Job Description
<div class="content-intro"><p style="line-height: 1.2;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">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 RD sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.</span></p>
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<p style="line-height: 1.2;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">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). 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.</span></p>
<p style="line-height: 1.2;"> </p></div><p class="col-xs-12 no-horiz-padding"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Legend Biotech is seeking an <strong>Operational Excellence Lead, Execution</strong> as part of the <strong>Technical Operations </strong>team based in <strong>Raritan, NJ.</strong></span></p>
<p><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"><strong>Role Overview</strong></span></p>
<p><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">This position will be responsible for providing operational excellence leadership to the cGMP Commercial Cell Therapy Manufacturing plant. This individual will partner with Raritan Site Leadership Team and various Technical Operation and Quality functions to support cell therapy operations through safe and compliant methodologies according to cGMP requirements. The role will require proven leadership and expertise that drives effective communication, coordination and collaboration across relevant cross functional groups to establish a strong continuous improvement and problem-solving culture and project management to enable robust production, testing and release of product to patients.</span></p>
<p><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"><strong>Key Responsibilities</strong></span></p>
<ul>
<li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Plans, leads, develops, provides expertise, trains, coaches, drives and manages an effective, holistic continuous improvement, problem solving and to improve safety, compliance, cost, process stability build quality and efficiency into processes to improve lead times and reliability to deliver products to patients.</span></li>
<li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Implement a continuous improvement program using lean and six sigma manufacturing methodologies such as standardized work, daily management system (e.g. tier process), metrics, visual tools, PDCA, Kanban, pull systems, SMED, pareto, FMEA and others.</span></li>
<li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Implement the routine use of disciplined problem solving such as DMAIC.</span></li>
<li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Develop, teach, implement and coach the effective use of tools such as kata methodology, A3 thinking, 4Ups, 6S and oth ... (truncated, view full listing at source)