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1. Responsible for SEC, IEC, CE method development, validation, transfer and sample analysis of therapeutic antibodies.
2. Hands-on scientific expertise and problem-solving skills in CE or HPLC analysis.
3. Co-ordinate with project teams to streamline the sample testing.
4. Performs instrumentation routine maintenance.
5. Fully document all protocols and results in notebook and compose summary report.
6. Write formal reports for regulatory filings and support the generation of appropriate responses to questions from regulatory authorities.
7. Additional responsibilities may include other physicochemical test of samples.

1. PhD or MS 3+ years of experience in protein biochemistry, analytical chemistry, structural biology, immunobiology, pharmaceutical science or other related disciplines.
2. Comprehensive knowledge of HPLC and capillary electrophoresis, or other protein biochemistry techniques. Experience of working with therapeutic antibodies IND/BLA filing is a plus.
3. Ability to implement state of the art technologies to solve complex analyitical problems.
4. Strong capabilities in experimental design and execution.
5. Exceptional communication skills and the ability to work in a cross-functional team environment to advance CMC development projects. Fluent in English is a plus.

Working location: Nanjing