
MSAT Scientist
- CAPA
- GMP
Not enough detail in this posting to match
Major responsibilities
- Engage in tech transfer business, such as preparation of TTP, gap analysis, knowledge transfer and training, to proceed the project as schedule.
- Ensure the integrity of tech data and documentations, and timely update as required.
- Conduct the process related investigation, optimization and scale-up study.
- Handle the tech related troubleshooting, deviations, change and CAPA during manufacture business.
- Participate in the related validation studies, including chromatography resin, reusable filter member lifetime validation, mixing study, cleaning study and yield study et al.
- Attend in GMP audits, regulatory filing as required.
Education, Qualifications, Skills and Experience
- Master’s degree or above on biological or pharmaceutical relevant major. Graduates from 211/985 Project universities and those with overseaswork experience are preferred.
- More than 3 years’ experiencein MSAT or processdevelopment, with the experience of BLA or cell and gene therapy industry preferred.
- Be familiarwith QbD, GMP and other related regulations/guidance.
- Good statistical analysis capacity.
- Goodwritten English and fluent oral English.
Date Posted
15-Sept-2026Closing Date
30-Dec-2026AstraZeneca embraces diversity and equality of opportunity. Â 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. Â We believe that the more inclusive we are, the better our work will be. Â We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. Â 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.
MSAT Scientist · AstraZeneca Pharmaceuticals LP Company