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CAR-T production supervisor
Ver: 105
Dia de atualização: 06-12-2025
Localização: Ghent East Flanders
Categoria: Gestão executiva Produção / Operação
Indústria: Biotechnology Research
Posição: Mid-Senior level
Tipo de empregos: Full-time
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Conteúdo do emprego
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.
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.
- 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.
- You speak and write fluent English.
- 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.
- 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 maintains a drug-free workplace.
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Data limite: 20-01-2026
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