1. Master’s degree or above in Clinical Medicine, Life Sciences, or related fields;

2. Minimum 3 years of relevant experience in pharmaceutical/biotech companies; experience in clinical work, data analysis, or literature review is a plus;

3. Familiar with domestic and international regulations, ICH, GCP, and other compliance standards;

4. Strong ability in literature research and analysis;

5. High sense of responsibility, good communication skills, and team spirit.

1. Bachelor’s degree or above in Medicine, Pharmacy, Life Sciences, or related fields;

2. Over 5 years of experience in clinical trial project management, with full-process management experience in Phase II clinical trials;

3. Familiar with regulatory requirements from FDA, NMPA, and others;

4. Strong communication skills, ability to handle multiple tasks, and conflict resolution skills;

5. Proficient in project management software (MS Project, Clarizen), EDC systems, and statistical analysis tools.

1. Ph.D. degree in Biomedical Sciences, Bioengineering, Biochemistry, or related fields. Experience in stem cell differentiation and development research is preferred;

2. Fluent in spoken English with strong writing skills in both English and Chinese;

3. Project and team management: Lead R&D projects independently, develop short- and long-term plans, assign tasks, continuously improve workflows, ensure timely project completion, communicate progress effectively, and manage and evaluate team members;

4. Development and innovation: Continuously conduct technical research, actively follow industry trends, overcome technical challenges, and propose innovative solutions;

5. Data and documentation management: Timely organize and summarize R&D data and documents, ensure proper archiving, and maintain data security and integrity;

6. Technical writing: Responsible for drafting and optimizing invention disclosures, academic papers, and project application materials to support intellectual property and technology transfer;

7. Assist other departments or positions with tasks as needed and complete other assigned duties.

1. Bachelor’s degree or above, with at least 3 years of experience in aseptic manufacturing management; experience in cell therapy and commercial-scale production is preferred;

2. Strong aseptic awareness, with solid knowledge of pharmaceutical regulations and GMP standards;

3. Experience in drafting production-related documents, including equipment qualification, aseptic process validation, and other GMP documentation;

4. Proven experience in team management. Responsible for equipment acceptance, commissioning, qualification, validation, and re-validation for production lines.