MES Engineer

Johnson & Johnson Co.; Gent; On-site; EUR 60,000 - 96,000; Full time

Job summary

Johnson & Johnson is seeking a MES Engineer – PAS-X in Ghent to design, configure, and maintain MES solutions supporting CARVYKTI manufacturing. You will develop eBRs, master data, and ensure compliance with GMP and site standards in a fast-paced environment.

The role emphasizes validation, cross-functional collaboration, and continuous improvement, with opportunities to contribute to digital manufacturing and lifecycle management within the CAR-T network.

Qualifications

• Master's degree required; 2–5 years in regulated manufacturing or MES environments desired.
• Experience with MES, validation lifecycle, and system deployments is essential.

Responsibilities

• Design, configure, and maintain PAS-X MES solutions to support CARVYKTI manufacturing.
• Translate requirements into MES designs and system configurations.
• Develop and maintain electronic batch records (eBRs) and master data.
• Ensure MES aligns with GMP, site standards, and data integrity.
• Coordinate validation activities and testing with stakeholders.
• Support continuous improvement and cross-functional collaboration.

Skills

MES experience

PAS-X

GMP knowledge

Validation

Analytical skills

Stakeholder management

English fluent

Education

Master's degree in Engineering, Computer Science, Life Sciences, Biotechnology, Pharmaceutical Sciences, or related field

Tools

Werum PAS-X

eBR

Job description

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

Process Engineering

Job Category

Scientific/Technology

All Job Posting Locations

Gent, East Flanders, Belgium

Job Description

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

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.

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 through MES enhancements.
• Support project execution and change implementation activities from requirements gathering through deployment.
• Foster a culture of innovation, continuous improvement, and operational excellence within the CAR‑T manufacturing environment.

6. Strategic Contribution

• Contribute to the evolution of the MES roadmap supporting CARVYKTI manufacturing in Ghent.
• Support digital transformation initiatives aimed at improving process robustness, data visibility, and manufacturing efficiency.
• Act as a key advocate for MES best practices and digital manufacturing excellence across the CAR‑T network.

QUALIFICATIONS

Education

• A Master's degree in Engineering, Computer Science, Life Sciences, Biotechnology, Pharmaceutical Sciences, or a related field is required.

• 2-5 years of experience in manufacturing, automation, MES, digital systems, validation, or manufacturing support functions within regulated environments.
• Hands‑on experience with Manufacturing Execution Systems (MES), preferably Werum PAS‑X, including configuration, eBR development, or MES deployments.
• Knowledge of GMP/GxP‑regulated pharmaceutical, biotechnology, cell therapy, biologics, or advanced therapy manufacturing environments and associated manufacturing processes.
• Strong understanding of system design, electronic batch records (eBR), master data management, computerized system validation (CSV), qualification, and validation lifecycle activities.
• Experience supporting system integrations with ERP, LIMS, automation platforms, and other manufacturing systems, along with change control, deviation management, and CAPA processes.
• Excellent analytical, troubleshooting, and problem‑solving skills, with the ability to manage multiple priorities, work independently, and maintain a strong focus on quality and data integrity.
• Strong communication and stakeholder management skills, with a proactive, continuous improvement mindset; fluency in English is required and Dutch is an advantage.

There is a pre‑identified candidate for this position

At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.

Finally, at the end of the process, we’ll invite you to share feedback in a short survey — your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We’re excited to learn more about you and wish you the best of luck in the process!

Required Skills

Preferred Skills

Analytical Reasoning, Computerized Equipment Skills, Emerging Technologies, Gemba Kaizen, Issue Escalation, Lean Supply Chain Management, Problem Solving, Process Control, Process Engineering, Process Oriented, Product Improvements, Science, Technology, Engineering, and Math (STEM) Application, Situational Awareness, Supply Planning, Technical Research, Technologically Savvy, Validation Testing

The anticipated base pay range for this position is

€60.000,00 - €96.255,00

Benefits

In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well‑being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well‑being & career growth | Johnson & Johnson Careers.

*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.