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QUALIFICATIONS / EXPERIENCE: ● BSc, MSc or PhD with relevant pharmaceutical research and development experience ● At least 3 years of industrial bioanalytical experience, ideally within pharma and biotech. GLP experience is a plus. ● Solid knowledge of LBA methods (PK/ADA). LC-MS experience in large molecule bioanalysis is a plus ● Strong hands-on abilities to independently develop bioanalytical solutions and troubleshoot ● Willingness to analyze bioanalytical samples in the timely fashion when needed. ● Basic knowledge of bioanalytical sample workflow for in-life studies. ● Familiar with the ADME and PK/PD experiments is a plus ● Proficient in English and comfortable working in a bilingual environment (English and Chinese, mainly in English) RESPONSIBILITIES / DUTIES: ● Independently manage the bioanalytical aspects of multiple assigned projects by providing end-to-end support to internal project teams and directing bioanalytical work at CROs for assay transfer and troubleshooting if needed. o Manage the development, transfer, qualification and technical leadership in issue resolution of specific and sensitive bioanalytical methods required for the discovery and development compound (drug), anti-drug antibodies (ADA) and soluble targets in the given project. o Manage and conduct the in-house sample analysis and deliver qualified data to internal stakeholders in a timely manner. o Participate in the laboratory operations such as matrix, reagents and consumable materials procurement and maintenance, etc. ● Support and co-develop PK/PD/ADA analytical strategies (e.g. technology, assays, matrices, sample collection) ● Improve and optimize laboratory workflows independently and creatively ● Ensure relevant compliance with the current global and local bioanalytical guidelines and GxPs.