
MES DevOps Engineer - Siemens OPCenter
Hyderabad, Indien Permanent Gepostet am Jul. 24, 2025 Endet am Jul. 30, 2025About the job
Company Context
Sanofi'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 process
Deliver innovative "state of the art" tools enabling performance for manufacturing processes
Allow new generation of deployment – more Agile & business centric
Maintain robust and highly available solutions to operate industrial processes efficiently
Role Overview
The Manufacturing Execution System (MES) DevOps Engineer drive the design, build, and lifecycle of global end-to-end MES solutions. You will ensure local configurations align with the Core model and operational excellence standards while guaranteeing and promoting the right usage of Sanofi Digital and Industrial standards for Processes, Applications, and Infrastructure environments.
You will leverage the Digital Portfolio's Detail Design documents, catalogue of services, and existing Core building blocks while supporting sites in troubleshooting and remediation action plans. Working in close collaboration with MES Product Owners, MES DevOps Manager, MBR Developer, MES Full Stack Engineers, MES installers/developers, Product lines, local digital teams, Business Process Owners, Archetype leads, Site modelers, and Shopfloor experts, you will remain current on company standards, Digital industry practices, and emerging standards while contributing to Digital standards maintenance.
Systems & Processes in Scope
Main MES Systems:
Siemens MES Opcenter Execution Pharma Product
Siemens Equipment logbook Pharma
Main platform :
Mendix
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
Instructions for Operating Text
Production execution
Weighing & Dispensing
Communication to equipment or SCADA systems
Equipment management
Material flow management
Traceability / Genealogy
Labelling
Reporting
Interface with ERP, quality, logistics & shopfloor systems (LIMS, Documentation, Deviation management, Serialization, eOEE)
Main Responsibilities:
Key Responsibilities
Understand business requirements (including analytics) for various processes, challenge, consolidate, and extrapolate them to design & build solutions expandable to multi-business unit use cases and plant configurations
Maximize customer satisfaction while minimizing build and maintenance costs and risks associated with fulfillment of business needs
Implement appropriate services to ensure optimal allocation of all available capabilities
Evaluate impact analysis of solution options and assess/manage associated risks
Conduct end-to-end business process analysis including integration with partner systems (ERP, shopfloor systems, automation layers), labelling technologies, and mobile technologies
Stakeholder Management & Training
Coordinate, inform, and ensure functional expertise in a matrix context
Transfer know-how, experience, and best practices to sites
Contribute to Digital skills development within your domain
Provide functional & technical support during the full solution lifecycle and to the sites
Ensure adoption and adequate use of solutions
Deliver on-site training to manufacturing sites
Delivery & Quality of Services
Design and build MBRs, Process Instructions, blocks, and templates including Functional specifications
Configure & implement core solutions as close to standard market solutions as possible, based on state-of-the-art best practices
Aim to align processes and enable industrial efficiency across different Sanofi industrial sites
Define appropriate design & build of solutions by adopting GxP validations
Participate in regular design reviews with site modelers to ensure best practices are followed
Perform or participate in regular MBR reviews for sites
Ensure technical solutions comply with recommendations for Quality, Security, and Accessibility
Lead the on-time delivery of projects while ensuring robust, cost-effective solutions
Safeguard proper deployment of core solutions on different industrial sites
Participate in defining indicators for performance and quality of service, monitor and communicate them
Manage preventive/corrective maintenance for components
Ensure standards and rules for Platform Management (Release management, Solution Documentation, Testing) are correctly understood and applied
Manage incidents & corrective/preventive actions
Strategy Development & Implementation
Remain current on technology trends and benchmark with other companies and partners to bring innovative inputs to solutions, operating models, and strategy
Collaborate with peers (Enterprise Architects, solution/ technical architects, Quality, Cybersecurity) to review and qualify solution design and/or introduction of new technology
Explain/present architecture and technical matters in an understandable way to Digital management team, staff, and business stakeholders
Break current GxP Validation established postulates to simplify and adapt to current and next-generation technologies & methodologies (Cloud, Service Management, Agile)
About You
Experience & Knowledge
8+ years of work experience in Digital for Manufacturing domain, with 5+ years of experience in MES, specifically Siemens OPCenter Execution Pharma and Siemens Equipment logbook
Demonstrated experience in multicultural/multilanguage environments and matrixed organizations
Broad knowledge of manufacturing processes in industrial plants
Strong MES experience: market standards knowledge (solutions, technologies, integration, architecture), process industry within life science/pharmaceutical industries
Experience & understanding of core product/model concept
Successful and significant Project Management experience is a plus
Technical Skills
Expertise in MES solutions: Siemens OPCenter Execution Pharma and Siemens Equipment logbook
Strong knowledge of Manufacturing Execution Systems, including Master Batch Record and Review by Exception business processes
Solid understanding of manufacturing processes in pharmaceutical plants
Strong knowledge of pharma industry regulatory context (GxP)
Strong knowledge of Digital technologies & concepts
Knowledge of Automation layer (SCADA, DCS, PLCs, industrial protocols)
Good experience & knowledge of Mendix
Knowledge of Scripting (VB/.Net) development & validation
JSON development is a plus
Knowledge of reporting tools (Power BI) is a plus
Soft Skills
Accountability and reliability
Customer-driven mindset
Fast learner, proactive, willing to apply change management
Ability to deal with ambiguous situations
Strong focus on value delivery, with ability to work autonomously on solution design
Ownership and leadership within assigned scope
Agile methodology practitioner
Communication and interaction skills
Ability to challenge, open-minded and active listening
Ability to explain complex matters in a simple and understandable way
Education
Engineering degree or Master's in Computer Science or related field (or equivalent experience)
Language
Fluent in English, other languages are a plus
Working Environment
Travel requirement: 30% of time to manufacturing sites in Europe, North America & Asia
Global, matrix organization environment
Must 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!
Strebe nach Fortschritt. Entdecke Einzigartiges.
Werde Teil von Sanofi und starte mit uns in eine neue Ära der Wissenschaft – wo dein persönliches Wachstum genauso wegweisend ist wie unsere Arbeit. Wir investieren in dich, damit du weiterkommst, schneller denkst und Dinge möglich machst, die vorher undenkbar waren. Du wirst Grenzen verschieben, Gewohntes hinterfragen und smarte Lösungen entwickeln, die direkt bei den Menschen ankommen, für die wir da sind. Bereit, die Wunder der Wissenschaft zu jagen und Leben zu verbessern? Dann lass uns gemeinsam Großes bewegen – und das Außergewöhnliche entdecken.
Bei Sanofi stehen allen die gleichen Chancen offen – unabhängig von Herkunft, Hautfarbe, Religion, Geschlecht, Nationalität, sexueller Orientierung, Alter, Staatsangehörigkeit, Familienstand, Behinderung, Geschlechtsidentität, Veteranenstatus oder anderen gesetzlich geschützten Merkmalen.
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