Associate Scientist-lentiviral vector production

Major responsibilities : Execute activities related to manufacturing process transfer. Perform upstream production operations for lentiviral vectors and prepare associated production records and documentation. Establishment of cell banks for viral vector packaging. Routine maintenance of GMP production facilities. Manage the procurement and inventory of production materials. Assisting the PD team with relevant process development work as needed. Other tasks assigned by supervisors according to project requirements. Education, Qualifications, Skills and Experience Bachelor’s degree or above in pharmaceutical or biological sciences, or a related discipline. At least 2 years of hands-on GMP upstream production experience with viral vectors; familiar with GMP manufacturing workflows such as cleanroom gowning, material transfer, and room clearance procedures; strong awareness of aseptic operations. Candidates with process development experience for lentiviral vectors are preferred. Familiarity with lentiviral vector packaging processes and fundamental principles, such as traditional cell factory methods; experience with fixed-bed bioreactor platforms is preferred. Practical experience in scaled-up upstream production of lentiviral vectors and bioreactor cultivation. Excellent teamwork, resilience under pressure, and communication skills. Date Posted 18-8月-2026 Closing Date 30-8月-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.