EM/Logistic analyst, QC CAR-T Europe

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Job Function:

Non-Standard

Job Sub Function:

Workday Associate B

Job Category:

Non-Standard

All Job Posting Locations:

Beerse, Antwerp, Belgium

Job 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 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

The anticipated base pay range for this position is:

€0.00 - €0.00

Benefits:

In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees' and companies' performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being re