QC CAR-T Logistics Analyst Europe (2-Shift)

Johnson & Johnson Innovative Medicine; Beerse; Sur place; EUR 45 000 - 60 000; Plein temps

Avantages offerts par ce poste

Two-shift schedule

GMP compliant environment

Résumé du poste

Johnson & Johnson in Beerse, Belgium, invites applications for an EM/Logistic Analyst within QC CAR-T Europe. The role focuses on Environmental Monitoring sample handling, testing, and compliant documentation in a GMP environment.

You will manage Drug Product samples, Critical Reagents, and administrative QC tasks in a two‑shift setting. Collaborate with cross‑functional teams to ensure proper sample treatment, storage and traceability, while supporting CAPAs and safety initiatives.

Qualifications

• Minimum 2 years of experience in a cGMP environment within Environmental Monitoring, logistics or a similar role.
• Experience with Environmental Monitoring tests is a strong plus.
• Good knowledge of GMP guidelines and working to quality/compliance procedures.

Responsabilités

• Receive, unpack, incubate and read Environmental Monitoring samples according to GMP guidelines and procedures.
• Perform Environmental Monitoring tests and correctly register and report results.
• Receive, handle, store and manage Drug Product samples under different temperature conditions (-120°C, -80°C and 2-8°C).
• Coordinate internal transport of Critical Reagents and support raw material flow.
• Manage administrative QC tasks, including processing COA results in eLIMS for gowning, cleaning and other consumables.
• Support laboratory investigations, CAPAs, safety initiatives and contribute to functional laboratory meetings.

Connaissances

EM Experience

Logistics

GMP/Quality

MS Office

Documentation

Communication

eLIMS

Outlook

Excel

Word

PowerPoint

Outils

eLIMS

Outlook

Excel

Word

PowerPoint

Description du poste

Johnson & Johnson in Beerse, Belgium, invites applications for an EM/Logistic Analyst within QC CAR-T Europe. The role focuses on Environmental Monitoring sample handling, testing, and compliant documentation in a GMP environment.

You will manage Drug Product samples, Critical Reagents, and administrative QC tasks in a two‑shift setting. Collaborate with cross‑functional teams to ensure proper sample treatment, storage and traceability, while supporting CAPAs and safety initiatives.