ppExperteer Overview In this role you will support the mRNA Manufacturing Process Unit to ensure compliant, efficient production of mRNA Drug Substances and Drug Products. You work as a SME, coordinating projects and changes across site functions to keep operations running smoothly. You’ll address process issues, drive CAPA and deviation closure, and support qualification activities. This position offers leadership exposure in a dynamic, outcomes-driven environment with a focus on continuous improvement and collaboration. /ph3Retribuzione / Benefits /h3ulliManage facility, equipment, documentation and process issues with cross‑functional teams (Maintenance, Engineering, MSAT, Quality) /liliSupport deviation management, identify root causes, ensure on‑time CAPA closure /liliOpen and review Deviation, CAPA and Change Control records /liliPrepare and review manufacturing documentation (SOPs, Protocols, Reports, Risk Assessments) /liliWork with MSAT to define equipment and consumable specifications, URS,



and drawings /liliOversee new implementations/modifications of the mRNA process unit, coordinating across functions /liliPlan and monitor commissioning, qualification activities (externally and internally) /liliLead CAPA and Change Control implementations /liliParticipate in on‑site client visits and audits related to the facility /liliPromote trainings and process courses within the mRNA business /liliPursue continuous improvement and cost‑saving projects /li /ulh3Responsabilità /h3ulli3+ years GMP manufacturing experience with strong quality mindset /liliSolid knowledge of upstream and downstream processes for mRNA Drug Substances and Drug Products /liliStrong communication and leadership skills /liliProactive, prevention‑focused problem solving /liliTeam‑building capability /liliItalian and Fluent English /liliYellow or Green Belt Certification a plus /li /ul /p #J-18808-Ljbffr

📌 Manufacturing & Mbr Specialist, Mrna Manufacturing (Monza)
🏢 Experteer Italy
📍 Monza