We are looking for a driven CAR-T production supervisor for our state-of-the-art manufacturing facility in Ghent. Ready for the next step in your career? Then apply today! 

What Can You Expect? 

As a CAR-T production 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.   

Who Are We Looking For? 

Education: 

• You have a bachelor's or master's degree in science, bio-engineering, pharmacy or a related field of study or you are equivalent through experience.  

Experience & Expertise: 

• You have at least 3 years of experience in a GMP or ATMP environment, preferably in the biotech or pharmaceutical industry.
• You have a knowledge of cGMP regulations and clean room operations.
• • You can work fluently with Microsoft Office tools such as Word, Excel, PowerPoint and Outlook.  
• •  
• Experience with aseptic GMP production is a nice to have
• You have a 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.  

Languages:  

• You speak and write fluent 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.

What Do We Offer? 

• 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.  

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