We are looking for a driven CAR-T production supervisor for our state-of-the-art manufacturing facility in Ghent. As a CAR-T production Supervisor , you are the lynchpin of our production. 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 c GMP 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.
You will manage and review critical documentation within the production areas, such as procedures, work instructions, logs and transfer forms.
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.
You initiate projects that increase efficiency, reduce costs and improve quality. You encourage and inspire your team to continuously improve.
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 can work fluently with Microsoft Office tools such as Word, Excel, Power Point and Outlook.
Experience with aseptic GMP production is a nice to have
You can work fluently with Microsoft Office tools such as Word, Excel, Power Point and Outlook.
Familiarity with Manufacturing Execution Systems (MES) and Electronic Batch Record (EBR) systems is a plus.
Languages:
~ You speak and write fluent English.
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.
