Cell Therapy Supply Chain Logistics Associate

2 semanas atrás

São Paulo, São Paulo, Brasil Nexcella, Inc. Tempo inteiro
Cell Therapy Supply Chain Logistics Associate
Nexcella, Inc.

Sao Paulo / Hybrid

Our 3 Core Values
Intelligence
Integrity
Initiative

What You'll Do
Overseeing 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 Responsibilities
You 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 activities

Qualifications
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 company

About 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. Learn more at and

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