Posted:
8/27/2024, 7:46:29 AM
Location(s):
New Jersey, United States
Experience Level(s):
Mid Level ⋅ Senior
Field(s):
Consulting
Workplace Type:
Hybrid
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 a QC Analytical Methods Expert (Consultant) as part of the Global MSAT team based in Raritan, NJ.
Role Overview
This position represents a critical technical role supporting analytical automation efforts within the global MSAT organization. The candidate must have strong laboratory skills, bioassay, cell biology and immunology experience. This individual will be providing specialist knowledge and expertise of cell and gene therapy analytical methods, for a commercially approved product. Specifically, this effort will include scope related to both flow and plate based analytical assays and will help design the automation platform that integrates with eLIMS and MES to manage samples from manufacturing in cGMP through final testing results. The scope comprises of defining changes to current analytical methods to enable automation integration to identifying new technologies for all release assays to reduce sample time and increase throughput for a future business state. Expertise is also required in managing and implementing transfers of qualified, validated and comparable test methods approved for the commercial program. This position will actively interact with internal MFG/AD/QC/QA team and external client SMEs to develop and drive the strategy and supporting business cases to ensure the successful delivery of a commercial CARVYKTI automation platform. The ideal candidate for this position should have work experience in cell therapy process development, manufacturing science, analytical development, and familiarity with GMP/FDA/ICH .
Key Responsibilities
#Li-hybrid
#Li-JK2
#contract
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.
Website: https://legendbiotech.com/
Headquarter Location: Piscataway, New Jersey, United States
Employee Count: 1001-5000
Year Founded: 2014
IPO Status: Public
Last Funding Type: Post-IPO Equity
Industries: Biotechnology ⋅ Health Care ⋅ Life Science ⋅ Oncology ⋅ Therapeutics