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CMC Project Management Intern

Somerset, 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 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 CMC Project Management Intern as part of the Technical Development team based in Somerset, NJ.

Role Overview

Legend Biotech is seeking an Intern as part of the CMC Project Management team based in Somerset, NJ}to support CMC (Chemistry, Manufacturing, and Controls) activities for our cell therapy programs. This role provides exposure to process development, analytical development, manufacturing, and quality control within a biotech environment. The intern will work closely with CMC project managers and technical leads to support program execution, timeline management, and cross-functional coordination across development and manufacturing activities.

Key Responsibilities

  • Support planning and execution of CMC activities across cell therapy programs, including process development, MSAT, analytical development, and manufacturing.
  • Assist in maintaining integrated CMC timelines, ensuring alignment across functional areas (PD, AD, QC, Manufacturing).
  • Track key milestones, deliverables, and critical path activities for development and GMP readiness.
  • Coordinate and document cross-functional CMC meetings (e.g., Technical Development Teams, CMC sub-teams).
  • Support risk identification and tracking, including development, manufacturing, and analytical risks.
  • Assist in developing and maintaining CMC project management tools (trackers, dashboards, Gantt charts).
  • Contribute to data organization and reporting, and development status summaries.
  • Support preparation of technical presentations and internal updates for program reviews.

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 organizational and time management skills with attention to detail.
  • Ability to understand and track technical development activities and dependencies.
  • Proficiency in Microsoft Excel and PowerPoint (experience with MS Project, Smartsheet, or similar tools is a plus).
  • Basic understanding of GMP principles and CMC development lifecycle preferred.
  • Strong written and verbal communication skills.

#Li-RP1

#Li-Hybrid

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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.

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I (the candidate) enter into this Non-Disclosure Agreement (the “Agreement”) with Legend Biotech USA Inc. (the “Company”), effective as of the date of my acknowledgement below, for the purpose of enabling the Company to evaluate a possible employment relationship with me.

  1. Access to Company Confidential Information. I acknowledge that for the sole and limited purpose of evaluating a possible employment relationship with me, the Company might disclose, or enable me to have access to, certain Confidential Information of the Company, as defined below.  I agree that, except for purposes of evaluating a possible employment relationship with the Company or as expressly authorized in writing by the Company, I will (a) not use or disclose any Confidential Information; (b) keep all Confidential Information confidential at all times; and (c) not copy, reproduce or modify any Confidential Information.
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  4. Remedies for Breach. I acknowledge that in the event of any breach of this Agreement, the Company will not have an adequate remedy in money or damages, and therefore the Company shall be entitled to obtain temporary, preliminary and/or permanent injunctive relief to redress any such breach, from any court of competent jurisdiction, and that the Company’s right to obtain such relief shall not limit its right to obtain other available remedies.
  5. General. The interpretation and enforcement of this Agreement shall be governed by the laws of the State of California.  This Agreement constitutes the entire agreement between the parties concerning the subject matters hereof; it supersedes any and all prior agreements or representations, written or oral, with respect to its subject matters; and it cannot be modified except in a written agreement signed by the Company.

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