MES Engineer CAR-T
Johnson & Johnson
- Location
- Gent, East Flanders, Belgium
- Work model
- On-Site
- Level
- Mid
- H-1B history
- 2 approvals (FY2023)
- Posted
- Aug 24, 2026
About this role
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Supply Chain Engineering Job Sub Function: Manufacturing Engineering Job Category: Scientific/Technology All Job Posting Locations: Gent, East Flanders, Belgium Job Description:
JOB SUMMARY
CAR-T is an innovative treatment that harnesses the power of a patient's own immune system. By genetically modifying a patient's T-cells to target and destroy cancer cells, this breakthrough technology offers new hope to patients for whom conventional therapies no longer provide adequate results. Join our innovative team within the Manufacturing Asset Management (MAM) organization in Ghent as a MES Engineer supporting the PAS-X Manufacturing Execution System (MES) for CARVYKTI manufacturing. In this role, you will play a key part in designing, maintaining, qualifying, and continuously improving MES solutions that support GMP manufacturing operations and ensure the reliable execution of critical production processes. This is a unique opportunity to develop expertise at the intersection of cell therapy manufacturing, digital systems, and operational excellence while contributing directly to the delivery of life-changing treatments to patients worldwide. As a MES Engineer – PAS-X, your main responsibilities include: 1. MES Design & Configuration Design, configure, and maintain PAS-X MES solutions to support manufacturing processes across the CARVYKTI production lifecycle. Translate business and operational requirements into compliant MES designs and system enhancements. Develop and maintain electronic batch records (eBRs), workflows, master data, and system configurations. Ensure MES solutions remain aligned with evolving business needs, GMP requirements, and site standards. 2. Qualification & Validation Support Support qualification and validation activities for MES deployments, enhancements, and periodic updates. Author and review validation documentation, including requirements, risk assessments, test protocols, and summary reports. Coordinate testing activities with Operations, Quality, Validation, and IT stakeholders. Ensure all MES changes are implemented in accordance with applicable quality and compliance requirements. 3. System Support & Issue Resolution Serve as a technical MES subject matter expert and support manufacturing operations in the resolution of system-related issues. Investigate and troubleshoot MES incidents, deviations, and system events to minimize operational impact. Contribute to knowledge management, user training, and support documentation to strengthen operational readiness. 4. Master Data & Lifecycle Management Maintain oversight of MES master data, ensuring accuracy, consistency, and compliance throughout the system lifecycle. Support controlled deployment of process updates, recipes, materials, equipment models, and workflow modifications. Ensure data integrity and traceability across MES processes and integrations. Participate in system lifecycle activities, including upgrades, patching, and platform improvements. 5. Continuous Improvement & Cross-Functional Collaboration Identify opportunities to improve manufacturing efficiency, compliance, and user experience