Associate Director, Global Strategic Operations & Capacity Planning Head
Raritan, NJ, United States
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 Associate Director, Global Strategic Operations & Capacity Planning Head as part of the Technical Operations team based in Raritan, New Jersey.
Role Overview
This position is a key member in the global MSAT organization leadership team. This individual will be responsible for a global operational strategy and investigations lead / owner for a best-in-class high volume marketed CAR-T product as part of a multi-site global manufacturing network. This individual is required to manage a global strategic operations to ensure that available and future capacity can meet forecasted demand. Strategic planning is required to identify and implement operational improvements, capacity expansion/optimization, cost of goods / non-conformance reduction and improved turnaround times worldwide. Additional responsibilities will be providing technical content/strategics plans as part of collaborative working groups with cross functional partners (i.e. and competitiveness) to develop process automation and improve delivery/logistics to patient (i.e.. reduce TAT) allowing Legend to maintain a competitive advantage in the market place.
Key Responsibilities
Additional responsibilities include;
* Management oversight and/or contribute to strategic capacity plans and competitiveness (COGs reduction/TAT/OOS reduction), global investigations, global metrics reporting and systems* Co-Facilitates complex global investigation and OOS reduction efforts with partner. Drives recommendation, plans and implements changes/ improvements and ensures continuity amongst sites and external CMO partners* Drives plans and technology integration for facility infrastructure and determines optimal approaches for which to maximize utilization and capacity to meet global demand and commercial forecasts* Drives and prioritizes operations improvement (closed process, streamlined operations) implementation, collaborates on new automation technology platforms to determine appropriate global implementations plans* Develops technical content/strategic plans and collaborates to improve delivery/logistics to patient (ie. reduce TAT) to maintain competitive advantage* Develops Data Analytics & Global Reporting structure and identifies appropriate business systems and tools to ensure effective reporting across sites and external CMO partners* Develops business processes, charters working groups and establishes governance and RACIs for global initiatives (ie. global investigation lifecycle; strategic capacity planning working groups; OOS and TAT strategic working groups)* Drives solutions to complex manufacturing operations issues at internal and external manufacturing sites* Develops strategic plans and business cases to meet to meet key business metrics (ie. capacity build/utilization/outsource, second sourcing, etc.)* Collaborates and ensures alignment with key cross-functional stakeholders and partners (ie. supply chain, quality, alliance mgmt., finance, operations, MFG leadership and commercial)
Requirements
* B.S. required, Ph.D. preferred in technical discipline: engineering, science, or related field.* Minimum 8+ years of industrial biologics CMC development or manufacturing experience, CAR-T experience is highly desirable.* Extensive experience in cell therapy commercial cGMP operations with end-to-end know-how to drive changes/improvements and capacity plans in a global manufacturing network.* Candidate must have extensive experience in Cell Therapy tech transfer and/or MSAT.* Experience in a cross functional commercial team in driving global programs and/or initiatives.* Experience in implementing and managing commercial process improvements and changes and leading complex investigations.* Experience in driving consistency across multiple manufacturing sites.* Extensive knowledge in cell therapy operations, technology transfer, investigations, capacity/throughput studies, strategic capacity upgrades.* Ability to think critically and demonstrated troubleshooting and problem-solving skills.* Results driven with strong analytical, problem solving and critical thinking skills.* Strong experience working in a cross-functional organization with multiple partners with competing priorities.* Ability to plan, multitask, prioritize and be an effective and influential decision maker focused on action and implementation.
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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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