{"id":2606833,"url":"https://alion.io/job/astrazeneca-gene-vector-senior-scientist-ii","title":"Gene Vector Senior Scientist II","company":{"id":13195,"name":"AstraZeneca","domain":"astrazeneca.com","url":"https://alion.io/company/astra-zeneca","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":91,"open_postings":124,"ghost_share":0,"stale_share":0.508,"repost_share":0.056,"time_to_fill_p50_days":20,"computed_at":"2026-10-23T05:54:15Z"}},"role":"Science & Research","role_family":"Science & Research","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Shanghai, China"],"countries":["CN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":36000,"max_usd":81000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":1403},"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"JMP","optional":false},{"name":"Minitab","optional":false}],"status":"live","first_seen_at":"2026-10-15T09:58:26Z","employer_posted_date":"2026-10-15","last_verified_at":"2026-10-23T15:42:25Z","board_verified":true,"closed_at":null,"days_open":8,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":8},"description":"Typical Accountabilities\nResponsible for the screening, development, and optimization of formulations for Lentiviral Vector.\nResponsible 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.\nResponsible for authoring formulation development protocols and reports, and compilling supporting technical documentation for regulatory submissions.\nConsolidate and present formulation development data and project learnings; establish development workflows; and build formulation process development capabilities within the team.\nPartner with upstream and downstream process development, QC, and manufacturing teams to enable technology transfer and manufacturing scale-up.\nEducation, Qualifications, Skills and Experience\nMaster’s degree or higher in Pharmaceutics, Pharmacy, Bioengineering, Biopharmaceuticals, Cell Biology, or a related field.\n5+ years of experience in biologics formulation and process development; experience in LVV and AAV formulation development is preferred.\nEnd-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.\nStrong 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.\nProficiency with DoE/statistical tools for study design and multivariate analysis (e.g., JMP, Design-Expert, Minitab).\nGood command of written and spoken English, with the ability to search for and interpret international literature.\nStrong teamwork and communication skills.\nDate Posted\n15-Oct-2026Closing Date\n30-Dec-2026AstraZeneca 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. 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