Descripción de la oferta
Overview
In this role you design, build and govern global MES configurations (Werum PAS-X and Opstrakker) to align with the Core model and Sanofi standards. You collaborate with MES product and site teams to deliver compliant, scalable MES solutions that drive manufacturing efficiency. You work across processes, systems and infrastructure to enable lifecycle governance, risk control, and continuous improvement. Your work supports sites in solving issues and advancing digital manufacturing capabilities in a complex, multinational environment.
Compensaciones / Beneficioshybrid work (#LI-Hybrid)Barcelona Hubbenefit programsopportunities for international collaboration
ResponsabilidadesTranslate business requirements into scalable MES designs aligned with the Core ModelDesign and build Master Batch Records, MBR workflows and related templatesConfigure core solutions close to market standards and best practicesLead on-time delivery of projects and ensure robust, cost-effective solutionsParticipate in design reviews, MBR reviews, and incident/problem managementEnsure solutions comply with Quality, Security and Accessibility standardsMonitor performance indicators and ensure correct platform management processesProvide functional/technical training and transfer knowledge to sites
Requisitos principales5+ years in Digital for Manufacturing, especially MES (Werum PAS-X and Opstrakker)Strong MES knowledge and pharma industry regulatory context (GxP)Experience with integration to ERP, shopfloor, labelling, and mobile technologiesKnowledge of Automation layer (SCADA, DCS, PLCs) and scripting (VB/.Net)Experience with reporting tools (Power BI) and Cloud (Azure) is a plusMaster Batch Record design/Review by ExceptionProject management experience is a plusAccountability and reliabilityCustomer-driven mindsetFast learner and proactive in change managementWerum PAS-X (Körber)Opstrakker (elogbook/eforms)Master Batch Record and Review by Exception processes
