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:

  • 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.


#LI-DNI
Cliquez-ici pour accéder à la Politique de confidentialité de Hays, qui vous apportera des informations détaillées sur la manière dont nous utilisons et protégeons vos données personnelles et vos droits relatifs à ces données.

Résumé

Type d'emploi
CDI
Secteur
Healthcare & Medical
Lieu
Zwijnaarde
Spécialité
Life Sciences management
Salaire
A contract of indefinite duration and an attractive salary package complemented
Réf. :
1108337

Contacter un consultant

Contactez Audrey Melis, le consultant en charge de cette offre d'emploi, situé à Ghent
Hays Ghent, Kortrijksesteenweg 1084

Téléphone: 032027976

Numéro d'agrément 


VG 292/BUOSA W.INT.35 W.SO.35 


Brussels n° 00322-406-20121217 

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