1. Strategically design and guide the development of formulation and process of oral solid dosage forms;2. Provide hands-on operations for process scale up and technology transfer;3. Guide and participate in the GMP production of drug products for clinical trials;4. Manage collaboration with third-party companies;5. Drive strategic direction of amorphous solid dispersions, including hot melt extrusion and spray drying;6. Explore new formulation platforms, such as albumin, liposomes, etc;7. Draft technical reports and filing documents;

 Make project plans based on the requirements of ICH and FDA, monitor the project progress to ensure and be responsible for the delivery of the milestone;  Responsible for R&D of topical cream based on QbD concept, including intellectual property, preparation optimization, validation of detection method, PK/PD design and analysis, etc.; Manage ongoing communication and collaboration with third-party company; Have successfully finished lab-scale preparation of the product, and proved the effectiveness and feasibility in vivo, which is under technology transfer (scale up); Assist company in setting up new department; Responsible for IND-related work, and CMC documentations.

 Make project plans based on the requirements of ICH and FDA, monitor the project progress to ensure and be responsible for the delivery of milestone;  Responsible for R&D of parenteral injection, including intellectual property, preparation optimization, validation of detection method, PK/PD design and analysis, etc.; Manage ongoing communication and collaboration with third-party company; Have successfully finished lab-scale preparation of the product, and proved the effectiveness and feasibility in vivo, which is under technology transfer (scale up).

 Responsible for R&D of pegylated NGF in lab scale, including preparation, purification, characterization, etc.;  Make project plans based on requirements of ICH and CFDA; Have proved the effectiveness and feasibility in vivo.