Job Information
J&J Family of Companies Logistiek Analyst in Antwerp, Belgium
Logistiek Analyst - 2406202401W
Description
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 patients 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 (-120C/-80C/2-8C)
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
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
Primary Location Europe/Middle East/Africa-Belgium-Antwerp-Beerse
Organization Janssen Pharmaceutica N.V. (7555)
Job Function Workday Associate B
Req ID: 2406202401W
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