Operations Support Specialist

Posted 9 Days Ago
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Raritan, NJ
1-3 Years Experience
Biotech
The Role
The Operations Support Specialist at Legend Biotech in Raritan, NJ, is responsible for supporting process operations in a sterile cGMP environment. Key responsibilities include performing support tasks, maintaining data records, building strong partnerships, and driving continuous improvements in cell therapy Technical Operations. The role requires a high school diploma with relevant experience, proficiency in computer skills, ability to work independently, and knowledge of cGMP regulations and FDA guidance.
Summary Generated by Built In

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 and natural killer (NK) cell-based immunotherapy. 

Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel) in 2017. Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.

Legend Biotech is seeking an Operations Support Specialist as part of the Technical Operations team based in Raritan, NJ.

Role Overview

The Operations Support Specialist will be part of the Technical Operations team responsible for the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment. Job duties will be performed within a team based on an assigned production shift schedule.

Key Responsibilities  

  • Support process operations by performing support specific and real time floor service tasks (i.e., kitting and kit cleaning, inventory management and data entry, sample management and data entry, aseptic behavior for cleaning of equipment, and cryopreservation) according to standard operating procedures and batch records, while recording production data and information in a clear, concise format.
  • Perform tasks on time in a manner consistent with safety policies, quality systems, and cGMP requirements.
  • Build strong partnerships with Manufacturing, Warehouse, Engineering, and Quality, and work as part of a cross-functional team to complete production tasks required by shift schedule.
  • Support the development of manufacturing processes, and will work with others to drive continuous improvements and efficiencies within cell therapy Technical Operations.

Requirements

  • H.S. Diploma with relevant experience required; or Certificate or Associates degree in a scientific or health services field preferred, Bachelor’s degree in a scientific or health services field preferred.
  • A minimum of 0-1 years of Operations experience within a cGMP environment in the biotech/biopharma industry.
  • Proficient computer skills to be able to navigate specialized software and databases.
  • An ability to build strong partnerships and effectively integrate with external collaborators to drive projects/programs forward in a matrixed environment.
  • Ability to work independently and successfully, prioritize and manage multiple tasks simultaneously, integrate cross-functional issues and balance competing priorities effectively.
  • Clear and succinct verbal and written communication skills with an attention to detail and the ability to follow procedures.
  • Knowledge of cGMP regulations and FDA guidance related to manufacturing of cell based products.
  • Ability to lift a minimum of 50 lbs. and stand for a long period of time.
  • Sufficient vision and hearing capability to work in job environment with physical dexterity sufficient to use computers and document production records.
  • Ability to handle human derived materials in BSL-2 cleanroom facility.
  • Physical dexterity sufficient to use computers and documentation.
  • Ability to accommodate shift work including evenings and weekends as required by the manufacturing process.
  • Ability to accommodate unplanned overtime on little to no prior notice.

#Li-Onsite

#Li-JT1

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.

The Company
HQ: Somerset, New Jersey
1,192 Employees
On-site Workplace
Year Founded: 2014

What We Do

Legend Biotech is a global, commercial-stage biotechnology company developing and manufacturing novel therapies. We explore and apply innovative technologies to deliver cutting-edge options for patients around the world.

Our corporate headquarters is located in Somerset, NJ, and our manufacturing footprint includes facilities in the United States, China and the Belgium.

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