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.

About the position: 

The Operations Investigation Expert will be part of the Operations project team and has the mission to:

  • Support and execute investigations within Operations (production).
  • Participate in multidisciplinary investigations teams as appropriate and/or establish strategy to quickly driving to root cause to meet critical release windows (the highest priority being safe and timely product release for the patient).
  • Own the investigation process and methodologies for operational investigations, create awareness and educate the operations organization on the importance of and how to adequately and efficiently handle quality investigations in time.
  • Properly apply processes and standards and support the implementation of CAPAs related to the manufacturing process together with other impacted departments as needed.
  • Act as operations SPOC for Regulatory Authorities inspection of investigational Operations subjects, accountable to defend the strategy, investigation reporting and potential answer to observations that he/she managed or coordinated.
  • Build solid and long-lasting connections with different stakeholders to ensure smooth alignment and handling of complex investigations, while acting as the operations single point of contact.

Contribute to building operations, scientific and cGMP capability/expertise within the operations investigations team, focused on cell and gene therapy processes and/or process technologies, to thrive improvement of Product Quality, Safety and Efficacy.

Responsibilities: 

  • Operations expertise:
    • Continuously gather the operational knowledge of the cell and gene therapy manufacturing process technology to provide expertise input during operational investigations.
    • Learn the entire production process on the shopfloor to be able to perform adequate investigations.
    • Participate in multi-disciplinary investigations and provide operational input needed for sub-parts of any investigation.
  • Quality & Compliance:
    • Understand and implement the importance of GMP aspects in your investigations.
    • Take the lead in investigating and reporting deviations regarding GMP.
    • Support other departments in investigating deviations related to other aspects of production (process, QA, QC,…) as needed.
    • Participate in applying and implementing appropriate risk assessment methodologies and root cause analysis tools and assess product quality impact.
    • Stay up to date with GMP/regulatory requirements and state of the art guidelines, maintain permanent inspection readiness, actively support regulatory inspections and preparation thereof as SME, and support the implementation of actions resulting from such inspections.
    • Draft, feed, review/revise, and/or support writing of (not limited to):
      • Investigations (incl. impact and risk assessments, corrections, CAPAs)
      • Change controls
    • Continuously maintain compliance with internal training requirements.
    • Recognize and act on potential compliance issues and opportunities for process changes/improvement.
    • Act as operations SPOC for Regulatory Authorities inspection of operational subject, accountable to defend the strategy, investigation reporting and potential answer to observations that he/she managed or coordinated.
  • Continuous Improvement:
    • Support the implementation of quality investigation resulting CAPAs related to the manufacturing process.
    • To further maintain and lead the investigation dashboard and supporting QEM systems and identify opportunities for improvement.
    • Ensure connection between recurrent deviations and process robustness activities, perform trending, and feed the organization based on lessons learned from investigations.
  • Development/Role Specific:
    • Build strong partnerships in a matrixed environment, i.a. by liaising with different internal cross-functional teams such as MS&T, QC (IPL), Supply Chain, Engineering and Quality, as well as effectively integrating with external collaborators, to drive projects/programs forward and ensure efficient execution of process validation and production schedules (clinical and commercial).
    • Ensure seamless flow of knowledge and information across functions, departments, and with other sites when applicable, resulting in fast and effective resolution of issues.

Qualifications:

  • A minimum of a Master’s degree in (bio)-Engineering, Science, Pharmacy or related field or equivalent experience required.
  • A minimum of 3-5 years of Project execution experience within operations or within a cGMP or ATMP environment in the biotech/biopharma industry. Prior experience in manufacturing, quality or engineering is a must.
  • Knowledge of cGMP regulations and FDA/EU guidance related to ATMPs.
  • Ability to work independently and successfully under minimal supervision and integrate cross-functional issues and balance competing priorities effectively.
  • Self-motivated, enthusiastic personality, team player, with a desire to learn new skills.
  • Excellent scientific writing skills with an attention to detail.
  • Being able to manage shifting priorities and multiple tasks simultaneously to meet critical deadlines in a fast paced and dynamic, growing environment.
  • Flexible mindset capable to deal with ambiguity and to respond quickly, energetically, and enthusiastically to changes.
  • Positive and pro-active attitude.
  • Results driven while working within GMP framework of procedures and rules.
  • Excellent organizational skills.
  • Strong analytical mind, problem solving and critical thinking skills. Being able to trouble shoot and resolve complex scientific/technical problems.
  • Advanced computer skills and practical knowledge.
  • Clear communicator with ability to build strong partnerships.
  • Dutch/English 

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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