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| Description |
As a Production Supervisor, you are responsible for the daily production process of personalized cell therapy, both for clinical and commercial purposes. You will lead various units within the CAR-T process and ensure safe and compliant production activities in accordance with cGMP requirements — all while coordinating and overseeing operations from your dedicated office workspace, maintaining a clear overview of the production floor and ensuring smooth cross-team collaboration. Tasks: - Lead and supervise operational units within the CAR-T production process, including component preparation, production support, CAR-T processing, filling & finishing, and cryopreservation.
- Act as the primary point of contact for production-related topics, ensuring smooth coordination with Manufacturing Operations, QC IPC, Quality, Facilities & Engineering, MS&T/Manufacturing Excellence, Training, Planning, and Supply Chain.
- Provide hands-on leadership on the shop floor, supporting teams in daily operations, troubleshooting, and decision-making in cGMP environments.
- Serve as a subject matter expert for Quality and Operations and play a key role during GMP inspections and external audits.
- Oversee production quality activities, including documentation management (procedures, work instructions, logs, transfer forms), batch record review and release, and compliance with cGMP standards.
- Coordinate quality system processes such as Change Controls, Deviations/Events, and CAPA.
- Guide and support team development through structured training and operational coaching.
- Drive operational excellence by leading process improvements focused on efficiency, cost reduction, and quality enhancement.
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| Company |
Our client, Legend Biotech, based in Zwijnaarde, is a global biotechnology company bringing the innovative CAR-T cell therapy to Ghent. With this, the Legend Biotech team makes a daily difference in the lives of many patients suffering from cancer and other life-threatening diseases.
They are currently in a phase of strong growth and are looking for motivated and dedicated team members
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| Profile |
Who we are looking for: - Bachelor’s or Master’s degree in Science, Bio-Engineering, Pharmacy, or a related field, or equivalent through experience.
- Minimum 3 years of experience in a production environment, preferably in biotech or biopharma.
- Strong experience in management, for example as a production lead, supervisor, or similar leadership role.
- Solid knowledge of cGMP regulations, cleanroom operations, and familiarity with Microsoft Office; experience with MES/EBR systems is a plus.
- Strong communication, organizational, and leadership skills with an empathetic and people-oriented management style.
- Positive, flexible, and capable of prioritizing, multitasking, and solving problems effectively, with a strong attention to detail.
- Fluent in English (additional languages are a plus).
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| Offer |
What we offer you: - A meaningful job that directly contributes to the well-being of patients.
- Work in a supportive, innovative, and diverse team, where learning, personal development, and loyalty are encouraged.
- Collaborate with colleagues from around the world in an environment that values team spirit.
- Celebrate legendary moments with treats, fun gadgets, and enjoyable events.
- Attractive salary package including shift premiums, meal vouchers, group and hospitalization insurance, double vacation pay, and end-of-year and performance bonuses.
- A meaningful job with an excellent work-life balance. You will work 4 days. After that you will enjoy 4 days off. This position operates within our future (rotating) night shift system. Please be prepared to work across various shifts starting from 6AM and ending by 2AM as well as our night shifts ranging from 6PM until 4 AM and 8 PM until 6AM. While night shifts are not currently in place, employees hired for this role should be willing and able to work within the (rotating) night shift system once implemented.
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