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 https: //www.jnj.com

Job Function:

Job Sub Function:

Job Category:

All Job Posting Locations:

Job Description:

This position will be part of the CAR-T Asset Engineering team within the Make Asset Management organization (MAM). The Asset Engineer is responsible for providing technical expertise on the lab equipment (asset) of the CAR-T process as well as performing Commissioning and Qualification activities within the cGMP Clinical and Commercial Cell Therapy Manufacturing plants serving Ghent and Beerse sites. The role will be a key contributor to ensure flawless operation and asset management projects in close collaboration with the different project organizations, vendors, sites, and stakeholders.

Imagine empowering the body’s own immune system to fight cancer. That’s exactly what CAR-T therapy does. It uses a patient’s own T-cells, reprogramming them to target and destroy cancer cells. This advanced therapy holds the promise to change lives — and you can be part of that journey !

Key Responsibilities:

• Manages multiple business requests and/or small projects equipment related
• Supports in planning and execution of C& Q activities
• Provide SME knowledge and support for troubleshooting scenarios
• Sustains continuous technical improvements around our Asset base
• Drive to solutions by coordinating with other internal departments and/or outside suppliers
• Supports technical investigations detected during C& Q activities.

Qualifications

Education:

• A minimum of a Master’s Degree in Science, Engineering, Bioengineering or equivalent technical discipline is required.

What You Bring

• 4+ years of experience in the pharmaceutical manufacturing / engineering environment
• Experience in commissioning & qualification (C& Q) is a Plus.
• A hands-on, solution-oriented mindset.
• A strong understanding of GMP guidelines and experience with audits or inspections.
• A collaborative and open approach — you thrive on teamwork and knowledge sharing.
• Demonstrate ownership and strong analytical/communication skills
• Fluent in English (written and spoken), Dutch language is a Plus

What We Offer

• A meaningful role where your work has a direct impact on cancer patients’ lives.
• A supportive environment that values your growth, creativity, and contributions.
• A diverse and inclusive workplace where everyone can thrive.