EM/Logistic Analyst

☞ Johnson & Johnson

見る: 130

更新日: 02-12-2025

場所: Beerse Antwerp

カテゴリー: 経営管理 生産/操作

業界: Human Resources Services

レベル: Entry level

ジョブタイプ: Full-time

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仕事内容

Position Title: EM/Logistic analyst, QC CAR-T Europe

The Janssen Supply Chain Group, a member of the Johnson & Johnson family of companies, is recruiting an EM/Logistic analyst for the QC CAR-T hub in Europe. The position will be based in Beerse Belgium.

CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system. They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.

To support the CAR-T program in EMEA, Janssen has built two CAR-T manufacturing centers in the Ghent area (Belgium). The QC laboratories are located on the existing Janssen Beerse site.

The EM/Logistic analyst, QC CAR-T Europe is responsible for shipment of Environmental Monitoring samples, Drug Product samples and Critical Reagents. Next to that also the incubation and read-out of Environmental Monitoring samples will be part of your responsibilities. All activities should be following the applicable procedures, standards, and GMP regulations .

This job will be in a 2-shift regime: Early/Shifted late (6:00h-14:00h and 12:00h-20:00h)

Major Responsibilities

  • Environmental Monitoring testing:
    • Receival and unpacking of the shipment
    • Incubation
    • Read-out of results
    • Perform EM testing in compliance with all applicable specifications, procedures, GMP regulations
    • Drug Product Shipments, receival, unpacking and storage, including assigning the right storage locations to the different samples for all different temperature conditions (-120°C/-80°C/2-8°C)
    • On-Site transport of Critical Reagents
    • Copy of COA results in eLims for gowning, cleaning and other consumables
    • General administrative related QC tasks
    • Maintain a safe work environment in compliance with all applicable environmental, health, and safety regulations
    • Support laboratory related investigation records and CAPAs
    • Provide input to functional laboratory meetings
Qualifications:

  • A minimum of two (2) years of experience working in a cGMP compliant EM and or logistic function is required.
  • Experience in Environmental Monitoring testing is a plus.
  • Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint) is required.
  • Excellent written and oral communication skill are required
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締切: 16-01-2026

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