Legend Biotech US
Overview
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 is seeking
Production Scheduler Supervisor
as part of the
Technical Operations
team based in
Raritan, NJ . Role Overview This role operates within Technical Operations with responsibility for supporting Capacity Planning, Production Planning, and Detailed Scheduling activities, enabling Raritan short-range planning and daily manufacturing execution for Clinical, Commercial, and Study/Development production runs. The individual will collaborate with various Technical Operations groups (e.g., Operations, MS&T, Supply Chain) and Quality functions to lead all planning and detailed scheduling activities for Operators, Production Slots, QPIP, Equipment Cleaning, facility maintenance, and related areas. Responsibilities Participate in Vein-to-Vein, S&OP (CRR), Site Supply Chain, and Operations meetings (e.g., Production Ramp Up plan) to assess manufacturing constraints and prioritize site production targets. Facilitate evaluation of pre-requisites for capacity protocol development and study/development runs with the site cross-functional team. Support and coordinate raw material release status, PO status, and documents to ensure on-time production schedule execution. Develop and maintain functional stakeholder relationships to assemble and execute an optimized, aligned schedule. Monitor day processing activities against the scheduling plan and address ERP issues related to Sales Orders, Process Orders, and Code Conversions. Track progress-to-plan, identify risks to the production schedule, and align stakeholders to develop solutions. Run reports to verify schedules for impacted areas. Work with facility and metrology teams to ensure efficient scheduling of equipment PMs and Cals while supporting the manufacturing plan. Lead material allocation improvements and other optimization projects. Build strong partnerships and effectively integrate with external collaborators to drive projects/programs forward in a matrixed environment. Work independently, prioritize and manage multiple tasks, and balance cross-functional issues and competing priorities. Maintain clear and succinct verbal and written communication with attention to detail and adherence to procedures. Knowledge of supply chain principles (materials management, distribution, import/export, transportation), pharmaceutical operations, and industry practices. Knowledge of cGMP regulations and FDA guidance related to manufacturing of cell-based products. Support as required by manufacturing and support area processes. Promote a mindset of continuous improvement, problem solving, and prevention. Requirements
Bachelor’s degree in Supply Chain Management, Business/Engineering, or related field or equivalent work experience required. A minimum of 6 years working within supply chain/operations. Operations experience within a cGMP environment in the biotech/biopharma industry is preferred. SAP and/or Oracle experience. Technologically savvy with the ability to quickly adopt new systems and processes. Proficient in Excel (Pivot Tables and Advanced Analytics), Word, Visio, and exposure to ERP and other financial accounting systems. Transparent, Passionate, Fearless and Accountable. Compensation : The anticipated base pay range is $81,273 - $106,669 USD. Benefits and Workplace
We are committed to creating a workplace where employees can thrive—both professionally and personally. We offer a best-in-class benefits package that supports well-being, financial stability, and long-term career growth, including medical, dental, and vision insurance; a 401(k) plan with company match; equity and stock options for eligible roles; paid parental leave; and a comprehensive paid time off policy. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, disability coverage, and various supplemental plans. We also provide commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs. EEO Statement
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 applicable law. Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company. Legend Biotech maintains a drug-free workplace. Apply for this job
To apply, please visit Legend Biotech’s careers site. This posting summarizes the key responsibilities and qualifications; for the complete details, refer to the official job posting.
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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 is seeking
Production Scheduler Supervisor
as part of the
Technical Operations
team based in
Raritan, NJ . Role Overview This role operates within Technical Operations with responsibility for supporting Capacity Planning, Production Planning, and Detailed Scheduling activities, enabling Raritan short-range planning and daily manufacturing execution for Clinical, Commercial, and Study/Development production runs. The individual will collaborate with various Technical Operations groups (e.g., Operations, MS&T, Supply Chain) and Quality functions to lead all planning and detailed scheduling activities for Operators, Production Slots, QPIP, Equipment Cleaning, facility maintenance, and related areas. Responsibilities Participate in Vein-to-Vein, S&OP (CRR), Site Supply Chain, and Operations meetings (e.g., Production Ramp Up plan) to assess manufacturing constraints and prioritize site production targets. Facilitate evaluation of pre-requisites for capacity protocol development and study/development runs with the site cross-functional team. Support and coordinate raw material release status, PO status, and documents to ensure on-time production schedule execution. Develop and maintain functional stakeholder relationships to assemble and execute an optimized, aligned schedule. Monitor day processing activities against the scheduling plan and address ERP issues related to Sales Orders, Process Orders, and Code Conversions. Track progress-to-plan, identify risks to the production schedule, and align stakeholders to develop solutions. Run reports to verify schedules for impacted areas. Work with facility and metrology teams to ensure efficient scheduling of equipment PMs and Cals while supporting the manufacturing plan. Lead material allocation improvements and other optimization projects. Build strong partnerships and effectively integrate with external collaborators to drive projects/programs forward in a matrixed environment. Work independently, prioritize and manage multiple tasks, and balance cross-functional issues and competing priorities. Maintain clear and succinct verbal and written communication with attention to detail and adherence to procedures. Knowledge of supply chain principles (materials management, distribution, import/export, transportation), pharmaceutical operations, and industry practices. Knowledge of cGMP regulations and FDA guidance related to manufacturing of cell-based products. Support as required by manufacturing and support area processes. Promote a mindset of continuous improvement, problem solving, and prevention. Requirements
Bachelor’s degree in Supply Chain Management, Business/Engineering, or related field or equivalent work experience required. A minimum of 6 years working within supply chain/operations. Operations experience within a cGMP environment in the biotech/biopharma industry is preferred. SAP and/or Oracle experience. Technologically savvy with the ability to quickly adopt new systems and processes. Proficient in Excel (Pivot Tables and Advanced Analytics), Word, Visio, and exposure to ERP and other financial accounting systems. Transparent, Passionate, Fearless and Accountable. Compensation : The anticipated base pay range is $81,273 - $106,669 USD. Benefits and Workplace
We are committed to creating a workplace where employees can thrive—both professionally and personally. We offer a best-in-class benefits package that supports well-being, financial stability, and long-term career growth, including medical, dental, and vision insurance; a 401(k) plan with company match; equity and stock options for eligible roles; paid parental leave; and a comprehensive paid time off policy. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, disability coverage, and various supplemental plans. We also provide commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs. EEO Statement
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 applicable law. Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company. Legend Biotech maintains a drug-free workplace. Apply for this job
To apply, please visit Legend Biotech’s careers site. This posting summarizes the key responsibilities and qualifications; for the complete details, refer to the official job posting.
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