CAR-T Batch Release Specialist

Legend Biotech US

Oost-Vlaanderen

Sur place

EUR 60 000 - 90 000

Plein temps

14 jours+
Générateur de candidature

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Avantages offerts par ce poste

Meal vouchers
Group and hospitalization insurance
Double vacation pay
End-of-year bonus
Performance bonus
Additional statutory vacations

Résumé du poste

Legend Biotech in Ghent is seeking a Batch Release Coordinator to manage the timely manufacturing and release of patient-specific batches within our end-to-end supply chain. You will collaborate across Manufacturing, QA, QC and Investigations in a sterile GMP environment.

You will own BI dashboards and tools, diagnose data issues, and communicate progress to stakeholders. The role also supports detailed production planning and continuous improvement of reporting and analytics using Power BI and

Qualifications

  • Bachelor’s degree in supply chain, engineering, science or related field.
  • At least three years of experience in supply chain, operations or quality.
  • GMP pharma/biotech experience is a strong plus.
  • Hands-on with Power BI, Power Automate and other Microsoft tools.
  • Experience building and using complex Power BI dashboards from multiple data sources.

Responsabilités

  • Coordinate on-time batch release in collaboration with Manufacturing, QA, QC and Investigations.
  • Act as primary contact for stakeholders, ensuring clear and timely communication.
  • Maintain BI dashboards and troubleshoot data issues across sources.
  • Identify risks and bottlenecks and drive issue resolution.
  • Support master production scheduling and alignment with demand.
  • Contribute to continuous improvement of planning and reporting processes.

Connaissances

Power BI
Power Automate
Analytical thinking
Stakeholder 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

Legend Biotech in Ghent is seeking a Batch Release Coordinator to manage the timely manufacturing and release of patient-specific batches within our end-to-end supply chain. You will collaborate across Manufacturing, QA, QC and Investigations in a sterile GMP environment.

You will own BI dashboards and tools, diagnose data issues, and communicate progress to stakeholders. The role also supports detailed production planning and continuous improvement of reporting and analytics using Power BI and

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