MES Specialist

Sanofi

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
Swiftwater, PA
Posted
14 days ago
Freshness
Confirmed live yesterday
Closes
Oct 20, 2026
Nearby
8 roles within 25 mi

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Salary context

How this pay compares to similar roles

Similar $151k
$121k most similar roles pay here $182k

This listing doesn't post a salary. Most similar roles pay $127,250–$174,600.

Based on 240 similar postings.

Employer

About Sanofi

Sanofi is a French global R&D-driven and AI-powered biopharmaceutical company focused on human health through specialized medicine, vaccines, and consumer healthcare.

Sanofi currently has 4 open roles on FindRole.

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At a glance

TL;DR · MES Specialist

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The MES Specialist joins the Manufacturing Systems & Automation department to provide daily support for the site manufacturing execution system and automation. This role involves managing electronic batch record (EBR) configurations, supporting new product and process deployments, and performing troubleshooting as part of an on-call rotation. Key responsibilities include developing MES solutions, ensuring seamless integration with digital applications, maintaining GMP compliance through rigorous validation protocols, and coordinating with vendors for manufacturing systems. The candidate will also create training materials for operations staff and lead cross-functional teams through design reviews. Required technical expertise includes Siemens OpCenter, DeltaV DCS, Aveva SCADA, PLCs, and OPC data integration for Historian or ERP connectivity. This role addresses the critical challenge of ensuring reliable production, quality control, and data management within a biopharma manufacturing environment to support large-scale healthcare solutions.

Skills

Siemens OpCenter EBR DeltaV Aveva SCADA DCS OPC Historian ERP GMP System Validation Data Integration

What you'll do

  • Develop MES/EBR solutions including recipe configurations and system changes to meet business requirements.
  • Manage the configuration, implementation, and troubleshooting of electronic batch records (EBR) within the site MES.
  • Ensure all systems comply with GMP and regulatory standards through detailed documentation and validation testing.
  • Integrate manufacturing systems with digital applications for production, quality control, and data management.
  • Develop and deliver specialized training materials and sessions for operations staff on system usage.
  • Provide technical application support and participate in a rotating on-call schedule for manufacturing operations.
  • Coordinate with cross-functional teams to gather requirements and lead design reviews or user acceptance testing.

What we're looking for

  • Bachelor's degree in engineering, computer science, biotechnology, or a related field in the biopharma sector.
  • At least 1 year of experience in MES/eBR and automation support within biopharma or related industries.
  • Hands-on experience with Siemens OpCenter MES platform configuration.
  • Expertise with DCS (DeltaV), SCADA (Aveva), PLCs, and other manufacturing automation technologies.
  • Experience with machine connectivity and data acquisition from PLCs into Historians or ERPs using OPC.
  • Ability to develop and implement electronic batch record (EBR) solutions and configurations.
  • Knowledge of GMP and regulatory standards for system validation and documentation.
  • Strong communication skills for cross-functional team collaboration and stakeholder interaction.

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