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Johnson & Johnson (J&J) is recruiting a QA Project Manager for the CAR-T hub in Europe. The position will be based in Ghent Belgium.

CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system. They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.

To support the CAR-T program in EMEA, J&J has constructed two CAR-T manufacturing centers in the Ghent area (Belgium). The QC laboratories will be operated from the existing J&J Beerse site. CAR-T investigational medicinal and commercial CAR-T products are manufactured in the Ghent facilities.

The successful candidate will be responsible for ensuring that the manufacturing processes meet quality standards and regulatory requirements. This role involves working closely with cross-functional teams, including Technical Operations, Manufacturing, Vein-to-Vein department and Regulatory Affairs, to drive continuous improvement and support the development and commercialization of CAR T-cell therapies.

The QA Project Manager, CAR-T Europe is responsible to ensure Lead and manage the quality assurance activities for CAR T cell therapy projects, ensuring compliance with regulatory standard.

Major Responsibilities:

• Quality Assurance Oversight: Monitor and ensure adherence to Good Manufacturing Practices (GMP/ATMP) and other relevant quality standards during the manufacturing of CAR T-cell products.


• Project Management: Lead and manage the quality assurance activities for CAR T cell therapy projects, ensuring compliance with regulatory standards. Develop, implement, and maintain QA strategies, policies, and procedures specific to CAR T manufacturing. Collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to establish quality requirements and acceptance criteria.


• Risk Management: Conduct risk assessments for CAR T projects, identify potential quality issues, and develop mitigation strategies to address identified risks.


• Document Control: Review and approve project-specific documents, including protocols, standard operating procedures (SOPs), batch records, and validation reports.


• Deviation & CAPA Management: Investigate deviations, non-conformances, and implement corrective and preventive actions (CAPAs) to ensure process integrity and product quality.


• Change Control: Evaluate and implement changes related to CAR T-cell processes, equipment, and materials, ensuring all changes comply with quality standards and regulatory requirements.


• Audits & Inspections: Prepare for and participate in internal and external audits and inspections. Lead audit response activities and implement corrective actions as necessary.


• Collaboration: Collaborate with internal teams and external partners to support the project from development to manufacturing, ensuring quality requirements are met at all stages.


• Continuous Improvement: Establish and maintain effective working relationships with the different business partners and Legend Biotech to ensure alignment of objectives and deliverables.