R&D Applications Specialist

Legend Biotech
Location
Somerset, New Jersey, United States
Job Type
Full-time
Posted
September 1, 2026
Views
10

Job Description

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of serious diseases. From our global network of research and development sites, we are committed to discovering and developing safe, effective, and cutting-edge therapies for patients worldwide.

Legend Biotech entered into a global collaboration agreement with Johnson & Johnson to jointly develop and commercialize CARVYKTI® (ciltacabtagene autoleucel; cilta-cel). Through this strategic partnership, we combine complementary expertise and capabilities to advance innovative immunotherapies for patients living with multiple myeloma.

Legend Biotech is seeking anR&D Applications Specialistas part of theInformation Technologyteam based inSomerset, NJ.

Role Overview

The R&D Applications Specialist will assist in the operation of laboratory IT capabilities and R&D systems. This individual’s responsibility will include operation maintenance and implementation/development of enhancements of applications that are used in the R&D laboratories.

Key Responsibilities

  • Administrating and maintaining Equipment/Asset Platform (Blue Mountain RAM), LIMS/ELN (Labvantage) and various other lab applications used in R&D.
  • Configure/enhance BMRAM as per business requirements. Maintain and support the system and ensure that it is compliant.
  • Configure/develop enhancements to LabVantage LIMS/ELN system as per business requirements. Create and maintain master data/static data in lab systems by executing the appropriate change management process to support laboratory testing activities and to ensure business, project and/or investigation/CAPA timelines are met. Review method/specification changes and work with appropriate SMEs to assess impact to lab systems data set up.
  • Aid in troubleshooting and assist in technical support of both instrument software installed on lab computers and connectivity between computer and instrument.
  • User account provisioning on stand-alone and networked equipment and instruments.
  • User account provisioning on scientific software (e.g., FlowJo, Zageno, SnapGene, Journal Subscriptions, etc.).
  • Collaborate/liase with appropriate laboratory, manufacturing, analytical support and/or site/global IT teams to ensure needs and requirements are accurate in the systems.
  • Contribute to team success by assisting colleagues with assigned work activities and deliverables, ensuring timely and effective execution of team responsibilities.
  • Test changes/enhancements through dry runs, system test and user acceptance test.
  • Evaluate, recommend and implement processes to improve compliance and the efficiency of laboratory testing operations (i.e visibility to testing queues, testing metrics monitoring, etc) to support product release, new products, and key performance indicators/lean lab metrics.
  • Execute and document appropriate change control and/or verify changes executed by team members are accurate.
  • Author, revise, and/or review procedural documents, such as SOP sand WIs and contribute to the development of associated training content.
  • Provide support for internal compliance and regulatory agency inspections as required.
  • Respond to system issues and troubleshoot to identify root cause.
  • Provide support and systems management of R&D applications and lab computing environment in accordance with IT Policies and Procedures.
  • Coordinate the necessary risk assessment and qualification protocols to support the GxP applicability of systems
  • Track, document, and update incidents and requests accurately in the IT Service Management (ITSM) system
  • Assist in updating any knowledge base articles.
  • Maintain a willingness to learn new skills, processes, and technologies, and participate in training activities as directed to support individual and team success.

Requirements

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of serious diseases. From our global network of research and development sites, we are committed to discovering and developing safe, effective, and cutting-edge therapies for patients worldwide.

Legend Biotech entered into a global collaboration agreement with Johnson & Johnson to jointly develop and commercialize CARVYKTI® (ciltacabtagene autoleucel; cilta-cel). Through this strategic partnership, we combine complementary expertise and capabilities to advance innovative immunotherapies for patients living with multiple myeloma.

Legend Biotech is seeking anR&D Applications Specialistas part of theInformation Technologyteam based inSomerset, NJ.

Role Overview

The R&D Applications Specialist will assist in the operation of laboratory IT capabilities and R&D systems. This individual’s responsibility will include operation maintenance and implementation/development of enhancements of applications that are used in the R&D laboratories.

Key Responsibilities

  • Administrating and maintaining Equipment/Asset Platform (Blue Mountain RAM), LIMS/ELN (Labvantage) and various other lab applications used in R&D.
  • Configure/enhance BMRAM as per business requirements. Maintain and support the system and ensure that it is compliant.
  • Configure/develop enhancements to LabVantage LIMS/ELN system as per business requirements. Create and maintain master data/static data in lab systems by executing the appropriate change management process to support laboratory testing activities and to ensure business, project and/or investigation/CAPA timelines are met. Review method/specification changes and work with appropriate SMEs to assess impact to lab systems data set up.
  • Aid in troubleshooting and assist in technical support of both instrument software installed on lab computers and connectivity between computer and instrument.
  • User account provisioning on stand-alone and networked equipment and instruments.
  • User account provisioning on scientific software (e.g., FlowJo, Zageno, SnapGene, Journal Subscriptions, etc.).
  • Collaborate/liase with appropriate laboratory, manufacturing, analytical support and/or site/global IT teams to ensure needs and requirements are accurate in the systems.
  • Contribute to team success by assisting colleagues with assigned work activities and deliverables, ensuring timely and effective execution of team responsibilities.
  • Test changes/enhancements through dry runs, system test and user acceptance test.
  • Evaluate, recommend and implement processes to improve compliance and the efficiency of laboratory testing operations (i.e visibility to testing queues, testing metrics monitoring, etc) to support product release, new products, and key performance indicators/lean lab metrics.
  • Execute and document appropriate change control and/or verify changes executed by team members are accurate.
  • Author, revise, and/or review procedural documents, such as SOP sand WIs and contribute to the development of associated training content.
  • Provide support for internal compliance and regulatory agency inspections as required.
  • Respond to system issues and troubleshoot to identify root cause.
  • Provide support and systems management of R&D applications and lab computing environment in accordance with IT Policies and Procedures.
  • Coordinate the necessary risk assessment and qualification protocols to support the GxP applicability of systems
  • Track, document, and update incidents and requests accurately in the IT Service Management (ITSM) system
  • Assist in updating any knowledge base articles.
  • Maintain a willingness to learn new skills, processes, and technologies, and participate in training activities as directed to support individual and team success.

Requirements

  • BS degree with 3-5 years experience in Biotech/Pharmaceutical industry.
  • An understanding of laboratory science in the life sciences industry, preferably in cell therapy space.
  • Understanding of GxP software administration and configuration.
  • Installing, configuring and supporting systems and applications in lab environments.
  • Experience with direct customer/user interaction, including training.
  • Demonstrate an understanding of the need for standards yet also have a willingness to look for new, more effective strategies to support and improve the laboratory computing environment.
  • Experience supporting standalone or enterprise computerized systems and/or applications.
  • Commitment to Quality.
  • Problem solving skills.
  • Ability to work on multiple complex projects where independent action and a high degree of initiative are required in resolving problems and developing recommendations
  • Demand Management Skills - Ability to take initiative and prioritize objectives from multiple tasks; adhere to scheduled timelines while maintaining flexibility, independently or as part of a team. Self-directed with a high degree of professional integrity, very organized, and detail oriented.
  • Familiarity with ticketing systems (ServiceNow, Jira, or similar)..
  • Must have knowledge of software development lifecycle (SDLC) and of computer systems validation (CSV)
  • Proficient knowledge and understanding of Microsoft Office Applications (Access, Excel, Project, PowerPoint, SharePoint, Teams, Word) and/or other relevant software programs.
  • Strong interpersonal, oral and written communication skills, and service-oriented attitude are essential. Must contribute to a team based, collaborative and positive environment, clarity of purpose and high commitment to business goals.

#Li-FB1

#Li-Hybrid

The base pay range below is what Legend Biotech USA Inc. reasonably expects to offer at the time of posting. Actual compensation may vary based on experience, skills, qualifications, and geographic location. The company reserves the right to modify this range as needed and in accordance with applicable laws.

Other Types of Pay: Performance-based bonus and/or equity is available to employees in eligible roles.

Benefits and Paid Time Off: Medical, dental, and vision insurance as well as a 401(k) retirement plan ...

Frequently Asked Questions

Where is the job located, and is it remote/hybrid/on-site?
The position is based on-site in Somerset, New Jersey, United States.
What are the required qualifications and experience level for this role?
Candidates must have a BS degree with 3-5 years of experience in the Biotech/Pharmaceutical industry. You need an understanding of laboratory science (preferably in cell therapy), GxP software administration/configuration, and experience installing, configuring, and supporting systems in lab environments.
What are the key responsibilities of the R&D Applications Specialist?
You will administer and maintain laboratory IT capabilities and R&D systems, including Blue Mountain RAM and LabVantage LIMS/ELN. Responsibilities include configuring system enhancements, provisioning user accounts, troubleshooting instrument software and connectivity, executing change controls, and authoring procedural documents like SOPs.

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Job Information

Source: greenhouse
AI Relevance: 60/100 (Relevant)
Remote Type: onsite
Allowed Locations: Somerset, New Jersey, United States
Skills & Tags:
R&D Systems

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