About the Job

Company ContextSanofi's strategic direction is to standardize processes across sites, embrace digital transformation of its Manufacturing & Supply perimeter, simplify its current solution landscape, and leverage advanced technologies to bring business value.The MARS (MES Accelerated Roadmap @ Sanofi) program aims to implement Computer-assisted batch review, enabled by the definition and roll-out of a core Manufacturing Execution System (MES). This program will transform Sanofi plants, improving compliance, cost, and cycle time performance.Over recent years, Sanofi has deployed various Production sites across GBUs (multiple pharmaceutical processes, Weighing & Dispensing & full MES), with a second wave currently in motion. This represents a strategic opportunity for Manufacturing & Supply Transformation to:Design standardized end-to-end processes to generate business value and deliver best-in-class solutions to industrial sites, with high focus on electronic batch record management & review by exception processDeliver innovative "state of the art" tools enabling performance for manufacturing processesAllow new generation of deployment – more Agile & business centricMaintain robust and highly available solutions to operate industrial processes efficiently

Role OverviewThe MBR Developer is responsible for building, testing, and implementing Master Batch Records (MBRs) and related components within the Manufacturing Execution System (MES). You will ensure that MBR configurations align with the Core model and operational excellence standards while adhering to Sanofi Digital and Industrial standards for Processes, Applications, and Infrastructure environments.Working in close collaboration with MES Digital Product Configuration Manager, MES Digital Product Configuration Experts, MES Product Owner, MES installers/developers, Product lines, local digital teams, Business Process Owners, and Site modelers, you will contribute to the successful implementation of MES solutions across Sanofi manufacturing sites.

Systems & Processes in ScopeMain MES Systems:Siemens MES Opcenter Execution Pharma ProductSiemens Equipment logbook PharmaMain platform :MendixBusiness Processes Covered:Master data management (items, user rights, equipment, locations, work orders)Master batch record design & approval (including workflows)Master batch record review & approval (by Exception)Production executionInstructions for Operating TextWeighing & DispensingCommunication to equipment or SCADA systemsEquipment managementMaterial flow managementTraceability / GenealogyLabellingReportingInterface with ERP, quality, logistics & shopfloor systems (LIMS, Documentation, Deviation management, Serialization, eOEE)

Main Responsibilities

Business AlignmentUnderstand business requirements and contribute to building & testing solutionsSupport the implementation of appropriate services to ensure optimal allocation of available capabilitiesContribute to end-to-end business process analysis including integration with partner systemsCollaboration & Skills DevelopmentContribute to Digital skills development within your domainCollaborate effectively in a matrix environmentDelivery & Quality of ServicesBuild and test MBRs, Process Instructions, blocks, and templates according to specifications provided by Digital Product Configuration Experts/ following established guidelinesDevelop and maintain test scripts for MBR validationFollow established build and test methodologies by adopting GxP validationsPerform or participate in regular MBR reviews for sitesConfigure & implement core solutions as close to standard market solutions as possibleEnsure solution builds are aligned with user requirements & core modelEnsure technical solutions comply with recommendations for Quality, Security, and AccessibilitySupport the proper deployment of core solutionsEnsure standards of Platform Management (Release, solution documentation, testing) are followedContribute to the on-time delivery of projectsSupport impact analysis of configuration changesTroubleshoot and resolve technical issues during MBR implementationDocument technical aspects of MBR configurationsSupport system testing and validation activitiesSupport the Implementation of configuration changes following change control proceduresManage incidents & corrective/preventive actionsQuality and ComplianceTrack and report on established KPIs for quality of serviceEnsure all configurations meet GMP requirements and data integrity standardsMaintain configuration documentation in alignment with validation requirements

About You

Experience & Knowledge3-5 years work experience in Digital Manufacturing/MES specifically on Siemens OPCenter Execution Pharma and Siemens Equipment logbookMES experience with relevant solutions/ modules/functionalitiesExperience working in multicultural/matrixed environmentsExperience & understanding of core product/model conceptExperience working in industrial plants is preferred but not mandatory

Technical SkillsKnowledge of MES solutions: Siemens OPCenter Execution Pharma and Siemens Equipment logbookKnowledge of pharma industry regulatory context (GxP)Knowledge of Digital technologies & conceptsBeginner knowledge/ experience on MendixKnowledge of Automation layer (SCADA, DCS, PLCs) is a plusKnowledge of scripting (VB/.Net) and JSON is a plusSoft SkillsAccountability and reliabilityGood mindset - quick learner, proactive, willing to apply change managementCollaboration and good team playerAbility to deal with ambiguous situationsFocus on value delivery, with the ability to work on solution build and testing and proactiveness within the assigned scopeKnowledge of Agile methodologiesEducationEngineering degree in Computer Science or related fieldLanguageFluent in English, other languages are a plusWorking EnvironmentTravel requirement: Occasional travel to manufacturing sitesGlobal, matrix organization environmentMust be able to work effectively across different time zones and cultures

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!