Legend Biotech Corporation
Operations Support Specialist, 1st Shift
Legend Biotech Corporation, Raritan, New Jersey, us, 08869
Operations Support Specialist, 1st Shift
Raritan, New Jersey, United States 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, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize cilta-cel. 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
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. Schedule: Sun-Wed, 1st Shift 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. Qualifications and Requirements
H.S. Diploma with relevant experience required; or Certificate or Associate’s 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 navigate specialized software and databases. Ability to build strong partnerships and effectively integrate with external collaborators to drive projects/programs forward in a matrixed environment. Ability to work independently, prioritize and manage multiple tasks simultaneously, integrate cross-functional issues and balance competing priorities effectively. Clear and succinct verbal and written communication skills with attention to detail and the ability to follow procedures. Knowledge of cGMP regulations and FDA guidance related to manufacturing cell-based products. Ability to lift a minimum of 50 lbs. and stand for extended periods. Sufficient vision and hearing capability to work in a job environment with physical dexterity to use computers and document production records. Ability to handle human-derived materials in a BSL-2 cleanroom facility. 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. Base pay range: $46,467 - $60,989 USD Benefits and EEO
We are committed to creating a workplace where employees can thrive—both professionally and personally. We offer a comprehensive benefits package designed to support well-being, financial stability, and long-term career growth. Highlights include medical, dental, and vision insurance; a 401(k) plan with company match; equity and stock options for eligible roles; paid parental leave; paid time off (vacation, personal, sick days, holidays, and floating holidays); and various supplemental benefits. Legend Biotech is an equal opportunity/affirmative action employer. Employment is at-will and Legend may adjust compensation at any time. Legend Biotech maintains a drug-free workplace. Apply for this job
This refined description excludes the full application form content for brevity and clarity.
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Raritan, New Jersey, United States 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, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize cilta-cel. 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
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. Schedule: Sun-Wed, 1st Shift 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. Qualifications and Requirements
H.S. Diploma with relevant experience required; or Certificate or Associate’s 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 navigate specialized software and databases. Ability to build strong partnerships and effectively integrate with external collaborators to drive projects/programs forward in a matrixed environment. Ability to work independently, prioritize and manage multiple tasks simultaneously, integrate cross-functional issues and balance competing priorities effectively. Clear and succinct verbal and written communication skills with attention to detail and the ability to follow procedures. Knowledge of cGMP regulations and FDA guidance related to manufacturing cell-based products. Ability to lift a minimum of 50 lbs. and stand for extended periods. Sufficient vision and hearing capability to work in a job environment with physical dexterity to use computers and document production records. Ability to handle human-derived materials in a BSL-2 cleanroom facility. 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. Base pay range: $46,467 - $60,989 USD Benefits and EEO
We are committed to creating a workplace where employees can thrive—both professionally and personally. We offer a comprehensive benefits package designed to support well-being, financial stability, and long-term career growth. Highlights include medical, dental, and vision insurance; a 401(k) plan with company match; equity and stock options for eligible roles; paid parental leave; paid time off (vacation, personal, sick days, holidays, and floating holidays); and various supplemental benefits. Legend Biotech is an equal opportunity/affirmative action employer. Employment is at-will and Legend may adjust compensation at any time. Legend Biotech maintains a drug-free workplace. Apply for this job
This refined description excludes the full application form content for brevity and clarity.
#J-18808-Ljbffr