QA industrial compliance specialist (Saluggia)

QA industrial compliance specialist (Saluggia)

05 nov
|
Diasorin
|
Saluggia

05 nov

Diasorin

Saluggia

h3bObsessed by Science. Entrepreneurial by Nature. United by Purpose. /b /h3 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 pThrough the Quality Assurance function: to ensure that the industrial activities are fit for purpose, consistent and meet all internal and external requirements. /p ul lito ensure the adequacy and updating of Quality System with respect to the regulatory and quality requirements /li lito ensure labeling, IFU and any related documentation (e.g. changes, SOPs, specifications, attachments, etc.) are in compliance with the regulatory requirements /li /ul h3Key Duties And Responsibilities /h3 ul lito verify the application of the Quality Management System /li lito draft and review of standard operative procedures /li lito elevate to the line manager risks associated to his/her activities that could impact the QMS /li lito verify that procedures are properly established and applied to prevent non-conformity /li lito collaborate with the technical teams in the definition of the correct risk assessment on the product/processes /li lito support industrial departments in the process of requesting and applying the relevant Change /li lito evaluate the impact of the proposed Changes on its own field of competence /li lito manage the documentation to release the manufactured lots /li lito perform internal and external audits (in presence of appropriate certification) /li lito collaborate during audits conducted by external bodies to manage properly the team /li lito collaborate during internal audits /li lito support the correct process of review and release of labeling documents /li lito support the correct process of review and release of quality system documentation /li lito define actions for continuous improvement /li /ul h3Education, Experience, And Qualifications /h3 ul liDegree in scientific disciplines such as (but not limited to) Chemistry, Pharmacy, Biology, /li lior other professional qualification with previous experience in similar jobs. /li liAt least 2 year of Medical Device-IVD or chemical-pharmaceutical industry experience in similar position /li liKnowledge of quality and compliance management as well as GMP requirements and, as plus, requirements applicable to In Vitro Diagnostic Medical Devices. /li liKnowledge of the main current requirements applicable to IVD field. Use of Office pack. Risk management and related tools. /li liStrong verbal and written communication skills /li liSolid problem solving and analytical skills /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 liNative Italian and fluent English /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 € 35.117,32 /li liVariable compensation linked to the achievement of objectives /li /ul pActual pay is set on objective criteria: seniority, distinctive skills, scope of responsibility. /p 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

📌 QA industrial compliance specialist (Saluggia)
🏢 Diasorin
📍 Saluggia

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