CAR-T Production Supervisor
Manufacturing I GMP I Leadership I operations I Production I English I Ghent | 1108337
Your new company
Legend Biotech is a global biotechnology company dedicated to developing, manufacturing, and commercializing innovative and life-saving cell therapies for the treatment of chronic and life-threatening diseases, such as cancer.
Your new role
We are looking for a driven Ops Adv 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 driving force behind our production.
These are your responsibilities:
1. Leadership and supervision :
You will manage operational teams and supervise various operational units within the CAR-T production process.
2. 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.
3. Collaboration :
You are the first point of contact for production problems and work closely with other departments to find solutions.
4. Documentation management :
You will manage and review critical documentation within the production areas, such as procedures, work instructions, logs and transfer forms.
5. Batch record supervision:
You oversee the release and review of batch records for quality control.
6. Training:
As a manager, you make sure that everyone on your team gets the training they need to perform at their best.
7. Operational excellence:
You initiate projects that increase efficiency, reduce costs and improve quality.
You encourage and inspire your team to continuously improve.
Your profile
8. You have at least 3 years of experience in a GMP or ATMP environment, preferably in the biotech or pharmaceutical industry.
9. You have knowledge of cGMP regulations and clean room operations.
10. You can work fluently with Microsoft Office tools such as Word, Excel, PowerPoint and Outlook.
11. Experience with aseptic GMP production is a nice to have.
12. You have knowledge of cGMP regulations and clean room operations.
13. You can work fluently with Microsoft Office tools such as Word, Excel, PowerPoint and Outlook.
14. Familiarity with Manufacturing Execution Systems (MES) and Electronic Batch Record (EBR) systems is a plus.
Languages :
15. You speak and write English fluently.
Strengths :
16. You have excellent communication and organizational skills.
17. You are an empathetic people manager with strong leadership skills.
18. You have a positive attitude and
adapt easily to rapidly changing circumstances. You inspire others to do the same.
19. You are good at problem-solving, prioritizing and multitasking.
20. You have an eye for detail and procedures.
What you'll get in return
21. A meaningful job that contributes directly to the well-being of patients.
22. An excellent work-life balance. You work 4 days. Then you enjoy 4 days off.
23. A supportive and innovative work environment.
We value and encourage learning and personal development.
24. The opportunity to work with people from all over the world.
25. 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.
26. Many fun and informal events.
What you need to do now
Are you interested in this role? Please click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.
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