Company Information

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.  

Legend Biotech entered into a global collaboration agreement with Janssen Biotech, Inc. to develop, manufacture and commercialize ciltacabtagene autoleucel (cilta-cel). Through our strategic partnership, we look to advance the promise of an immunotherapy in the treatment of multiple myeloma.

Role Overview

The QC Support technician, CAR-T Manufacturing is an executing function with responsibilities within QC area related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment.

Major Responsibilities:

You will support the daily QC analyses: 

• You will control, disinfect and clean the materials/equipment needed for the QC analyses.

• You will help out with the internal transfer of the materials from the logistic center to the in process lab.

 • You will help out with the handling of the waste from the lab.

• You will support the transport of the samples (QC release, QC retain, EM) at different temperatures (room temperature, cooled transport).

• You will support the EM analyses in grade C and grade D.

• You will utilize an electronic system (LIMS) for execution and accurate documentation of the disinfection and cleaning of the equipment or document your performed tasks in a correct way in logbooks and forms.

 - You execute the activities in a strictly regulated environment.

 - You perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.

 - Other duties will be assigned, as necessary

Qualification

Education:

A2 Degree or equivalent experience required

Experience:

No experience is required.

Capabilities, Knowledge, and skills:

  • The candidate must be highly organized, responsible, structured, punctual and capable of working in a highly regulated, aseptic environment with a positive attitude under supervision.
  • The candidate must be able to work in an ordered, planned way.
  • The candidate must be able to follow procedures, the fixed way to handle the tasks in a GMP environment.
  • Communicate on a structured way with your colleagues and supervisor.
  • Candidates must be able to accommodate shift schedule. Shifts include routine weekend and evening work as required by the manufacturing process.
  • Candidates must be able to accommodate unplanned overtime (including nights) on little to no prior notice.
  • You have a A2 Degree, or equivalent experience. The quality mindset and accuracy are more important than degree or qualification.

Language(s):

Dutch and/or English

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Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend’s policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.

Legend Biotech maintains a drug-free workplace.

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