Senior Specialist, MES Platform Engineer

Bristol Myers Squibb; Leiden; Hybrid; EUR 90,000 - 120,000; Full time

Job summary

Bristol Myers Squibb in Leiden seeks a Senior Specialist, MES Platform Engineer to administer and enhance Syncade MES within the Digital Plant, collaborating with Manufacturing IT, QA, and CSV to ensure GMP compliance and reliable operations.

You will design Master Recipes, manage master data, user access, reports, and validation activities, driving continuous improvement and MES upgrades to enable efficient manufacturing at the Leiden Cell Therapy Facility.

Qualifications

• Experience with MES systems in GMP environments.
• Strong understanding of MES administration, configuration, and data integrity.

Responsibilities

• Administer and maintain the Syncade MES environment and integrations.
• Design, configure, and maintain Master Recipes and MES objects.
• Manage master data, user access, and reporting/labeling configurations.
• Conduct testing, validation, and compliance activities for GMP/Data Integrity.

Job description

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Position Summary

As part of the Digital Plant department Manufacturing IT Systems & MES for the Leiden Cell Therapy Facility (CTF), the Senior Specialist, MES Platform Engineer is responsible for the administration, maintenance, configuration, and continuous improvement of the Syncade MES (Manufacturing Execution System) environment. 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.

Duties / Responsibilities

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.

#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.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustmentprior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin completing this application, or in any part of the recruitment process, direct your inquiries to [e-mail]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at [e-mail] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1606450 : Senior Specialist, MES Platform Engineer