PI (Biomedicine, AI, Stem Cells, IVD, Tissue Engineering, etc.)
1.Independently lead a research team to conduct innovative scientific research aligned with the institute’s strategic goals and development plans.
2.Apply for scientific research grants and funding independently.
3.Manage and guide the research team’s scientific activities.
4.Actively participate in institute-related activities, including academic conferences, student recruitment, talent hiring, and collaborative exchanges.
Compensation & Benefits:
1.Internationally competitive salary package.
2.Ample start-up funding, research space, and office facilities based on project needs.
3.Access to cutting-edge technology platforms.
4.Support for building a dedicated research team, including PhD students, postdocs, and full-time researchers.
5.A collaborative, interdisciplinary, and frontier-focused academic environment.
6.Dedicated support for applying for research grants and awards at all levels.
7.Professional team and incubation platform to facilitate technology transfer and commercialization.
8.Assistance for foreign employees with work permits, residence permits, and tax incentives.
9.Comprehensive benefits, including social insurance, supplementary medical insurance, annual health check-ups, and paid leave.
Office Director
1.Bachelor’s degree or higher, preferably in Chinese, Public Administration, Public Affairs, Journalism, Medicine, or related fields.
2.Extensive experience and established connections in liaising with central and local government departments.
3.Prior work experience in government agencies is preferred, with familiarity of governmental structures and core workflows.
4.Excellent interpersonal and coordination skills, strong teamwork mindset, and solid public affairs management capabilities.
5.Adaptability to complex or challenging environments, with high resilience and problem-solving skills.
6.Detail-oriented, responsible, proactive, and eager to learn.
7.Exceptional official document drafting and report-writing abilities, with clear logic and standardized expression.
1.Responsible for drafting and standardizing various documents, including press releases, reports, official correspondence, and administrative paperwork, with strong writing skills and professional expression.
2.Efficiently and accurately receive, interpret, and process external documents (e.g., government notices, partner communications), ensuring timely responses, compliant replies, and proper implementation of requirements.
3.With at least 3 years of administrative management experience, effectively coordinate workflows, resources, and cross-departmental collaboration to ensure accurate, timely, and efficient internal and external dissemination and execution of policies, decisions, and information.
4.Manage communication and relationship-building with government agencies, media outlets, and other external organizations.
5.Participate in planning and executing public relations initiatives to enhance the institution’s public image and influence.
6.Stay updated on policies related to biotech, healthcare, medicine, anti-aging, translational medicine, and R&D industries. Analyze policy trends to identify opportunities and compliance risks, providing forward-looking and actionable recommendations aligned with institutional goals.
7.Complete other tasks assigned by leadership.
Project Leader - Cardiac Progenitor Cell
1. PhD in Pharmacy, Life Sciences, Cell Biology, Molecular Biology, or related fields.
2. Candidates with experience in pluripotent stem cell induction and differentiation are preferred.
3. Strong sense of responsibility, excellent communication skills, and teamwork spirit.
4. If available, please attach PDF files presenting professional capabilities.
1. Conduct independent research on cardiac progenitor cells under the guidance of the Principal Investigator (PI).
2. Independently apply for grants and projects.
Project Leader – Organoid
1. PhD in Pharmacy, Life Sciences, Cell Biology, Molecular Biology, or related fields.
2. Candidates with prior experience in organoid are preferred.
3. Strong sense of responsibility, excellent communication skills, and teamwork spirit.
4. If available, please attach PDF files presenting professional capabilities.
1. Conduct independent research on organoids under the guidance of the Principal Investigator (PI).
2. Independently apply for grants and projects.
Project Leader - Immunotherapy
1. PhD in Immunology, Pharmacy, Life Sciences, Cell Biology, Molecular Biology, or related fields. Candidates with a PhD degree in Immunology will be given priority.
2. Candidates with prior experience in tumor immunotherapy, immune-senescence (aging-related immunology), or autoimmune disease research are preferred.
3. Being able to independently conduct and apply for research projects.
4. Strong sense of responsibility, excellent communication skills, and teamwork spirit.
5. If available, please attach PDF files presenting professional capabilities.
1. Conduct independent research on cardiac progenitor cells under the guidance of the Principal Investigator (PI).
2. Independently or collaboratively apply for grants and projects.
Research Assistant - Cardiac Progenitor Cell
1. Master's degree in Pharmacy, Life Sciences, Cell Biology, Molecular Biology, or related fields.
2. Candidates with experience in pluripotent stem cell induction and differentiation are preferred.
3. Strong sense of responsibility, excellent communication skills, and teamwork spirit.
4. If available, please attach PDF files presenting professional capabilities.
1. Conduct independent research on cardiac progenitor cells under the guidance of the Principal Investigator (PI).
2. Assist in applying for grants and projects.
Research Assistant - Drug Discovery
1. Bachelor's degree or higher in medical-related fields (Master's degree preferred).
2. Candidates with prior experience with animal studies are preferred.
3. Strong sense of responsibility, excellent communication skills, and teamwork spirit.
4. If available, please attach PDF files presenting professional capabilities.
1. Conduct independent research on drug discovery under the supervision of PI.
2. Assist in applying for grants and projects.
Research Assistant - Organoid Research
1. Master's degree in Pharmacy, Life Sciences, Cell Biology, Molecular Biology, or related fields.
2. Candidates with prior experience with organoid are preferred.
3. Strong sense of responsibility, excellent communication skills, and teamwork spirit.
4. If available, please attach PDF files presenting professional capabilities.
1. Conduct independent research on cardiac progenitor cells under the guidance of the Principal Investigator (PI).
2. Assist in applying for grants and projects.
Research Assistant - Anti-Aging Research
1. Master's degree or above in Synthetic Biology, Pharmacy, Life Sciences, Cell Biology, Molecular Biology or related fields.
2. Candidates with prior experience with synthetic biology are preferred.
3. Proficient in English reading and writing.
4. Strong communication skills.
5. Strong sense of responsibility, excellent communication skills, and teamwork spirit.
6. If available, please attach PDF files presenting professional capabilities.
1. Execute research tasks assigned by PI.
2. Collaborate with lab researchers to complete scientific projects.
3. Perform routine server management and maintenance.
Research Assistant - Immunology
1. Bachelor's degree or higher in Immunology, Pharmacy, Life Sciences, Cell Biology, Molecular Biology or related fields (Immunology degree preferred).
2. Candidates with prior experience with immunotherapy are preferred.
3. Proficient in English (reading/writing).
4. Strong communication and interpersonal skills.
5. Strong sense of responsibility with excellent communication and teamwork skills.
6. If available, please attach PDF files presenting professional capabilities.
1. Execute immunology research tasks assigned by PI.
2. Collaborate with lab researchers to complete scientific projects.
3. Perform routine server management and maintenance.
Medical Specialist
1. Master's degree in Basic Medicine, Epidemiology, Public Health, Pharmacy, Life Sciences or related clinical medicine fields.
2. Excellent English proficiency (reading/writing); Strong writing skills (experience in drafting medical conference press releases preferred).
3. Excellent communication skills.
4. Proficient in medical literature databases and English medical literature review.
5. Strong sense of responsibility, excellent communication skills, and teamwork spirit.
1. Conduct industry and project research.
2. Track cutting-edge medical information and perform literature reviews.
3. Collect, analyze and organize product information and medical literature.
Medical Device Registration
1.Bachelor’s degree or higher, preferably in medical devices, biomedical engineering, or related fields.
2.Minimum 3 years of hands-on experience in end-to-end medical device registration, with at least 3 independently led Class III medical device registration projects (including innovative channel applications).
3.In-depth knowledge of NMPA and provincial registration regulations, with proven ability to manage documentation, supplement responses, expert consultations, and other critical registration stages.
4.Experience collaborating with CROs, with the ability to oversee quality and timelines for outsourced clinical trials, testing, and verification processes.
5.Strong communication and coordination skills with regulatory agencies, familiarity with priority review policies, and special approval pathways for innovative medical devices.
6.Fast learner capable of adapting to regulatory changes (e.g., Marketing Authorization Holder (MAH) system, AI medical device evaluation guidelines) and implementing compliant practices.
1.Lead the preparation and review of registration documents such as product technical requirements and instructions for use, oversee the entire registration process, and ensure compliance and timeliness.
2.Manage NMPA Class III medical device innovation applications, registration submissions, expert consultation meetings, and registration supplement responses, and coordinate with CROs (Contract Research Organizations) for clinical trial protocol design, data organization, and submission data alignment.
3.Participate in medical device quality management system audits, assist regulatory authorities in on-site inspections and follow-up on corrective actions to ensure seamless integration between registration and production processes.
4.Monitor policy updates from the National Medical Products Administration (NMPA) and provincial regulatory agencies, adjust registration strategies accordingly, and oversee full-cycle management including application withdrawal and resubmission.
5.Review pre-clinical and clinical trial protocols, lead collaboration with CROs and medical institutions, and ensure trial data meets registration evaluation requirements.
6.Establish efficient communication channels with regulatory bodies (e.g., NMPA, Center for Medical Device Evaluation), track review progress, and resolve technical issues to enhance registration success rates.
7.Other tasks assigned by leadership.
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