Quality Validation Specialist Lazio

Quality Validation Specialist
Roma
Lazio, Lazio

Social network you want to login/join with: Quality Validation Specialist, Province of Latina Client: Location: Province of Latina, Italy Job Category: Other EU work permit required: Yes Job Reference: bb282dfb915b Job Views: 9 Posted: 02. 03. 2025 Expiry Date: 16. 04. 2025 Job Description: Job Description We are looking for a Validation Specialist to join the Quality Validation team based in Cisterna di Latina (LT). Stevanato Group is an Italian but multinational manufacturing company. We develop and produce drug containment solutions in glass and plastics. The main production process is the processing of the glass tube by forming and the subsequent cleaning and sterilization of the container using highly automated machinery. The function of the 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: VALIDATION MANAGEMENT Executes the qualification and validation activities in order to achieve the validation targets according to the approved plan, guaranteeing compliance with applicable standards. Supports the leader in the definition of qualification and validation activities, ensuring compliance of the quality management system with applicable standards and requirements. Provides timely and accurate validation documents, monitoring third-party reports for final submission. Participates alongside the Commercial Team to carry out new projects, ensuring technical assistance and validation, as well as with the R&D Team to define appropriate processes to guarantee the quality and reliability of the products. GUIDELINES AND PROCEDURES Contributes to cascade accurate and up-to-date information related to regulations, customer requirements, and other applicable standards to the team and other functions involved in the processes. Supports the validation practices definition, ensuring inclusion within the relevant quality management system. Provides technical support to other functions to ensure full application of the relevant quality management system regarding validation processes. QUALITY AUDIT MANAGEMENT Participates in audit sessions and customer technical meetings to provide accurate and timely technical services and support, executing corrective and preventive actions assigned while working closely with involved teams. REPORTING AND MONITORING Elaborates appropriate reports to monitor KPIs related to validation and meet internal and external needs, highlighting deviations and critical issues, and proposing actionable initiatives to achieve effective resolution. Qualifications Scientific Master's Degree 2 years' experience in Validation in a multinational company (preferably in a pharmaceutical and medical devices company) Knowledge of internal audit processes and techniques. Knowledge of applicable regulatory standards and global manufacturing practices. Legal and standard requirements linked to the relevant applicable standards. Familiarity with IT tools. Availability to travel within the national territory is required. J-18808-Ljbffr