Quality System Specialist (Saluggia)

Quality System Specialist (Saluggia)

20 ott
|
Diasorin
|
Saluggia

20 ott

Diasorin

Saluggia

pSelect how often (in days) to receive an alert: /ph3Quality System Specialist /h3pPublished on: Oct 16, 2026 /ppJob Category: Operations /ppEmployment type: Regular Tempo pieno /ph3bObsessed by Science. Entrepreneurial by Nature. United by Purpose. /b /h3pDiasorin 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. /ppAs 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. /ppWhen you join Diasorin, you are not just filling a role. You are helping build what comes next. /ph3bWhy Join Diasorin /b /h3ulliBuild What Mattersbr/Take ownership, challenge the status quo, and contribute directly to solutions that improve patient care worldwide. /liliInnovate with Agility at a Global Scalebr/Work in an entrepreneurial environment that enables speed, collaboration, and global impact. /liliGrow in a People-Centered Culturebr/Thrive in a culture that values accountability, inclusion, and continuous development. /li /ulpbJob Scope /b /pulliDevelop 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 /liliEnsure that all relevant documents are updated, revised and modified in accordance with quality management system requirements /liliSpreads awareness of quality management system to all levels of the company /liliSpread, through appropriate trainings, a culture of continuous improvement and good manufacturing practice across the company /liliCooperate with other functions to ensure that new projects and processes are in compliance with all internal and external requirements. /liliDetermine, through planned internal audits,



whether the Quality management system is conform to the applicable requirements and effectively implemented and maintained /liliSupport Subsidiaries, Distributors and customers providing required product documentation /li /ulpbKey Duties and Responsibilities /b /pulliEnsure that all relevant documents are updated, revised and modified in accordance with quality management system requirements /liliEnsure that changes inside DSI are evaluated and managed in accordance with quality management system requirements /liliSupport Product Development dept providing documentation for new products /liliSupport the Regulatory dept providing documentation in compliance with the needs of external certification bodies /liliIn company quality projects ensure that all activities are performed in compliance with quality a system requirements /liliEnsure 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. /liliPerform training personnel about the requirements of QMS and cGMP. /liliManage internal audit ensuring that they are performed at regular intervals and that all nonconformities raised during audits are effectively corrected /liliGive support to second and third party audits /liliProvide product documentation (i.e certificates od Analysis, certificate of cornformance, ISO certificate ecc…) upon customer requests or for commercial purposes /li /ulpbEducation, Experience, and Qualifications /b /pulliDegree in scientific or technical disciplines. /liliAt 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. /liliFamiliarity with Office programs such as Excel, PowerPoint, and Word /liliStrong verbal and written communication skills /liliSolid problem solving and analytical skills /liliSolid interpersonal skills,



including ability to negotiate and influence without authority /liliStrong communication and interpersonal skills with ability to work well in a high pressure environment /liliStrong competency in Customer Focus and Driving for Results /liliFluent knowledge of the English language /li /ulpbWhat we offer /b /pulliClassification under the Chemical-Pharmaceutical CCNL (Italian national collective bargaining agreement) /liliGross annual base salary from € 33.598,46 /liliVariable compensation linked to the achievement of objectives /liliActual pay is set on objective criteria: seniority, distinctive skills, scope of responsibility. /li /ulpAt 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: /pulliFree canteen /liliFeel Good – Diasorin for You: a dedicated well-being program offering initiatives, services, and opportunities designed to support you every day /liliA benefits package guaranteed by the Chemical-Pharmaceutical CCNL, including a supplementary pension fund and supplementary healthcare coverage /liliCompany welfare plan offering flexible benefits you can tailor to your needs /li /ulpDiasorin 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. /ppDiasorin 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. /ppThis 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. /ppIndividuals 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

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