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Job responsibilities:
1.Responsible for the research and development of viral vectors in cell therapy, including the production, concentration and purification of new viral vectors (lentivirus, adeno-associated virus, etc.) and non-viral vectors;
2.Responsible for the development of cell therapy products (CAR-T/ CAR-NK/TCR-T) and RNA/DNA drugs;
3.Responsible for the design of experimental schemes of R&D projects, coordinating team members to carry out relevant experiments, making statistical analysis of original experimental data, and writing R&D reports, report PPT, articles or patents;
4.Responsible for writing the national or provincial level scientific research/industrialization project task book, the development of project implementation plans, technical routes, mid-term/final assessment objectives and other core content;
5.Good communication and cooperation skills, high sense of responsibility and good professional ethics;
6.Responsible for training R&D scientists or R&D assistants to carry out relevant scientific experiments;
7.Complete other affairs assigned by superiors.

Job requirements:
1.Under 40 years old, master degree or above in biology, immunology, pharmacy, virology and other related majors, with 1-3 years or more research and development experience in cellular immune products/viral vectors/biomedical enterprises; Training or management experience in research institutes, universities or biomedical enterprises is preferred;
2.Pre-clinical R&D experience in CAR-T, CAR-NK, TCR-T cells and macrophages is preferred;
3.Experience in pre-clinical research and development of retroviral vector, lentiviral vector, adeno-associated virus vector, and non-viral vector is preferred;
4.Proficient in general inverted microscope, inverted fluorescence microscope, laser confocal microscope, q-PCR, flow detection and sorting, AKTA protein chromatography purification, digital PCR, enzyme marker, small animal imaging and other instruments preferred users;
5.Good communication and cooperation skills, high sense of responsibility and good work ethic;
6.Working hours: 5 days and 8 hours, two days off (if there is a need to work overtime for research and development tasks, you can adjust the rest or take a series of breaks)

Job responsibilities:
1.Assist the head of the Marketing Department to make and update relevant promotional materials, follow up key customers and promote order fulfillment;
2.Professional presentation skills: Good presentation logic and presentation skills, giving lectures in various academic conferences;
3.Clinical professional skills: understand the clinical professional knowledge of hematoma, solid tumor, etc., and master the clinical application of flow cytometry;
4.Responsible for maintaining the friendly and communication relationship between customers and potential customers on a daily basis, and providing pre-sales and after-sales services for customer projects through my professional knowledge;
5. Writing skills: can assist researchers to write and apply for academic and ethical materials for clinical research;
6.Formulation and fine-tuning of market strategies: analyze industry forms, gain insight into industry dynamics, and timely report the interpretation of market strategies to senior management according to industry dynamics;
7.Complete other tasks assigned by superiors.

Job requirements:
1.Under the age of 40, bachelor degree or above in biology, immunology, pharmacy, marketing and other related majors, with more than 3 years of work experience in cell immune product development, production and sales is preferred;
2. Technical marketing, CRA, CRC and other work experience is preferred;
3.Lead or participate in clinical research/clinical trial experience of cell therapy products is preferred, and have the experience and ability to visit hospitals and introduce clinical research; Or have the experience and ability to introduce and promote clinical research at academic conferences/conferences;
4.Good communication and cooperation skills, high sense of responsibility and good professional ethics;
5.Working hours: 5 days, 8 hours, weekends (if you have tasks that require you to work overtime, you can take alternate breaks or take consecutive breaks)

Job responsibilities:
1.Responsible for the daily quality inspection of immune cell therapy products (CAR-T, CAR-NK, etc.), including materials, intermediate products, finished products, environment, etc.
2.Responsible for the management and implementation of laboratory equipment, samples, reagents, media, strains, cells, standards, etc.
3.Participated in the preparation of quality inspection materials for IND or IIT clinical trials of cell therapy products.
4.Responsible for and participate in the verification work related to the company, and cooperate with the projects related to the company's strategic implementation laboratory, R&D testing and other work.
5.Participate in and execute equipment verification, analysis method development, verification and other work, including the preparation, review or implementation of verification schemes and reports.
6.Timely report anomalies, deviations and OOS in the laboratory, and cooperate with the investigation.
7.Participate in the preparation or review of quality system related management system documents.
8.Complete other affairs assigned by superiors.

Job requirements:
1.Under 45 years old, college degree or above in medicine, laboratory science, biology, immunology or pharmacy, with 2 years or more quality inspection experience in biomedical enterprises.
2.Must be familiar with qPCR method detection and qPCR method development experience, including: mycoplasma detection, CAR copy number detection, HCD detection, virus titer detection;
3. Experience in IND or IIT clinical application of cell therapy products is preferred;
4. Proficient in the use of a variety of quality inspection instruments is preferred, including q-PCR, flow cytometer, enzyme marker, etc.;
5.Understanding of cell therapy production quality management system related regulations and standards is preferred;
6. Work carefully and seriously, strong sense of responsibility, integrity, can deal with the common problems in the work;
7. Working hours: 5 days, 8 hours, weekends (if you have tasks that require you to work overtime, you can take alternate breaks or take consecutive breaks)

Job responsibilities:
1. Responsible for establishing and maintaining the document management system, drafting and revising departmental documents according to regulations.
2. Responsible for GMP document compliance review, issuance and withdrawal, archiving, electronic data backup, etc.
3. Responsible for the issuance of GMP system file numbers, file directories and record serial numbers.
4. Responsible for the daily connection with the technical department, organize and deal with the deviation and change in the production process and other quality management work.
5. Responsible for drafting communication letters, annual on-site audit plans, on-site audit programs and quality agreements.
6. Responsible for formulating self-inspection plans, assisting in GMP self-inspection, coordinating self-inspection resources, and tracking defects correction related to production
Implementation of positive preventive measures

Job requirements:
1. College degree or above in pharmacy, medicine and bioengineering, more than 3 years of working experience in cell and gene, pharmaceutical and bioengineering companies, with quality management experience. Understanding of cell therapy production quality management system related regulations and standards is preferred;
2.Organization and coordination ability, strong communication ability, rigorous, strong sense of responsibility, with a big picture and overall control ability; Work carefully, strong sense of responsibility, integrity, can deal with the common problems in the work;
3.Working hours: 5 days, 8 hours, weekends (if you have tasks that require you to work overtime, you can take alternate breaks or take consecutive breaks)