS and cGMP. /li liManage internal audit ensuring that they are performed at regular intervals and that all nonconformities raised during audits are effectively corrected /li liGive support to second and third party audits /li liProvide product documentation (i.e certificates od Analysis, certificate of cornformance, ISO certificate ecc…) upon customer requests or for commercial purposes /li /ul h3Education, Experience, And Qualifications /h3 ul liDegree in scientific or technical disciplines. /li liAt least one year experience in similar or equivalent positions in chemical/pharmaceutical or medical device industries, or experience in the production/quality control of medical devices. /li liFamiliarity with Office programs such as Excel, PowerPoint, and Word /li liStrong verbal and written communication skills /li liSolid problem solving and analytical skillsSolid interpersonal skills,



including ability to negotiate and influence without authority /li liStrong communication and interpersonal skills with ability to work well in a high pressure environment /li liStrong competency in Customer Focus and Driving for Results /li liFluent knowledge of the English language /li /ul h3What We Offer /h3 ul liPermanent employment contract /li liClassification under the Chemical-Pharmaceutical CCNL (Italian national collective bargaining agreement) /li liGross annual base salary from € 33.598,46 /li liVariable compensation linked to the achievement of objectives /li liActual pay is set on objective criteria: seniority, distinctive skills, scope of responsibility. /li /ul pAt Diasorin, we are committed to supporting the well-being of our employees every day - which is why we complement compensation with a comprehensive set of benefits: /p ul liFree canteen /li liFeel Good - Diasorin for You: a dedicated well-being program offering initiatives, services, and opportunities designed to support you every day /li liA benefits package guaranteed by the Chemical-Pharmaceutical CCNL, including a supplementary pension fund and supplementary healthcare coverage /li liCompany welfare plan offering flexible benefits you can tailor to your needs /li /ul pDiasorin 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. /p pDiasorin 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, disability, protected veteran status, or any other characteristic protected by applicable law. /p pThis 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. /p pIndividuals 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. If assistance is required, please contact /p #J-18808-Ljbffr

📌 Quality System Specialist (Saluggia)
🏢 Diasorin
📍 Saluggia