EM/Logistic analyst - early-shifted late

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:
Non-Standard

Job Sub Function:
Workday Associate B

Job Category:
Non-Standard

All Job Posting Locations:
Beerse, Antwerp, Belgium

Job Description:

About Innovative Medicine  

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.

Visionaries like you work on teams that save lives by developing the medicines of tomorrow. 

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. 

Learn more at https://www.jnj.com/innovative-medicine 

About CAR-T

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.

We are searching for the best talent for a EM/Logistic analyst - early-shifted late, to be in Beerse.

 

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)

You will be responsible for:


* Environmental Monitoring testing: Receival and unpacking of the shipment, incubation, read-out of result


* 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 laborat...