CAR-T Operations Supervisor at Legend Biotech

As a CAR-T Operations Supervisor, you are the lynchpin of our production. These are your responsibilities:  

✔ Leadership and supervision: You will manage operational teams and supervise various operational units within the CAR-T production process. 

✔ Quality and compliance: You manage all aspects of quality and ensure strict compliance with cGMP standards. As a domain expert for Quality and Operations, you play a central role in GMP inspections. 

✔ Collaboration: You are the first point of contact for production problems and work closely with other departments to find solutions. 

✔ Documentation management: You will manage and review critical documentation within the production areas, such as procedures, work instructions, logs and transfer forms. 

✔ Batch record supervision: You oversee the release and review of batch records for quality control.  

✔ Training: As a manager, you make sure that everyone on your team gets the training they need to perform at their best.  

✔ Operational excellence: You initiate projects that increase efficiency, reduce costs and improve quality. You encourage and inspire your team to continuously improve.   

Education: 

✔ You have a bachelor's or master's degree in science, bioengineering, pharmacy or a related field of study or you are equivalent through experience.  

Experience: 

✔ You have at least 5 years of experience in a cGMP or ATMP environment, preferably in the biotech or pharmaceutical industry. You also have substantial experience with grade C aseptic GMP production.  

Languages: 

✔ You speak and write fluent Dutch and English.  

Strengths: 

✔ You have excellent communication and organizational skills. 

✔ You are an empathetic people manager with strong leadership skills. You have a positive attitude and adapt easily to rapidly changing circumstances. You inspire others to do the same. 

✔ You are good at problem solving, prioritizing and multitasking.  

✔ You have an eye for detail and procedures.   

 Expertise:

✔ You have a thorough knowledge of cGMP regulations and clean room operations. 

✔ You can work fluently with Microsoft Office tools such as Word, Excel, PowerPoint and Outlook.  

✔ Familiarity with Manufacturing Execution Systems (MES) and Electronic Batch Record (EBR) systems is a plus.  

✔ A meaningful job that contributes directly to the well-being of patients.  

✔ An excellent work-life balance. You work 4 days. Then you enjoy 4 days off.  

✔ A supportive and innovative work environment. We value and encourage learning and personal development.  

✔ The opportunity to work with people from all over the world. 

✔ A contract of indefinite duration and an attractive salary package complemented by many fringe benefits, such as additional statutory vacations, meal vouchers, group and hospitalization insurance, double vacation pay, an end-of-year and performance bonus. 

✔ Many fun and informal events. 
 

Legend Biotech is a global biotechnology company dedicated to developing, manufacturing and commercializing innovative and life-saving cell therapies, including treatments for intractable diseases such as cancer.  

Since our founding in 2014 in Somerset, New Jersey, we have grown into a company with more than 2,000 employees in six manufacturing facilities worldwide.  

In Ghent, we are focusing on the production of our advanced CAR-T therapy for the treatment of multiple myeloma, in collaboration with Johnson & Johnson. 

1. You answer a few short questions.
2. You upload your resume or email it later.
3. You will receive a confirmation of your application.
4. Thaella from Legend Biotech will contact you.