QC Stability Coordinator Intern
Company: Legend Biotech
Location: Somerset
Posted on: April 2, 2026
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Job Description:
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
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Keywords: Legend Biotech, Philadelphia , QC Stability Coordinator Intern, Science, Research & Development , Somerset, Pennsylvania
