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CAR-T is an innovative blood cancer treatment that uses the strength of the patient' s own immune system. The patient' s T-cells are genetically modified to eliminate the cancer cells. This advanced technology offers hopeful prospects to patients for whom other therapies provide no or insufficient results.

We are therefore working passionately on expanding our capacity for CAR-T treatments in Europe, both at our existing site in Beerse and in Ghent, where we have developed a new production site. We are looking for strong talents who are eager to participate in this innovative and hopeful venture.

The Innovative Medicine Supply Chain Group, a member of the Johnson & Johnson family of companies, is therefore recruiting an eLIMS associate for the CAR-T hub in Europe. The position will be based in Beerse Belgium.

The eLims associate, CAR-T Europe is responsible for providing first line eLims/iLabs support for Ghent & Beerse. They will be responsible for drawing eLims set-up including LME / reagent module & instrument module set-up for the Ghent & Beerse labs in accordance with Janssen policies, standards, procedures, and Global cGMP’s.

Major Responsibilities:

• Setup and create user accounts for colleagues within the Ghent and Beerse sites
• Setup and maintain eLims for analysis performed at the Ghent and Beerse labs, including spec, sample plan and sample flows.
• Support the iLabs module including LME module, instrument module and reagent module for the Ghent and Beerse labs.
• Support EMS related eLims master data including schedulers, work items.
• Support in reviewing and updating SOPs, WIs and Protocols to support LME, reagent module & instrument module implementations using the Document Management System
• Responsible for providing training & access in the eLims system
• Responsible for User acceptance testing in case of any changes in the eLims system

Experience and Skills:

• A minimum of a bachelor’s degree in Engineering, Science or equivalent technical field is required.
• A minimum of 1 years of experience in an eLims or equivalent system role
• Knowledge of cGMP regulations and FDA/EU mentorship is a plus.
• Excellent IT and administration skills are required.
• Excellent written and oral (Dutch and/or English) communication skills are required.#RPOAMS