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.

Position Overview

This position will be part of the CAR-T Asset Management team within the Technical Operations group and will be responsible for taking up Subject Matter Expert (SME) responsibilities for assets within the cGMP Clinical and Commercial Cell Therapy Manufacturing plants in Ghent (Belgium). Next to this main focus, this position will take the lead in or support in continuous improvement projects. This individual will be responsible for handling day-to-day activities inclusive of qualification management, vendor management, issues, deviations, corrections and remediation efforts for production process and lab equipment and systems (assets) in support of personalized cell therapy production through safe and compliant manufacturing operations according to cGMP requirements. This role will require project management skills, C&Q and general engineering experience, ability to work independently, drive effective communication, coordination and collaboration across relevant cross functional groups to establish a strong, compliant engineering program to enable robust production, testing and release of product to patients.  

Major Responsibilities
  • Acts a subject matter expert (SME) for assigned assets within the plants
  • Acts as an administrator for assigned systems within the plants and is responsible for follow-up on user access requests
  • Responsible for timely execution of Periodic Audit Trail Review and User Access Review
  • Responsible for timely execution of Periodic System Quality Reviews and takes action accordingly
  • Participates in authoring and reviewing CARA documents (Critical Aspects Risk Assessments), T&TM’s (Test & Traceability Matrices), Project Plans and Master Plans
  • Participates in authoring and reviewing C&Q protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria, specifically data integrity.
  • Supports and reviews the commissioning, qualification, requalification and any associated engineering activities within the plants.
  • Manages multiple and complex engineering projects, provides status reports and coordinates with other departments or outside contractors/vendors to complete tasks.
  • Supports and/or owns technical and quality investigations related to assets
  • Develops and performs any required remediation efforts and associated CAPA plans.
  • Executes, owns, assesses and participates in the creation, revision and review of change controls, SOPs, and other documentation.
  • Participation in operational meetings
Qualification
 
Education: 

A minimum of a Master’s Degree in Science, Engineering, Bioengineering or equivalent technical discipline is required.

Experience:
 
A minimum of 2 years relevant work experience within a cGMP environment. It is preferable that the candidate has experience working in an Aseptic manufacturing facility.
 
 
Capabilities, Knowledge, and skills:
  • Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell-based products as well as knowledge of Good Tissue Practices.
  • A good understanding of technical installations, P&IDs, equipment, and (computerized) systems within the Life Science Industry.
  • Strong interpersonal and written/oral communication skills.
  • Ability to quickly process complex information and often make critical decisions with limited information.
  • Ability to independently be responsible for a portfolio of ongoing projects.
  • Ability to pay attention to details and follow the procedures.
  • The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision.
  • Good written and verbal communication skills are required.
  • Ability to summarize and present results, and experience with team-based collaborations is a requirement.
  • Proficient in applying process excellence and QRM tools and methodologies.
  • Ability to identify/remediate gaps in processes or systems.
  • Experience authoring and executing documentation including but not limited to: (electronic) batch records, SOPs, Work Instructions, C&Q protocols.
  • Experience with ERP (SAP), CMMS (SAP PM), QTS (TrackWise) and DMS/LMS is preferred.
Language(s):
Dutch/English
 
#LI-AG1
 
#LI-Onsite

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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