CAR-T Batch Release Coordinator

LegendBiotech; Belgique; À distance; EUR 65 000 - 95 000; Plein temps

Avantages offerts par ce poste

Meal vouchers

Group health insurance

End-of-year bonus

Professional development

Résumé du poste

Legend Biotech is seeking a Production Scheduler & BatchTracking Specialist to coordinate timely manufacturing and release of patient-specific batches in a GMP environment. You will collaborate with Manufacturing, QA, QC and Investigations to ensure smooth operations across the supply chain.

You will build detailed production schedules, translate demand forecasts into feasible plans, and maintain BI dashboards to monitor batch status.

Qualifications

• Bachelor’s degree in relevant field or equivalent experience.
• At least three years of experience in supply chain, operations or quality.
• GMP experience in pharma or biotech is a strong plus.
• Hands-on experience with Power BI, Power Automate and other Microsoft tools.

Responsabilités

• Coordinate on-time release of batches with Manufacturing, QA, QC and Investigations.
• Serve as main contact for stakeholders and provide updates on batch status.
• Maintain and enhance BI dashboards to support batch release coordination.
• Build detailed production schedules and translate demand forecasts into plans.

Connaissances

Stakeholder coordination

Analytical thinking

Multi-priority management

English fluency

Formation

Bachelor’s degree in Supply Chain, Engineering, Science or related field

Outils

Power BI

Power Automate

Microsoft Excel

Description du poste

Do you enjoy coordinating complex processes, connectingstakeholdersand ensuring a smooth manufacturingand releaseprocess?As we continue to expand our operations inGhent, we are looking for a Production Scheduler & Batch Tracking Specialistto join ourSupply Chainteam. In this role, you will play a keyrolein deliveringCAR-Tcell therapies – making a direct impact on patients’ lives.

What can you expect?

As a Production Scheduler & Batch Tracking Specialist, you are responsible for coordinating the timely manufacturing and release of patient-specific batches within our end-to-end supply chain. You ensure smooth collaboration across teams in a sterile GMP environment.Youare responsible for;

Batch Coordination & Stakeholder Management

• Coordinating the on-time release of finished product batches in close collaboration with Manufacturing, QA, QC, and Investigations teams
• Acting as the primary point of contact for stakeholders, ensuring clear andtimelycommunication
• Providing transparent updates on batch status, progress, and challenges
• Building strong relationships across internal and external stakeholders
• Owning,maintainingand enhancing the BI dashboards and tools to support batch release coordination
• Acting as a primary point of contact for BI dashboards troubleshooting by diagnosing and resolving issues across the dashboard landscape, ranging from minor defects and data-quality concerns to complex problems involving data models, refreshes,integrationsor performance
• Proactivelyidentifyingrisks and bottlenecksimpactingbatch release timelines
• Driving discussions to resolve issues and ensure continuity
• Escalating critical risks and supporting decision-making at theappropriate level

Planning

• Building detailed production schedules to ensure timely execution of manufacturing activities while maximizing capacity utilization and minimizing disruptions
• Contributing to the execution of the master production plan by translating demand forecasts into feasible short- and mid-term production schedules
• Collaborating with planning, manufacturing and warehouse teams to align supply with clinical and commercial demand
• Driving process improvements and contributing to reporting and scalable planning methodologies

Who are we looking for?

Education

• You obtained abachelor’s degree in Supply Chain, Engineering, Science or a related field or have equivalentexperience

Experience

• You haveat least three years of relevant experience in supply chain,operationsor quality
• Experience in a GMP environment within pharma or biotech is a strong plus
• You have hands‑on experience with Power BI, Power Automateand other Microsoft tools to support reporting analytics,automationor business processes
• You have experience with building and using complex Power BI dashboards, combining multiple data sources

Languages

• You are fluent in English

Strengths

• You have strong analytical and problem-solving skills
• You havestrong communicationskills that foster collaboration and set clear expectations
• Youare abletocoordinate complex processes and manage multiple priorities
• Youare abletostay calm, focussed and motivated under tight deadlines
• You are tech savvy and like to explore new ways to automatic analytics and business processes

What do we offer you?

• A meaningful job where you contribute to patients’ lives.
• 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 packagecomplemented by many fringe benefits, such asadditionalstatutory vacations, meal vouchers, group and hospitalization insurance, double vacation pay, an end‑of‑year and performance bonus.
• Many fun and informal events.

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.