About the JobCompany 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 efficientlyRole Overview:The MES DevOps Manager is responsible for leading the delivery, design/ build/ implementation and continuous enhancement of global end-to-end Manufacturing Execution System (MES) solutions at Sanofi. This role focuses on team mgt/leadership, technical mgt/expertise, and delivery excellence to ensure MES configurations meet the needs of Sanofi's manufacturing operations while adhering to quality, regulatory, and cybersecurity requirements. The manager will manage a team (functionally, technically and administratively) of MES DevOps Engineers and MBR developers, take the ownership/ leadership of technical delivery of the team to answer to the requirements of manufacturing sites and align with the expectations of the product owner (Werum Pas-X, Opstrakker) and capability manager.Main MES Systems:Systems & Processes in ScopeWerum PAS-X Product (Korber)Opstrakker (elogbook/eforms)Business 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)Templates for elogbook (Opstrakker)Production executionWeighing & DispensingCommunication to equipment or SCADA systemsEquipment managementMaterial flow managementTraceability / GenealogyLabellingReportingInterface with ERP, quality, logistics & shopfloor systems (LIMS, Documentation, Deviation management, Serialization, eOEE)Main Responsibilities:Team Leadership and Management:Lead and manage a team of MES DevOps Engineers and MBR developersFacilitate onboarding and integration of team members as they join the organizationDrive knowledge building and skill development within the team. Foster a culture of continuous learning and best practice sharing among team membersEnsure team members are prepared and able to travel to Sanofi industrial sites globally (Europe, NA, Asia) where MES is in use. And ensure team members are developing a closed partnerships with sites users & business system owners to guarantee a full understanding of business requirements, stakes, challenges, constraints & ultimately build efficient solutionsManaging the priorities of the team, Facilitating resource allocation and management for various MES projects across Digital Manufacturing & SupplyTaking the ownership/ leadership of technical delivery of the team, ensuring knowledge transfer, and contributing to operational excellence to answer to the requirements of manufacturing sites and align with the expectations of the product owner (Werum Pas-X, Opstrakker) and capability manager.Technical Expertise and Team Development:Assess and enhance the technical capabilities of the teamIdentify skill gaps and implement targeted training and development programsEstablish mentoring relationships to accelerate team members' growth and expertiseCreate a collaborative environment that encourages innovation and problem-solvingEnsure the team stays current with evolving MES technologies and industry best practicesDevelop leadership & accountability at each individual levelTechnical Configuration and Solution Design:Oversee the design and build of MES configurations, ensuring alignment with standard market solutions and Sanofi best practicesCoordinate / align with expectations of Product Owner (Werum Pas-X, Opstrakker) to support configuration, implementation, and deployment projectsGuide the team in developing MBRs, Process Instructions, blocks, and templates according to functional specificationsEstablish configuration strategies that leverage market solutions and align with industry best practices and Ensure configurations align with the Core model and operational excellence standardsDelivery and Quality of Services:Drive timely and high-quality delivery of configuration projects while maintaining robust, cost-effective solutionsEstablish and maintain delivery frameworks that ensure consistent, predictable outcomesImplement delivery metrics and KPIs to track performance, quality of service, and team productivityLead risk mitigation strategies to address potential delivery challenges proactivelyCoordinate cross-functional implementation activities to ensure smooth deployment of configurations across different industrial sitesEnsure compliance with legal and regulatory requirements (GxP, Data Privacy, SOX, etc.)Establish delivery governance to maintain transparency and accountability throughout the delivery lifecycleOversee the implementation of various MES projects, including product builds and data foundations, maintaining accountability for the results delivered by MES DevOps Engineers and MBR developersWork closely with product owners and across MES teams to develop and implement strategies supporting product build and configuration, delivery, implementation projectsEnsuring optimal resource allocation and project outcomesOperational Excellence and Continuous Improvement:Drive the implementation of best practices in MES configuration and developmentIdentify opportunities for process optimization and efficiency improvementsLead initiatives to streamline workflows and enhance productivityCollaborate with cross-functional teams to align MES configuration with broader organizational goalsPromote a culture of quality and continuous improvement within the team and across projectsDevelop culture of empowerment, ownership, Thoughtful risk takingStakeholder Management:Collaborate with MES Product Owner, Service manager, capability manager and lifecycle manager and users/ manufacturing sitesWork with Enterprise Architects, solution architects, Quality and the Cybersecurity team to review & qualify configuration designsCommunicate effectively with Digital management teams, staff, and business stakeholdersOversee trainings & knowledge transfer and best practice sharing between the team and sitesEnsure the team provides effective functional & technical support throughout the solution lifecycleBusiness Alignment and Innovation:Analyze business requirements for various processes, providing direction to challenge, consolidate, and develop solutions expandable to multi-business unit use casesDevelop strategies to maximize customer satisfaction while minimizing build and maintenance costs and risksGuide the strategic evaluation of configuration options and assess/manage associated risksRemain current on technology trends and benchmark with other companies to bring innovative inputs to solutionsLead initiatives to evolve GxP Validation approaches to simplify and adapt to next-generation technologiesRequired Skills and Qualifications:Experience & Knowledge:12+ years of work experience in Digital Manufacturing domain, with 8+ years of experience in MES specifically Werum Pas-X Product (Korber) and Opstrakker (elogbook/ eforms)Strong team management experience with demonstrated success in leading and developing technical teamsProven track record of successful delivery of complex technical solutions in regulated environmentsDemonstrated experience in managing delivery timelines, resources, and quality simultaneouslyExperience in multicultural, multilanguage environments and matrixed organizationsBroad knowledge of manufacturing processes in pharmaceutical industrial plantsStrong MES experience: market standards knowledge (solutions, technologies, integration, architecture)Experience & understanding of core product/model conceptTechnical Skills:Expertise in MES solutions: Werum Pas-X (Korber) and Opstrakker (elogbook/ eforms)Strong knowledge of Manufacturing Execution Systems, including Master Batch Record and Review by Exception business processesSolid understanding of manufacturing processes in pharmaceutical plantsStrong knowledge of pharma industry regulatory context (GxP)Knowledge of solution architecture, integration, and infrastructure technologiesKnowledge of Automation layer (SCADA, DCS, PLCs, industrial protocols)Knowledge of scripting (VB etc.) is a plus but not requiredSoft Skills:Strong leadership capabilities with proven ability to inspire and develop teamsHigh degree of accountability and proactive problem-solving mindsetResults-oriented approach with strong focus on delivery excellenceExcellent interpersonal and communication skillsAbility to build and maintain strong relationships across all organizational levelsCustomer-centric approach with focus on delivering valueCollaborative team leader & player with experience in matrix organizationsChange management expertise and ability to adapt to dynamic environmentsStrategic thinking with strong decision-making abilitiesAgile methodology practitionerAbility to manage competing priorities and resilience to deliver under pressureEducation:Engineering degree or Master's in Computer Science or related field (or equivalent experience)MBA or equivalent business management qualification is a plusLanguage:Fluency in English, other languages are a plusWorking Environment:Occasional travel requirement to manufacturing sites in Europe / North America/ AsiaGlobal, matrix organization environmentMust be able to work effectively across different time zones and culturesPursue progress, discover extraordinaryBetter 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 and check out our Diversity Equity and Inclusion actions at !Pursue progress, discover extraordinaryBetter 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 and check out our Diversity Equity and Inclusion actions at !
