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AstraZeneca

Global pharmaceutical company developing prescription medicines

Cell Development 1 Scientist - Process Development

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeShanghai, ChinaNo salary listedIn-person

About the Job

Requirements

  • A PhD or MSc in Cell Biology, Immunology, Molecular Biology, Bioengineering, Pharmacy, or a related field.
  • At least three years of industry experience in cell therapy process development.
  • Hands-on experience with large-scale, automated closed processes and multiple unit operations, including electroporation, cell expansion, and high-throughput fill-finish systems.
  • Hands-on experience developing and optimizing process parameters in representative small-scale models.
  • Proficiency with statistical analysis software such as JMP, Minitab, GraphPad Prism, or FlowJo.
  • Good English reading, writing, and speaking skills are required.

Responsibilities

  • Develop robust CAR-T manufacturing processes with in-depth experience in multiple unit operations, such as viral or non-viral gene delivery, large-scale expansion, and formulation.
  • Optimize critical process parameters and workflows to improve process performance and operational efficiency by designing and executing experiments, analyzing data, and providing science-based process-improvement insights using skills such as design of experiments, process analytical technology, and statistical modelling.
  • Drive platform evolution by exploring novel technologies and innovations, including industry trends, emerging methods, and best practices in cell therapy.
  • Analyze, document, and present experimental data and findings to internal teams and relevant stakeholders as needed.
  • Author and review technical documents such as batch records, process development reports, process transfer documents, and laboratory and equipment standard operating procedures.
  • Participate in laboratory operations and support team management to promote effective collaboration within and across teams.
  • Work with cross-functional stakeholders to transfer developed processes to manufacturing teams, providing process documentation, training, and technical support.
  • Support late-stage development for Investigational New Drug and Biologics License Application readiness, including process characterization, technical support for process performance qualification and clinical manufacturing, and regulatory-submission documentation.
  • Ensure data authenticity and compliance through comprehensive documentation, including databases, batch records, and other required technical records.

Desired Qualifications

  • Experience in both autologous and allogeneic CAR-T process development.
  • Demonstrated success in process scale-up and scale-down.
  • Proven success transferring a developed process to manufacturing.
  • Experience managing laboratory operations and teams.
  • End-to-end experience in Investigational New Drug or Biologics License Application projects.

About the Company

AstraZeneca

Global pharmaceutical company developing prescription medicines

AstraZeneca develops and markets prescription medicines and vaccines worldwide, with a focus on oncology, cardiovascular/metabolic, respiratory, and infectious diseases. Its products work by targeting specific biological pathways or cells, using small-molecule therapies, biologics, and vaccines to treat diseases or prevent infections. It differentiates itself through its dual heritage from Sweden and the UK, a broad pipeline, and strong R&D and collaborations that move from discovery to patient access. Its goal is to improve people’s health by discovering, developing, and delivering medicines and vaccines to patients worldwide.

Company size
10,001+
Company stage
IPO
Headquarters
Cambridge, United Kingdom
Founded
1913

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