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AstraZeneca

Gene Vector Senior Scientist II

AstraZeneca is hiring a Gene Vector Senior Scientist II in Shanghai, China. Level rates it ; you can apply on Level.

Level's read on this job

  • Little AI ●○○○ is how Level rates this role: aI is not part of the work.
  • The posting mentions Jmp, Design Expert and Minitab among its tools and skills.
  • Level classes it as a senior role.
  • AstraZeneca has 1,100+ other open roles on Level.
  • This posting went up in the last few days.

AI in this role

Design and execute pharmaceutical formulation and process development studies for viral vectors while authoring regulatory submission dossiers.

jmpdesign-expertminitab
formulation-developmentbiologicsregulatory-submissionsdoestatistical-analysis

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.

How we rate this

Gene Vector Senior Scientist II at AstraZeneca rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Formulation DevelopmentBiologicsRegulatory SubmissionsDoeStatistical AnalysisJmpDesign ExpertMinitab

Questions you could be asked

  1. Tell me about a project where formulation development was part of your work. What did you do?
  2. Tell me about a project where biologics was part of your work. What did you do?
  3. Tell me about a project where regulatory submissions was part of your work. What did you do?
  4. Tell me about a project where doe was part of your work. What did you do?
  5. Tell me about a project where statistical analysis was part of your work. What did you do?

Adapt your resume

  • List these exact terms on your resume: Formulation Development, Biologics, Regulatory Submissions, Doe, and Statistical Analysis. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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