Logistiek Analist (Vroege verlegde late )

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 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 patients 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 (-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 and requirements:

• 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 skills in Dutch are required

At Johnson & Johnson we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear fair and respectful of your time.

Heres what you can expect:

• Application review: Well carefully review your CV to see how your skills and experience align with the role.

• Getting to know you: If theres a good match youll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.

• Staying informed: We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.

• Final steps: For successful candidates you will need to complete country-specific checks before starting your new role. We will help guide you through these.

Finally at the end of the process well invite you to share feedback in a short survey your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. Were excited to learn more about you and wish you the best of luck in the process!

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