QC Stability Coordinator Intern

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 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. Legend Biotech is seeking a QC Stability Coordinator as part of the Technical Development team based in Somerset, NJ. Role Overview Legend Biotech is seeking an Intern as part of the Analytical Development team based in Somerset, NJ to assist in the planning, execution, and documentation of stability studies to support pipelines. This role provides hands-on experience in laboratory operations, stability data trending, documentation, and compliance with regulatory guidelines. Key Responsibilities Oversee the scheduling, pulling, and testing of stability samples across internal and external QC labs. Maintain accurate and contemporaneous records in Quality Management Systems and in a verified database for internal stakeholders. Conduct stability trending analysis from analytical results for review by QC manager or SME. Assist in preparing charts, graphs, and preliminary reports and be able to deliver within the targeted timeline. Participate in team meetings and provide updates on assigned tasks. Requirements Currently enrolled in a U.S. college or university program (Chemistry, Biology, Pharmaceutical Sciences, or related field). Basic understanding of laboratory procedures and scientific data handling. Strong attention to detail and organizational skills. Proficiency in Microsoft Excel and/or

SMARTSHEET.

Excellent written and verbal communication skills Ability to work independently and as part of a team. Motivated, highly organized and muti-tasking skills Ability to learn and understand scientific data in Cell and Gene Therapy settings. #Li-RP1 #Li-Hybrid #Li-Contract Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech. EEO Statement It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances. Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company. For information related to our privacy notice, please review: Legend Biotech Privacy Notice.