Cell Therapy Supply Chain Logistics Associate

Há 21 horas


Taperoá, Brasil Nexcella, Inc. Tempo inteiro

Cell Therapy Supply Chain Logistics AssociateNexcella, Inc.Sao Paulo / HybridOur 3 Core Values- Intelligence- Integrity- InitiativeWhat You'll DoOverseeing the patient journey from screening through treatment across CAR-T therapies You will work cross-functionally with internal and external stakeholders to ensure therapies reach patients as quickly and efficiently as possible.Key ResponsibilitiesYou will play a key role in supporting our Global Patient Supply Operations:- Work cross functionally between clinical operations, manufacturing, and quality to effectively manage patient products from leukapheresis collection through drug- product infusion- Develop and improve SOPs, work instructions, and training materials which are used to ensure seamless end to end patient journey- Manage logistics providers which are responsible for transportation of patient- material (starting material, intermediates, and final product)- Ensure chain of custody (COC) and chain of Identity (COI) measures are maintained throughout all patient journey activities- Support CMO activities which includes logistics support for all patient related- material including CMO storage capacity management- Support/manage clinical sites as primary point of contact (POC) for scheduling and- general inquiries regarding patient journey activitiesQualifications- Bachelor's or Master's degree in relevant discipline (or equivalent experience)- 1-5 years of work experience or the equivalent combination of education and- experience- Previous industry experience in a biotech or pharma companyAbout Nexcella, Inc.Nexcella, Inc. is a subsidiary of Immix Biopharma, Inc. (ImmixBio) (Nasdaq:IMMX), a clinical-stage biopharmaceutical company developing cell therapies for AL Amyloidosis and other serious diseases.
Our lead candidate is sterically-optimized BCMA-targeted chimeric antigen receptor T (CAR-T) cell therapy NXC-201 with a "digital filter" that filters out non-specific activation.
NXC-201 is being evaluated in the U.S. multi-center study for relapsed/refractory AL Amyloidosis NEXICART-2 (NCT06097832), with a registrational design.
Interim results were presented at ASCO 2025 in an oral presentation by Heather Landau, M.D. of Memorial Sloan Kettering Cancer Center.
NXC-201 has been awarded Regenerative Medicine Advanced Therapy (RMAT) by the US FDA and Orphan Drug Designation (ODD) by FDA and in the EU by the EMA.
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