Mes Configuration Expert Opcenter Execution Pharma - Sanofi

OverviewIn this role you will design and configure Siemens Opcenter Execution Pharma to support Sanofi’s global MES landscape.You will align local configurations with the Core model and industrial standards, working closely with MES teams to deliver scalable, compliant manufacturing solutions.You’ll tackle cross-site process integration, data flows, and documentation, contributing to operational excellence.This position offers impact across multiple sites, shaping how manufacturing executions enable efficiency and quality at scale.ResponsabilidadesUnderstand and translate business requirements into scalable MES configurations and processesDesign, build and review Master Batch Records (MBR) and related workflows, aligning them with core practicesConfigure core MES solutions close to market standards and state-of-the-art practicesLead on-time project delivery while ensuring cost-effective, compliant solutionsSupport incident management and corrective/preventive actions for MES componentsCollaborate with site modelers, MES leads, and cross-functional teams on design reviews and deploymentMaintain alignment with Quality, Security, and accessibility standardsProvide training and knowledge transfer to manufacturing sitesRequisitos principales5+ years in Digital for Manufacturing with MES experience, preferably Siemens Opcenter Execution PharmaStrong knowledge of MES, MBRs, and review-by-exception processesPharma industry regulatory context (GxP) knowledgeExperience with integration to ERP, shopfloor systems, automation layersUnderstanding of SCADA/DCS/PLCs and industrial protocolsScripting experience (VB/.Net) and validation knowledgeAccountability and reliabilityCustomer-driven mindsetFast learner and proactive with change managementSiemens Opcenter Execution PharmaMaster Batch Record design and approvalsGxP validation

Requisitos principales5+ years in Digital for Manufacturing with MES experience, preferably Siemens Opcenter Execution Pharma Strong knowledge of MES, MBRs, and review-by-exception processes Pharma industry regulatory context (GxP) knowledge Experience with integration to ERP, shopfloor systems, automation layers Understanding of SCADA/DCS/PLCs and industrial protocols Scripting experience (VB/.Net) and validation knowledge Accountability and reliability Customer-driven mindset Fast learner and proactive with change management Siemens Opcenter Execution Pharma Master Batch Record design and approvals GxP validation