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Salary
≈ $40k – $89k per year (Estimated)
Location
In office (Shanghai)
Seniority
Senior · 5+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 19, 2026. First seen by Alion on Oct 15, 2026. AstraZeneca scores A on the Alion truth index.

Overview
Company
Impact
Profile match
AstraZeneca is a British-Swedish pharmaceutical company formed in 1999 by the merger of Astra of Sweden and Zeneca of the United Kingdom, and now one of the largest drug makers in the world by revenue. Its portfolio is concentrated in oncology with Tagrisso, Imfinzi and Enhertu, alongside cardiovascular, renal and metabolic products including Farxiga, respiratory and immunology medicines, and a rare disease business built on the acquisition of Alexion. Headquartered in Cambridge in England and listed in London, Stockholm and New York, it reports in United States dollars.

Typical Accountabilities

  • Responsible for the screening, development, and optimization of formulations for Lentiviral Vector.
  • Responsible for designing and executing pharmaceutical formulation studies, including formulation screening and development, drug product process development, process characterization, primary packaging component selection and compatibility studies, and stability studies.
  • Responsible for authoring formulation development protocols and reports, and compilling supporting technical documentation for regulatory submissions.
  • Consolidate and present formulation development data and project learnings; establish development workflows; and build formulation process development capabilities within the team.
  • Partner with upstream and downstream process development, QC, and manufacturing teams to enable technology transfer and manufacturing scale-up.

Education, Qualifications, Skills and Experience

  • Master’s degree or higher in Pharmaceutics, Pharmacy, Bioengineering, Biopharmaceuticals, Cell Biology, or a related field.
  • 5+ years of experience in biologics formulation and process development; experience in LVV and AAV formulation development is preferred.
  • End-to-end experience in at least one relevant project covering formulation development, IND submission, and clinical supply manufacturing, together with demonstrated experience in preparing and compiling IND/NDA submission dossiers.
  • Strong knowledge of domestic and international regulatory requirements and formulation development guidelines, with demonstrated ability to independently lead project formulation activities and author IND/NDA submission dossiers.
  • Proficiency with DoE/statistical tools for study design and multivariate analysis (e.g., JMP, Design-Expert, Minitab).
  • Good command of written and spoken English, with the ability to search for and interpret international literature.
  • Strong teamwork and communication skills.

Date Posted

15-Oct-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.

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