PpAt Kedrion, we believe that innovation and care must go hand in hand. Our mission is to enhance lives through our dedicated work in the field of rare and ultra‑rare diseases. As a global leader with a passionate team of 5,200 employees, we collect and fractionate plasma to produce and distribute 38 vital medicines worldwide, establishing ourselves as the fifth largest player in the plasma‑derived products sector. /p h3Job Summary /h3 pWe’re looking for a motivated professional to cover the position of IT Digital Manufacturing Specialist to support the implementation, integration, and ongoing enhancement of digital solutions dedicated to Kedrion pharma Production, Quality, and MSD operations. /p pThe IT Digital Manufacturing Specialist operates within the IT Department and will be responsible for supporting the definition and execution of our company's digital strategy for Operations business area, leading cross‑functional initiatives and facilitating the organization’s adoption of innovative technologies. The job owner contributes to the identification of opportunities, to the modernization of processes based on a Data‑Driven approach, ensuring alignment with Global IT objectives and collaborating closely with all internal and external stakeholders. /p pThe position, in particular, takes charge of driving growth for Manufacturing Execution Systems and Manufacturing Operation Management (MOM), which will be essential in shaping the future of manufacturing and in delivering exceptional value to our Company, and of managing daily application support. /p h3What you’ll do /h3 ul liProactively contribute to foster innovation and identify opportunities for new digital solutions I4.0 and assess new digital initiatives for feasibility, business value, and impact. /li liFacilitate the digitalization of bGMP processes /b within Manufacturing, QC laboratories, QA systems, and MSD, while contributing to the technological roadmap for MES/MOM and Real‑Time Data Gathering projects. /li liWork together with business functions and external suppliers to implement and improve essential digital platforms such as bMES /b, MBR design, and the analysis of production processes, translating them into bmanufacturing automation /b logic. /li liArchitect and integrate end‑to‑end solutions involving MES and ensure compatibility with existing technologies. /li liCollaborate to implement bReal‑Time Data Tools /b and predictive tools (process monitoring, AI/ML models, real‑time dashboards). /li liTranslate business requirements into actionable IT solutions, providing technical guidance and leveraging extensive industry and product knowledge. /li liServe as a subject‑matter expert in manufacturing IT for MES and Real‑Time Data Tools, managing systems lifecycles, including planning, deliverable management, timeline management and stakeholder communication. /li liProactively support the integration between IT and OT solutions. /li liCollaborate with Global CSV Team for the validation of the implemented solutions. /li liGuarantee the expected level of service and adapt the solutions to be proposed and implemented based on the required level, through corrective and adaptive actions from time to time. /li /ul h3Qualifications and need‑to‑know /h3 ul liBachelor’s or Master’s degree in Engineering, Computer Science or STEM fields. /li li3+ years in Pharma / Biopharma, specializing in MES, complex projects, digitalization, and manufacturing technology. /li liAt least basic knowledge of LIMS, QMS. /li liIt is a plus, advanced skills in MES Werum Pas‑X and knowledge of Process Automation/DCS and data historians. /li liFamiliarity with 21 CFR Part 11 and ISA‑95 standards. /li liProfessional English proficiency (B2+). /li liProject Manager experience with project governance and performance monitoring; bPMP certification /b is a plus. /li liStrong stakeholder management, leadership, and change management skills in regulated settings. /li liExcellent communication, negotiation, and presentation abilities. /li /ul pThis announcement is addressed to applicants of both sexes (L. 903/77 - D.Lgs n. 198/2006) and also to those belonging to Protected Categories (L.68/99). /p /p #J-18808-Ljbffr