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:
- 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.
Your profile
- You have at least 3 years of experience in a GMP or ATMP environment, preferably in the biotech or pharmaceutical industry.
- You have 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 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 English fluently.
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 you'll get in return
- 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.
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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