Requirements: English
Company: Stevanato Group
Region: Latina , Lazio
We are looking for a Validation Specialist to join the Quality Validation team based in Cisterna di Latina (LT).Stevanato Group is an Italian multinational manufacturing company. We develop and produce drug containment solutions in glass and plastics.The main production process involves the processing of glass tubes through forming, followed by cleaning and sterilization of the containers using highly automated machinery.The Validation team is responsible for the approval and validation of all production processes, supporting IT systems, utilities, test methods, equipment, and cleaning processes, ensuring the product meets all internal and regulatory requirements. The team operates across multiple sites within the corporate structure.The successful candidate will be involved in the following main activities:VALIDATION MANAGEMENTExecute qualification and validation activities to meet targets according to the approved plan, ensuring compliance with applicable standards.Assist in defining qualification and validation activities to ensure the quality management system complies with standards and requirements.Provide accurate validation documentation and monitor third-party reports for review and submission.Collaborate with the Commercial and R&D teams on new projects to ensure technical assistance, validation, and process definition for product quality and reliability.GUIDELINES AND PROCEDURESContribute to updating and disseminating information related to regulations, customer requirements, and standards.Support the definition of validation practices and incorporate them into the quality management system.Provide technical support to ensure proper application of validation processes across functions.QUALITY AUDIT MANAGEMENTParticipate in audits and customer technical meetings, providing technical support and executing corrective actions as needed.REPORTING AND MONITORINGDevelop reports to monitor validation KPIs, identify deviations and issues, and propose corrective actions for resolution.QualificationsMasters Degree in a scientific fieldAt least 2 years of validation experience in a multinational, preferably in the pharmaceutical or medical devices industryKnowledge of internal audit processes and techniquesUnderstanding of applicable regulations, standards, and global manufacturing practicesLegal and standard compliance knowledge related to standardsProficiency with IT toolsWillingness to travel within the country is required.#J-18808-Ljbffr