AstraZeneca

AstraZeneca

Posted via Workday

Cell Development l Scientist, Process Development

Apply by Dec 31, 2026

Posted Sep 8, 2026

Role at a glance

Salary
Checking details Salary details are being checked. See the description for the employer's terms.
Location
Shanghai, Guilin Road
Work arrangement
On-site
Employment
Full-time
Experience
Checking details Experience requirements are being checked. See the qualifications below.
Education
PhD or MSc in Cell Biology, Immunology, Molecular Biology, Bioengineering, Pharmacy, or related fields.

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Role Summary

AI-generated

The role develops and improves CAR-T manufacturing processes, from process development through transfer to manufacturing. It also supports late-stage development and regulatory readiness.

What You'll Do

  • Develop CAR-T manufacturing processes and optimize critical parameters and workflows through experiment design, execution, and data...
  • Explore novel technologies, emerging methods, industry trends, and best practices in cell therapy.
  • Analyze, document, and present experimental findings; author and review technical records, reports, transfer documents, and SOPs.
  • Support lab operations and collaboration within and across teams, while ensuring data authenticity and complete technical records.
  • Transfer developed processes to manufacturing teams through detailed documentation, training, and technical support.
  • Support late-stage development, including process characterization, PPQ and clinical manufacturing support, and regulatory submission...

Generated from the employer's posting. Verify important details before applying.

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Qualifications

PhD or MSc in Cell Biology, Immunology, Molecular Biology, Bioengineering, Pharmacy, or a related field; minimum of 3-year 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 in development and optimization of process parameters in representative small-scale models; creative and proactive, able to identify and address issues; demonstrated ability to collaborate efficiently with cross-function teams; good English reading, writing, and speaking skills.

Preferred

  • Experience in both autologous and allogeneic CAR-T process development is a plus.
  • Demonstrated success in process scale-up and scale-down is preferred.
  • Proven success of transferring developed process to manufacturing is a plus.
  • Proficiency with statistical analysis software (e.g., JMP/Minitab/GraphPad Prism /Flowjo) is highly desired.
  • Experience in management of lab operation and team management is a plus.
  • End-to-end experience in IIT, IND or BLA projects is a plus.

Original job description

Content provided by the employer

Major responsibilities    

  • Develop robust CAR-T manufacturing process with in-depth experience in multiple unit operations (e.g., viral/non‑viral gene delivery, large scale expansion, formulation).
  • Optimize critical process parameters and workflow to improve process performance and facilitate operation efficiency, including designing and executing experiments, analyzing data, and providing science-based insight for process improvement with application of professional skills such as DoE, PAT (process analytical technology) and statistical modelling.
  • Drive platform evolution via exploring novel technologies and innovations (i.e. industry trends, emerging methods, and best practices in the area of 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, laboratory and equipment SOPs.
  • Take a role in lab operation and support team management to promote high-efficiency collaboration within and across teams.
  • Work closely with cross-function stakeholders to facilitate smooth transfer of developed processes to manufacturing teams, providing detailed process documents, training, and technical support.
  • Support late-stage development for IND/BLA readiness such as process characterization, providing technical support for PPQ and clinical manufacturing, documentation for regulatory submission.
  • Ensure data authenticity and compliance with comprehensive documentation including databases, batch records, and other required technical records.

Education, Qualifications, Skills and Experience

  • PhD or MSc in Cell Biology, Immunology, Molecular Biology, Bioengineering, Pharmacy, or related fields.
  • Minimum of 3-year industry experience in cell therapy process development. Experience in both autologous and allogeneic CAR-T process development is a plus.
  • Hands-on experience with large-scale, automated closed processes and multiple unit operations, including electroporation, cell expansion, and high-throughput fill-finish systems. Demonstrated success in process scale-up and scale-down is preferred.
  • Hands-on experience in development and optimization of process parameters in representative small-scale models. Proven success of transferring developed process to manufacturing is a plus.
  • Proficiency with statistical analysis software (e.g., JMP/Minitab/GraphPad Prism /Flowjo) is highly desired.
  • Experience in management of lab operation and team management is a plus.
  • Creative thinker and proactive doer that can identify and effectively address issues and gaps.
  • Demonstrated ability to collaborate efficiently with cross-function teams to drive project move forward.
  • End-to-end experience in IIT, IND or BLA projects is a plus.
  • Good English skills in reading, writing and speaking is a must.

Date Posted

08-Sept-2026

Closing Date

30-Dec-2026

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

AstraZeneca

About the company

AstraZeneca

Large Enterprise

AstraZeneca is a global biopharmaceutical company dedicated to the research, development, and commercialization of innovative medicines. Headquartered in Cambridge, UK, the company focuses on areas such as oncology, cardiovascular, renal, metabolism, and respiratory diseases, striving to deliver life-changing treatments to patients. With a strong commitment to scientific excellence and collaboration, AstraZeneca invests in cutting-edge technologies and partnerships to drive advancements in healthcare. The company is also committed to sustainability and corporate responsibility, aiming to make a positive impact on communities worldwide.