Wanted: Mes Business Analyst

Wanted: Mes Business Analyst - Detalhes da Vaga. ● Significant customization of Aveva MES is required to adapt it for the clients GXP/GMP processes in pharma, as the standard product is not fully suited to the manufacturing process, will need to do some custom development. ●This role supports a large-scale MES program across 26 sites, acting as a global business system owner with strong functional accountability for harmonizing manufacturing processes, shaping MES capabilities, and ensuring business alignment across implementations. ● Role: MES Global Business Analyst. ● Needs to have senior level MES skills, with at least 1 Aveva project. ● Focus is more from the business side but needs to be able to interact with the technical team and will need some hands on Aveva experience. ● Responsibilities:Production of project status reports and functional progress updates for MES deploymentsEscalation management for process, design, and deployment issues affecting MES implementationCoordination of cross-functional teams involved in MES design, testing, and rolloutSupport global business activities related to manufacturing execution, electronic batch records, and process standardizationSupport the global business application owner in functional maintenance, enhancement prioritization, and solution testing and governanceRequirements:At least 5-7 years of experience in OT/IT projects within manufacturing, including significant exposure to MES implementation as a business representative or functional leadStrong functional understanding of MES capabilities such as electronic batch records, recipe/workflow execution, material traceability, review by exception, and equipment status managementExperience translating site business needs into user requirements, process flows, and harmonized global solutionsExperience in GxP-regulated environments, ideally within pharmaceutical manufacturingGood knowledge of pharma manufacturing processes, including batch execution, dispensing, weighing, and quality-related process controlsExperience working in Agile or hybrid project delivery models is preferredKey Responsibilities:Collect user requirements from sites and drive standardization and harmonization of MES-supported manufacturing processesSupport the definition of core MES data structures such as Master batch records, materials, resources, and master dataReview functional solution design proposed by the system integrator and escalate gaps, risks, or misalignment with business needsMonitor and control solution definition across multiple parallel implementations to ensure consistency of core MES functionsOversee UAT preparation and execution, ensuring test scenarios adequately cover critical manufacturing and compliance processesAssess change impacts at site level, including process adoption, training needs, and local operational readinessExperience:Experience in MES implementation projects within regulated manufacturing environments, ideally in Pharma. Requisitos para participar do processo. ● . O que oferecemos.