Associate Director, Cell Therapy Discovery

AstraZeneca

Shanghai, China
Cell therapy process development and cmc
Lvv upstream and downstream process development
Cell based assay establishment and validation
AstraZeneca’s Cell Therapy R&D is dedicated to discovering, engineering, and developing next generation cellular therapies to address high unmet medical needs across the clinical portfolio

Job Summary

  • AstraZeneca’s Cell Therapy R&D is dedicated to discovering, engineering, and developing next generation cellular therapies to address high unmet medical needs across the clinical portfolio.
  • The role involves leading innovative cell therapy science for engineered CAR-T products targeting solid and hematologic tumors, integrating process development and CMC considerations.
  • The position requires collaboration with internal and external partners to drive technology transfer, scale-up, and clinical supply while ensuring compliance with AstraZeneca policies and applicable laws.

Matching Summary

AstraZeneca’s Cell Therapy R&D is dedicated to discovering, engineering, and developing next generation cellular therapies to address high unmet medical needs across the clinical portfolio.

Skills & Requirements

Must-have

  • Cell therapy process development and CMC
  • LVV upstream and downstream process development
  • Cell based assay establishment and validation
  • Gene editing and CAR-T engineering
  • Cross-functional project execution
  • Virus analytical method qualification
  • Compliance with GxP and manufacturing regulations

Nice-to-have

  • Independent project initiation and execution
  • Strong interpersonal and collaboration skills
  • Proficient English communication and writing
  • Knowledge of regulatory frameworks for cell/gene therapies
  • Understanding of CQAs/CPPs and DoE process characterization

Key Requirements

  • Masters or PhD in Cell/Molecular Biology or related field
  • Demonstrable experience in cell therapy PD and CMC
  • Hands-on experience with LVV process development and CAR-T manufacturing
  • Proven track record in analytical method validation for cell therapy
  • Experience collaborating with CDMOs and external suppliers
  • Knowledge of GxP and laboratory/manufacturing regulations

Work Rights

Not specified

Tailored Resume

Cover Letter