Production Supervisor

Start People Belgium; Gent; Sur place; EUR 65 000 - 90 000; Plein temps

Avantages offerts par ce poste

Shift premiums

Meal vouchers

Group insurance

Hospitalization insurance

Double holiday pay

Year-end bonus

Performance bonus

4 days on/4 days off

Night shifts possible

Résumé du poste

Legend Biotech is seeking a Production Supervisor to oversee daily manufacturing of personalized CAR-T therapies, ensuring safe, compliant operations and cross-team coordination. From an office-base, you’ll maintain a clear overview of the production floor, driving collaboration and excellence.

You will lead multiple units, ensure quality systems, support GMP inspections, and foster a culture of continuous improvement with a patient-focused mindset.

Qualifications

• Bachelor’s or Master’s degree in Science, Bio-Engineering, Pharmacy, or related discipline.
• At least 3 years of experience in a production environment, preferably biotech/biopharma.
• Leadership experience as coordinator, supervisor, trainer or similar.
• Strong understanding of cGMP requirements and cleanroom operations.
• Experience with Microsoft Office; familiarity with MES and EBR systems is a plus.
• Excellent communication, organizational, and leadership skills with a people-focused approach.
• Flexible, positive, solution-oriented, with ability to manage multiple responsibilities and details.

Responsabilités

• Lead and supervise multiple operational units across CAR-T manufacturing processes.
• Act as the first contact for production issues and collaborate with cross-functional teams.
• Serve as SME for Quality and Operations within cGMP environments and support GMP inspections.
• Oversee quality-related production activities including document management and batch release.
• Coordinate quality system processes such as Change Controls, Deviations, Events and CAPAs.
• Ensure training and development support for the production team.
• Identify and implement production improvements to boost efficiency and quality.

Connaissances

Leadership

cGMP knowledge

Process coordination

Communication

Formation

Bachelor’s or Master’s degree in Science/Bio-Engineering/Pharmacy

Outils

MES

EBR

Microsoft Office

Description du poste

Production Supervisor - CAR-T Cell Therapy

At Legend Biotech, we're looking for a Production Supervisor to oversee the daily manufacturing of personalized CAR-T cell therapies for both clinical and commercial use.

In this role, you will lead key areas of the production process, ensure safe and compliant operations in line with cGMP requirements, and coordinate activities across multiple teams. From your office-based workspace, you'll maintain a clear overview of the production floor while driving seamless collaboration and operational excellence.

What you’ll do

• Lead and supervise multiple operational units across the CAR-T manufacturing process, including Component Preparation, Production Support, CAR-T Processing, Filling & Finishing, and Cryopreservation.
• Act as the first point of contact for production-related issues and collaborate closely with Manufacturing Operations, QC IPC, Quality, Facilities & Engineering, MS&T/Manufacturing Excellence, Training, Planning, and Supply Chain teams.
• Serve as a subject matter expert for Quality and Operations within cGMP-regulated environments and play a key role during GMP inspections and external audits.
• Oversee quality-related production activities, including documentation management, batch record review and release, and compliance with cGMP standards.
• Coordinate quality system processes such as Change Controls, Deviations, Events, and CAPAs.
• Ensure team members receive the appropriate training and support a culture of continuous development.
• Identify and implement improvement initiatives to enhance efficiency, quality, and overall operational performance.

Who we’re looking for

• Bachelor’s or Master’s degree in Science, Bio-Engineering, Pharmacy, or a related discipline, or equivalent experience.
• At least 3 years of experience within a production environment, preferably in biotech or biopharma.
• Previous leadership experience as a coordinator, supervisor, trainer or similar role.
• Strong understanding of cGMP requirements and cleanroom operations.
• Experience with Microsoft Office; familiarity with MES and EBR systems is considered an asset.
• Excellent communication, organizational, and leadership skills, combined with a people-focused and empathetic management approach.
• Flexible, positive, and solution-oriented, with the ability to prioritize effectively, manage multiple responsibilities, and maintain strong attention to detail.

What we offer

• The opportunity to make a real impact on patients’ lives through groundbreaking cell therapy treatments.
• A collaborative, innovative, and diverse working environment where learning and personal growth are encouraged.
• The chance to work alongside talented colleagues from around the world.
• A strong team culture with memorable events, celebrations, and plenty of legendary moments.
• A competitive salary package including shift premiums, meal vouchers, group insurance, hospitalization insurance, double holiday pay, year-end bonus, and performance bonus.
• A 4-days-on / 4-days-off schedule, supporting a healthy work-life balance.
• A combination of approximately two shifts, including openness to working night shifts.

Ready to make a difference?

If you’re looking for a leadership role where science, people management, and innovation come together, we’d love to hear from you.