CAR-T production supervisor

LegendBiotech; Oost-Vlaanderen; Sur place; EUR 90 000 - 120 000; Plein temps

Avantages offerts par ce poste

Meal vouchers

Group and hospitalization insurance

End-of-year bonus

Performance bonus

Company laptop

Résumé du poste

Legend Biotech is seeking a CAR-T production supervisor to lead a motivated team of operators in a cleanroom, ensuring GMP-compliant operations and high-quality output. You will guide daily activities, foster growth, and maintain top quality levels while solving challenges as they arise.

You will oversee core production steps, manage documentation, and drive continuous improvement in collaboration with cross-functional teams. Fluency in English and a strong leadership mindset are essential.

Qualifications

• Bachelor’s or Master’s degree in science, bi o-engineering, pharmacy or related field or equivalent by experience.
• Experience in people leadership in a regulated environment or at least 3 years in GMP/ATMP environment with leadership.
• Knowledge of cGMP regulations and clean room operations is a plus.
• Proficient with Microsoft Office tools (Word, Excel, PowerPoint, Outlook).
• MES and EBR systems experience is a plus.

Responsabilités

• Lead and inspire operational teams and oversee key steps in the CAR-T production process.
• Manage all aspects of quality and ensure strict cGMP compliance and support GMP inspections.
• Collaborate with other departments to resolve production challenges and implement improvements.
• Maintain and review critical documentation like procedures, work instructions, logs and transfer forms; oversee release and review of batch records for quality control.

Connaissances

People leadership

GMP/ATMP knowledge

English fluency

Problem solving

Formation

Bachelor's or Master’s in science/related

Outils

Microsoft Office

MES

Electronic Batch Record (EBR)

Description du poste

Are you ready to take the lead in one of the most innovative fields in biotech? As a CAR-T production supervisor at Legend Biotech, you’ll lead a motivated team of operators in a cleanroom facility, ensuring smooth operations and a high standard of quality from start to finish. You’ll help make sure that daily activities run smoothly, safely, and in line with GMP standards. You’ll be guiding your team with all the responsibilities that come with it: facilitating growth of your team, inspiring them in their daily tasks and maintaining quality levels, and solving problems as challenges arise.

What Can You Expect?

As CAR-T production supervisor, you’ll be the driving force behind our operations. Your responsibilities will include:

• Leading & inspiring: manage operational teams and oversee key steps in the CAR-T production process.
• Ensuring quality: 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.
• Collaborating & solving: you’ll be the go-to person for production challenges and work closely with other departments to find solutions.
• Keeping us organized: manage and review critical documentation like procedures, work instructions,logsand transfer forms.You’llalso oversee the release and review of batch records for quality control.
• Training & developing talent:asa manager,you’llmake sure your team has the skills and knowledge to excel.
• Driving operational excellence: launch projects to boost efficiency, cut costs, and improve quality.Inspirecontinuousimprovementeveryday.

Who Are We Looking For?

Education

• 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.

Experience

You have either:

• Experience in people leadership in a regulated environment,
• Or at least 3 years of experience in a GMP or ATMP environment (preferably in the biotech or pharmaceutical industry), and a drive for the new challenge of leading a team.

Expertise

• Comfortable with Microsoft Office tools such as Word, Excel, PowerPoint and Outlook.
• Manufacturing Execution Systems (MES) and Electronic Batch Record (EBR) systems experience is a plus.
• Knowledge of cGMP regulations and clean room operations is a plus.

Languages

• You speak and write fluent English.

Strengths

• Excellent communication and organizational skills.
• Empathetic leader with strong people management abilities.
• Positive, adaptable, and inspiring under rapidly changing circumstances.
• Skilled at problem solving, prioritizing and multitasking.
• Detail-oriented and process-driven.

What Do We Offer?

• A meaningful job that contributes directly to the well-being of patients.
• Anexcellent work-life balance. You work 4 days. Then you enjoy 4 days off.
• Asupportive and innovative work environment. We value and encourage learning and personal development.
• The opportunity towork with people from all over the world.
• A contract of indefinite duration andan 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.
• Manyfun and informal events
• A permanent contract of indefinite duration and an attractive salary package complemented by a wide range of fringe benefits, including additional statutory holidays, meal vouchers, company laptop, smartphone and subscription, net allowance, group and hospitalization insurance, double holiday pay, end-of-year bonus, performance bonus and the possibility to participate in our bicycle lease plan.

Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend’s policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.

Legend Biotech maintains a drug-free workplace.

With over 2,900 employees worldwide, Legend Biotech is the largest standalone cell therapy company and a pioneer in treatments that are changing cancer care for good. We develop and market the CAR-T cell therapy ciltacabtagene autoleucel (cilta-cel) in partnership with ohnson & Johnson. In the EU, cilta-cel is approved under the brand name CARVYKTI® for the treatment of adult patients with relapsed and refractory multiple myeloma who have received at least one prior line of therapy.

Legend Biotech is a fully integrated global organization with manufacturing sites in the United States and Europe. From our sites in Ghent, Belgium, our teams support the clinical and commercial supply of CAR-T therapies across the EMEA region, translating advanced science into real-world impact for patients.

What sets us apart is clarity of purpose. At Legend Biotech Europe, everyone understands how their role contributes to our mission and how their daily work helps bring life-changing therapies to patients who need them most.