Role at a glance
- Job function
-
Engineering & R&D Biotechnology & Pharmaceutical R&D
- Salary
- Not Disclosed
- Location
- Shanghai, Guilin Road
- Employment
- Full-time
- Experience
- Senior Level 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.
- Education
- Master’s degree or higher in Pharmaceutics, Pharmacy, Bioengineering, Biopharmaceuticals, Cell Biology, or a related field.
Spotted an issue?
We’ll check it against the original posting.
Role Summary
The Gene Vector Senior Scientist II develops and optimizes lentiviral vector formulations and pharmaceutical formulation processes. The role supports formulation studies, technical documentation, and manufacturing scale-up and technology transfer.
What You'll Do
- Screen, develop, and optimize lentiviral vector formulations.
- Design and execute formulation screening and development, drug product process development, process characterization, packaging...
- Author formulation development protocols and reports, and compile technical documentation for regulatory submissions.
- Consolidate and present formulation development data and project learnings, establish development workflows, and build formulation...
- Partner with upstream and downstream process development, QC, and manufacturing teams to support technology transfer and manufacturing...
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
Requires a Master’s degree or higher in a listed or related field, at least 5 years of biologics formulation and process development experience, relevant end-to-end project and IND/NDA dossier experience, regulatory knowledge, DoE/statistical tool proficiency, English proficiency, and teamwork and communication skills.
Required
- 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.
- End-to-end experience in at least one relevant project covering formulation development, IND submission, and clinical supply...
- Strong knowledge of domestic and international regulatory requirements and formulation development guidelines, with demonstrated ability...
- 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.
Preferred
- Experience in LVV and AAV formulation development is preferred.
Original job description
Content provided by the employer
Original job description
Content provided by the employer
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-2026Closing Date
30-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. 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.
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.