We are looking for a **Validation Specialist **to join the Quality Validation team based in **Piombino Dese (PD).** Stevanato Group is an Italian but multinational manifacturing company. We develop and produce **drug containment solutions in glass **and plastics. The main production process is the the **processing of the glass tube by forming **and the subsequent **cleaning **and **sterilization **of the container using **highly automated machinery **. The function of Validation team is to ensure the approval and validation of all production processes and supporting IT systems, as well as utilities, test methods, equipment and cleaning processes, producing a product that meets all applicable internal and regulatory requirements. The function is part of a corporate team, with **multi-site responsibility **. The figure will be involved in the following main activities: - Develop, execute and review documents related to Validation activities (e.g. validation plan, protocol, report,



technical document, risk assessment), including management of deviations;
- Execute and/or coordinate assigned Validation activities related to Qualification and Validation area;
- Management of Change control related to production processes as assigned;
- Interfacing with suppliers/internal companies within the group to collect the information necessary for the preparation and/or review of protocols;
- Assist during FAT, SAT and IOQ with Engineering and Supplier;
- Participate at workshops/projects for continuous improvement and global standardization initiatives within organization;
- Support maintenance of document GMP archive including the responsibility for correct consultation, data collection, retrieval and returning of documents and archiving process.

📌 Quality Validation Specialist (8760) (Piombino Dese)
🏢 STEVANATO GROUP
📍 Piombino Dese