CAR-T QC & Environmental Logistics Analyst Europe 2-Shift

Biopharma Careers

Antwerpen

Hybride

EUR 42 000 - 54 000

Plein temps

14 jours+
Générateur de candidature

Une candidature sur mesure pour ce poste — un CV personnalisé et une lettre de motivation qui correspondent directement à l’offre.

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Résumé du poste

Johnson & Johnson is seeking an EM/Logistic Analyst within QC CAR-T Europe to support Environmental Monitoring with careful sample handling and data integrity. The role includes processing Drug Product samples under strict temperature controls and coordinating reagent logistics to ensure GMP compliance.

You will work across teams, handle administrative QC tasks in eLIMS, and participate in CAPA activities, safety initiatives and meetings. Shift work is required (early/late).

Qualifications

  • Min. 2 years in a cGMP environment with Environmental Monitoring or logistics.
  • Experience with Environmental Monitoring tests is a strong plus.
  • Good knowledge of GMP guidelines and compliance procedures.
  • Excellent administrative and documentation skills.

Responsabilités

  • Receive, unpack, incubate and read Environmental Monitoring samples per GMP.
  • Perform Environmental Monitoring tests and accurately report results.
  • Receive, process, store and manage Drug Product samples at -120°C, -80°C and 2-8°C.
  • Coordinate internal transport of Critical Reagents and support material flow.
  • Maintain administrative QC tasks, including COA results in eLIMS.
  • Support laboratory investigations, CAPAs, safety initiatives and meetings.

Connaissances

GMP compliance
Environmental Monitoring
Logistics coordination
Documentation
QC collaboration
Two-shift work
Microsoft Office
E-LIMS
Excel

Outils

eLIMS
Excel

Description du poste

Johnson & Johnson is seeking an EM/Logistic Analyst within QC CAR-T Europe to support Environmental Monitoring with careful sample handling and data integrity. The role includes processing Drug Product samples under strict temperature controls and coordinating reagent logistics to ensure GMP compliance.

You will work across teams, handle administrative QC tasks in eLIMS, and participate in CAPA activities, safety initiatives and meetings. Shift work is required (early/late).

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