Responsibilities:

(1) Responsible for pre-clinical research and development of novel parenteral drug injection platforms (microspheres, liposomes, injection suspensions, etc.) To serve as leader and mentor to guide formulation team in design and development of pharmaceutical products to meet the company's pharmaceutical development needs.

(2) Responsible for the project budgeting; project screening and selection; R&D process planning; organize and direct all required aspects of the R&D projects; Contribute drug regulatory filings; and project cost accounting.

(3) Constantly track industry dynamics, regularly appraise existing project, and maintain a high awareness and insight into unmet clinical needs market (such as brain-targeting drugs).

(4) Supervise and train formulation personnel.

(5) Resolve problems in formulation development and manufacturing process.

(6) Interact and collaborate with cross-functional teams throughout the drug product development process

(7) Responsible for project planning, technical guidance, quality audit, to ensure that the finished products are equivalent to the Reference Listed Drug (RLD) and can sufficiently achieve regulatory approval.

Qualifications:

(1) PhD in Pharmaceutical Sciences or Chemistry with 7-10 years of novel parenteral product development experience; or MSc in Pharmaceutical Sciences or Chemistry with 10-15 years of novel parenteral product development experience.

(2) Comprehensive knowledge and experience with full technical understanding and project management experience of pharmaceutical drug and traditional Chinese medicine.

(3) Familiar with the R&D process of novel parenteral products (microspheres, liposomes, injection suspensions, etc.), capable of independently conducting and presiding over drug development, proficient in the latest technological methods in the R&D field, aware of industry technology and business development trends. Have own unique insights of fundamental technology