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

As Project Builder, you will be part of the MES Project Team, responsible for modelling the electronical batch records. This in support of the daily CAR-T operations and production to timely support (i) clinical and (ii) commercial readiness and (iii) commercial CAR-T product supply to both Europe and US. You will work in the GMP Facility in Ghent and report to the MES Project Lead. The position offers a perfect environment to understand Manufacturing Operations and all the underlying Supply Chain systems around it (Planning, Quality, Distribution, EHS…).

Responsibilities

  • You are responsible for the integration of Manufacturing/Operational/Process knowledge into various building blocks which together form the new Master Batch Record (MBR)
  • You strive to achieve standardization within the different building blocks of the MBR
  • You are in close contact with multiple departments (Operations, MS&T, QA, Engineering & Maintenance, etc.) to discuss and build the ideal sequence of MES building blocks in order to deliver an MES system in the most user-friendly way.
  • You decide in which way various parameters are secured in the MBR for a specific recipe, making sure quality of the product is guaranteed.
  • You make sure implementation of building blocks and changes afterwards are executed in a correct and validated manner. Correct documentation (i.e. specifications, protocols and reports) will be key.
  • You will be involved in the execution of various testing of the system including UAT’s.
  • You will be responsible for drafting necessary documents, including Standard Operating Procedures and Work Instructions for the users.
  • You will be involved in the training of the users
  • You will support system integrations such as SAP, eLIMS, Data Lake, OSI PI…
  • You will serve as SME to support various projects/initiatives requiring Manufacturing data
  • You are responsible to work in a constructive and flexible way, this in a team based and cross functional environment

Qualification

Education:

  • Graduate, Bachelor’s or Master’s degree in Science, Bio-Engineering, BioTechnology,Pharmacy or related field or equivalent experience required

Experience:

  • A minimum of 1-year hands on operations experience within a cGMP or ATMPenvironment in the biotech/biopharma industry is preferred 
  • Minimum 1-year hands-on experience in aseptic techniques in clean rooms is preferred
  • Knowledge of GMP is preferred
  • Experience in manufacturing, maintenance, quality, testing, or engineering areas is preferred

Capabilities, Knowledge, and skills

  • Ability to work independently and successfully, prioritize and manage multiple tasks simultaneously, integrate cross-functional issues and balance competing priorities effectively.
  • Strong influence and relationship building skills with an emphasis on teamwork
  • In-depth understanding of function and application of product
  • Clear and succinct verbal and written communication skills with an attention to detail and the ability to follow procedures.
  • Knowledge of cGMP regulations and EMEA guidance related to manufacturing of cell-based products.
  • Focus on quality, compliance and detail
  • Ability to work in (transversal) teams - Team spirit
  • Strong problem solving, pragmatic and positive critical thinking skills
  • Can do attitude, right first time
  • Self-motivated, enthusiastic personality, team player with a desire to learn new skills
  • Flexible mindset capable to deal with ambiguity and to respond quickly, energetically, and enthusiastically to changes
  • Self-motivated, enthusiastic personality, team player, with a desire to learn new skills and train juniors 

Language

Dutch and English

#LI-AG1

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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