Senior Specialist, MES Platform Engineer
About the role
Position Summary
MES System Administration & Maintenance
- Manage and maintain the MES application environment, including integrations and peripheral devices such as scanners and label printers.
- Monitor MES application health, availability, performance, and underlying hardware components.
- 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.
- Analyse business requirements and translate operational processes into MES solutions.
- 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.
Master Data & User Administration
- Execute master data management activities to ensure data integrity and consistency within MES.
- Manage MES user access in compliance with approved procedures and regulatory requirements.
- Support periodic access reviews and maintain appropriate segregation of duties.
- Configure and maintain MES system settings supporting manufacturing operations.
Reporting, Labels & Configuration Management
- Create and maintain MES reports, labels, label formats, and related configuration designs.
- Support manufacturing operations through effective reporting and labelling solutions.
- Maintain documentation and traceability related to MES configuration changes.
Testing, Validation & Compliance
- Develop and execute testing activities supporting new recipes, system changes, and MES enhancements.
- Support creation of User Acceptance Test (UAT) scripts and validation deliverables.
- Participate in dry runs, qualification activities, and validation reviews.
- Ensure MES solutions remain compliant with GMP, GxP, Data Integrity, and Computer System Validation requirements.
- Support risk assessments, impact assessments, and change control activities.
System Upgrades & Continuous Improvement
- Support MES upgrade projects, platform enhancements, and technology lifecycle initiatives.
- Identify opportunities to optimize MES processes, improve user experience, and increase manufacturing efficiency.
- Partner with local and global MES teams to implement best practices and standardized solutions.
- Contribute to the long-term MES roadmap and system sustainability initiatives.
Incident & Operational Support
- Provide second-line support for MES incidents, service requests, and operational issues.
- Troubleshoot application, configuration, recipe, integration, and performance issues.
- Restore MES availability in alignment with business continuity requirements, urgency, and severity classifications.
- Participate in investigations and implementation of corrective actions related to MES events and deviations.
Collaboration & Leadership Support
- Work closely with Manufacturing, QA, MSAT, CSV, and IT stakeholders to ensure MES solutions meet business needs.
- Collaborate with peer MES administrators and recipe authors across CTF sites.
- Assist the Senior Manager Manufacturing IT Systems & MES in responsibilities associated with Technical System Ownership, Configuration Item Ownership, governance, and continuous improvement initiatives when required.
Reporting Relationship
Collaborates With
- MES Recipe Authors
- Manufacturing Support IT
- IT Automation
- Shared Services IT
- Quality Assurance (QA)
- Manufacturing Science & Technology (MSAT)
- Computer System Validation (CSV)
- Manufacturing Operations
- Global MES Teams
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.
- Strong problem-solving, communication, and stakeholder management skills.
- Ability to work effectively in a highly regulated biopharmaceutical manufacturing environment.
Technical Skills
- Emerson Syncade MES
- SQL
- ISA-95
- MES Reporting
- Label and Form Design
- Change Control & Validation Processes
- Incident & Problem Management
- Data Integrity Principles
#LI-Hybrid
We hire for skills and capabilities, not just credentials - if this role excites you, but doesn't perfectly match your resume, we encourage you to apply anyway.
How We Work
Where you work matters - because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.
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