Bristol Myers Squibb
Senior Specialist, MES Platform Engineer
Leiden – NL, NL · Senior
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About the role
- The role combines technical system administration responsibilities with recipe authoring expertise to ensure reliable MES operations, GMP compliance, optimal system performance, and efficient execution of manufacturing processes.
- The position serves as a key bridge between manufacturing operations, quality, validation, and IT teams by supporting MES infrastructure, user administration, master data management, recipe development, system enhancements, and business process improvements.
- Monitor MES application health, availability, performance, and underlying hardware components.
Responsibilities
- Manage and maintain the MES application environment, including integrations and peripheral devices such as scanners and label printers.
- Support installation, configuration, upgrades, patches, and lifecycle management activities.
- Perform routine system reviews and execute corrective and preventive measures to maintain system reliability.
- Collaborate with Shared Services and infrastructure teams to define and manage application versus infrastructure responsibilities.
- Recipe Design & Configuration
- Design, configure, document, and maintain Master Recipes using standardized corporate objects and approved building blocks.
- Maintain and enhance existing recipes while ensuring consistency, usability, and compliance.
- Evaluate and implement new objects, templates, and configuration components supporting recipe development and manufacturing improvements.
- Manage MES user access in compliance with approved procedures and regulatory requirements.
- Support periodic access reviews and maintain appropriate segregation of duties.
Requirements
- Required Knowledge & Experience
- Strong understanding of Manufacturing Execution Systems (MES) and manufacturing processes.
- Experience with MES recipe authoring, configuration management, and system administration.
- Knowledge of GMP, GxP, Data Integrity, and Computer System Validation practices.
- Experience managing master data, user access, and system configuration.
- Proficiency in troubleshooting, root cause analysis, system monitoring, and performance optimization.
- Experience supporting MES upgrades, change management, and validation activities.
- Ability to work effectively in a highly regulated biopharmaceutical manufacturing environment.
- If this posting is missing required information required by local law or incorrect, contact BMS at TAEnablement@bms.com with the Job Title and Requisition number.
Skills
- Emerson Syncade MES
- MES Reporting
- Label and Form Design
- Change Control & Validation Processes
- Incident & Problem Management
- Data Integrity Principles
- #LI-Hybrid
- How We Work
- Supporting People with Disabilities
- Candidate Rights
- BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
- ISA-95
Company info
- If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com.
This listing is sourced directly from Bristol Myers Squibb's careers page and normalized into a canonical job model.