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 QA Specialist, QA operations support, you will be part of the QA Support Team, responsible for projects and systems related to QA operation activities.

You will contribute to a multidisciplinary team related to improvement projects with responsibilities for providing quality oversight to support both clinical and commercial requirements in a sterile GMP environment.

Major Responsibilities

  • The QA Specialist, QA operations support will support projects and system governance in QA operation activities.
  • Contributes on the implementation and subsequent changes of a Manufacturing Execution System (MES) and / or implementation and subsequent changes of an Enterprise Resource Planning system (ERP)
  • Ensure appropriate support and governance of Master Data
  • Involvement in general QA operation/system projects
  • You are in close contact with multiple departments (Operations, Supply Chain, QC, QA, ...).
  • You will ensure accurate and timely review and approval of various testings of the system.
  • You will be responsible for drafting necessary documents, including Standard Operating Procedures and Work Instructions for the users.
  • Monitor and report on progress of the project goals and operational project KPIs
  • Review and approve standard operating procedures and batch records
  • Ensure accurate and timely maintenance and review of manufacturing investigations, CAPAs, change controls and complaints. Real time review of all documentation and reporting in support of process unit operations and release activities.
  • Strive to reduce non-conformances in supported areas by proactively driving compliance.
  • Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
  • Support regulatory inspections and audits by ensuring inspection readiness within facility.
  • Other duties will be assigned, as necessary.

Qualifications

Education: 

A minimum of a Bachelor’s Degree in Science, Engineering or equivalent technical discipline is required or relevant years of experience within the pharmaceutical industry.

Experience:

A minimum of 2 years relevant work experience is required. It is preferable that the candidate have experience in project management. Prior experience in pharmaceutical manufacturing or quality, is required

Key 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.
  • Must be able to create a highly collaborative and inclusive environment necessary for the team to be effective.
  • Knowledge of cGMP regulations and EMEA guidance related to manufacturing of cell-based products.
  • 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.
  • Ability to work in (transversal) teams - Team spirit.
  • Strong problem solving, pragmatic and positive critical thinking skills.
  • Can do attitude, right first time.
  • Great attention to detail and ability to follow the procedures.
  • The candidate must be highly organized and capable of working in a team environment with a positive attitude under minimal supervision. 
  • Good written and verbal communication skills are required. 
  • Ability to summarize and present results, and experience with team-based collaborations is a must. 
  • Must exhibit strong leadership skills and effectively develop others.
  • Ability to collaborate well with stakeholders, customers, and peers.
  • Must exhibit strong decision-making ability and think creatively while maintaining compliance and quality.
  • Must be able to discern the criticality of issues and to communicate to management regarding complex issues.
  • Ability to manage conflict and issues that arise with internal or external customers.

Language Requirements

Dutch and technical 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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