Full-Time
MES Configuration Expert
PAS-X
Updated on 9/3/2026
Sanofi
10,001+ employees
Global pharma company; vaccines and R&D
Compensation Overview
€49.6k - €74.4k/yr
Barcelona, Spain
Hybrid
Hybrid work arrangement indicated.
Master's
 IT Operations (1) |
|---|
Get referred to Sanofi
See people who can refer or advise you
- At least 5 years of work experience in the Digital for Manufacturing domain, ideally with Manufacturing Execution Systems, specifically Werum PAS-X and Opstrakker.
- Experience working in multicultural, multilingual environments and matrixed organizations.
- Broad knowledge of manufacturing processes in industrial plants.
- Strong Manufacturing Execution Systems experience, including market standards, solutions, technologies, integration, and architecture in life-science or pharmaceutical process industries.
- Experience and understanding of core product and model concepts.
- Expertise in Werum PAS-X (Körber) and Opstrakker (elogbook/eforms).
- 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 the pharmaceutical industry's GxP regulatory context.
- Strong knowledge of digital technologies and concepts.
- Knowledge of the automation layer, including SCADA, DCS, PLCs, and industrial protocols.
- Knowledge of scripting development and validation using VB/.NET.
- An engineering degree or a Master's in Computer Science or a related field, or equivalent experience.
- Mandatory English language proficiency.
- Guarantee and promote the correct use of Sanofi Digital and Industrial standards for processes, applications, and infrastructure environments.
- Leverage Detail Design documents, the catalogue of services, and existing Core building blocks.
- Support sites with troubleshooting and remediation action plans.
- Work with MES Product Owners, MES Configuration Experts and Leads, MBR Developers, MES installers and developers, product lines, local digital teams, Business Process Owners, Archetype Leads, Site Modelers, and Shopfloor Experts.
- Remain current on company standards, digital industry practices, and emerging standards, and contribute to maintaining digital standards.
- Understand business requirements, including analytics, and challenge, consolidate, and extrapolate them to design and build solutions that support multiple business units and plant configurations.
- Maximize customer satisfaction while minimizing build and maintenance costs and risks associated with fulfilling business needs.
- Implement appropriate services to optimize allocation of available capabilities.
- Evaluate solution options through impact analysis and assess and manage associated risks.
- Conduct end-to-end business process analysis, including integration with partner systems, labeling technologies, and mobile technologies.
- Provide functional and technical support throughout the solution lifecycle and to sites.
- Participate in regular design reviews with Site Modelers to ensure best practices are followed.
- Perform or participate in regular Master Batch Record reviews for sites.
- Manage incidents and corrective/preventive actions.
- Manage preventive and corrective maintenance for components.
- Ensure technical solutions comply with Quality, Security, and Accessibility recommendations.
- Design and build Master Batch Records, Process Instructions, blocks, and templates, including Functional Specifications.
- Configure and implement Core solutions as close to standard market solutions as possible, based on current best practices.
- Align processes and enable industrial efficiency across different Sanofi industrial sites.
- Define appropriate solution design and build using GxP validations.
- Lead on-time project delivery while ensuring robust, cost-effective solutions.
- Safeguard proper deployment of Core solutions across industrial sites.
- Participate in defining performance and quality-of-service indicators, monitor them, and communicate them.
- Ensure Platform Management standards and rules for release management, solution documentation, and testing are understood and applied.
- 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 the domain.
- Ensure adoption and appropriate use of solutions.
- Deliver on-site training to manufacturing sites.
- Remain current on technology trends and benchmark with other companies and partners to provide innovative input to solutions, operating models, and strategy.
- Collaborate with Enterprise Architects, solution and technical architects, Quality, and Cybersecurity to review and qualify solution designs and new technology introductions.
- Explain and present architecture and technical matters clearly to digital management, staff, and business stakeholders.
- Simplify and adapt established GxP validation approaches to current and next-generation technologies and methodologies, including cloud, service management, and Agile.
- Successful and significant Project Management experience.
- Knowledge of Siemens Opcenter Execution Pharma.
- JSON development.
- Knowledge of reporting tools such as Power BI.
- Low-code application development using Mendix.
- AI-assisted MES solution development using GitHub Copilot, Claude, or Microsoft Copilot.
- Knowledge of cloud architecture and services, preferably Azure.
- Other language proficiency.
Sanofi is a global pharmaceutical and biotechnology company that develops, manufactures, and sells prescription medicines, over-the-counter products, and vaccines. Its products span immunology, oncology, rare diseases, and vaccines, addressing unmet medical needs through a strong focus on research and development. Sanofi's core product model relies on large-scale R&D, strategic partnerships, and licensing to bring new therapies to markets, with revenue generated from product sales and collaborations. The company differentiates itself by leveraging its global reach, diverse portfolio, and emphasis on patient-centric solutions, safety, and quality to navigate regulatory environments in developed and emerging markets. The company’s goal is to improve health outcomes and quality of life for people worldwide by delivering innovative treatments and vaccines that meet unmet medical needs.
Company Size
10,001+
Company Stage
IPO
Headquarters
Paris, France
Founded
1973
Get referred to Sanofi
See people who can refer or advise you
Simplify's Take
What believers are saying
- Q2 2026 sales rose 17.8% at constant exchange rates, and guidance increased.
- Pharma launches grew 48.3% in Q2 2026, led by Ayvakit, ALTUVIIIO, Sarclisa.
- R&D leadership reset under Paulo Fontoura targets faster pipeline conversion from September 2026.
What critics are saying
- BluePrint layoffs of 229 staff run through June 2027, signaling integration strain.
- FDA rejected Cenrifki in December 2025; U.S. multiple sclerosis sales stay blocked.
- Vaccines sales fell 4.7% in Q2 2026, exposing dependence on Dupixent and launches.
What makes Sanofi unique
- Dupixent topped €5.2 billion in Q2 2026, proving immunology dominance.
- Sanofi delivered seven Q2 2026 regulatory approvals across immunology, rare disease, oncology, neurology.
- Cenrifki and Sarclisa Escena show a pipeline converting science into differentiated launches.
Help us improve and share your feedback! Did you find this helpful?
Benefits
Health Insurance
Professional Development Budget
Parental Leave
Company News
Atlanta-based Altesa BioSciences has won the 2026 Georgia Life Sciences Golden Helix Award for Deal of the Year, recognising its oversubscribed $75 million Series B financing round. The funding, led by Forbion with participation from Sanofi, Medicxi, Pitango, and Atlantic Partners, will advance the clinical-stage pharmaceutical company's lead therapy, vapendavir. Vapendavir is an investigational oral treatment for chronic lung diseases including COPD and asthma. The drug is currently being evaluated in the Phase 2b CARDINAL trial, which will enrol 900 COPD patients across the US and UK. The Georgia Research Alliance Venture Fund was an early investor in Altesa. The company's scientific founders previously helped develop molnupiravir, one of the earliest COVID-19 treatments.
Epicrispr Biotechnologies Closes $90 Million Series C Financing to Advance First-in-Class Epigenetic Therapy Toward Pivotal Studies in FSHD
InduPro has closed a $77 million Series B financing round and dosed its first patient in a Phase 1 study of IDP-001, its lead oncology programme. The biotechnology company is developing IDP-001, a bispecific antibody-drug conjugate targeting EGFR and a novel tumour-associated proximity antigen, for treating advanced squamous non-small cell lung cancer and other solid tumours. The Column Group led the financing round, with participation from Vida Ventures, MRL Ventures Fund, Emerson Collective, Euclidean Capital, Solasta Ventures, Sanofi, and Eli Lilly and Company. Proceeds will support Phase 1 clinical development and early proof-of-concept data generation for IDP-001, whilst advancing InduPro's broader preclinical pipeline. InduPro uses a proximity-guided platform to map protein spatial relationships on cell surfaces for discovering selective co-target pairs.
Scribe Therapeutics, a clinical-stage biotechnology company developing in vivo CRISPR technologies, has priced its upsized initial public offering at $15.00 per share, the high end of its range. The company is offering 8,580,000 shares, expecting to raise $128.7 million in gross proceeds before fees and expenses. Scribe has also granted underwriters a 30-day option to purchase up to 1,287,000 additional shares. The shares are expected to begin trading on the Nasdaq Global Market on 24 July 2026 under the ticker symbol "SCTX", with the offering closing on 27 July 2026. Additionally, Scribe has agreed to sell 500,000 shares at the same price to Sanofi in a concurrent private placement. Leerink Partners, Goldman Sachs, Guggenheim Securities, and Wells Fargo Securities are serving as joint book-running managers.
The US Food and Drug Administration has approved Sanofi's subcutaneous Sarclisa Escena for treating multiple myeloma, making it the first anticancer treatment administered through an on-body injector. The therapy uses Enable Injections' CirCLIQ device, which delivers the drug automatically with a retractable 30g needle. The approval was supported by the IRAKLIA phase 3 study, which demonstrated that Sarclisa Escena delivered via the on-body injector provided similar efficacy and safety compared to intravenous infusion, with significantly shorter treatment time and fewer infusion-related reactions. The study showed a 71.1% objective response rate in patients with relapsed or refractory multiple myeloma. More than 70,000 patients worldwide have been treated with Sarclisa-based regimens. The on-body injector aims to reduce physical burden on healthcare providers whilst offering patients greater convenience during treatment.