1. Responsible for the development of the purification process of nucleic acid drug molecules.

2. Chromatography technology selected by molecular characteristics and scaled up accordingly.

3. Use analytical chemistry technology to develop quality inspection methods.

4. Complete the corresponding technical documentation.

1. Biology, chemistry, pharmacy and other related majors, master degree or above.

2. More than one year of working experience in related companies, RNA and DNA purification experience is preferred.

3. Experience in a variety of chromatographic purification techniques, and experience in production scale-up is preferred.

4. Able to read English technical documents proficiently.

1. Responsible for the technical research and development of mRNA product formulations, responsible for screening and optimizing formulations and process parameters

2. Responsible for formulating and adjusting the experimental plan for preparation development, collecting experimental reports and sorting out experimental data;

3. Responsible for investigating and tracking domestic and foreign industry trends, participating in the investigation and summary of project or technical platform related documents, as well as the collation and writing of research reports;

4. Participate in technical research in project development, solve technical problems encountered in the project, and write and declare related technical patent materials;

1. Master degree or above in chemistry, materials, pharmacy, biology or related majors. Experience in the research and development of mRNA-related preparations is preferred, and recent graduates with experience in the research and development of nano-pharmaceutical preparations are also available

2. Able to solve technical problems encountered in experiments and implement solutions through investigations. Collect and analyze the data in the research and development process, and be able to make comprehensive judgments and make further suggestions

3. Comprehensively master the various operations of the laboratory, have good operational capabilities in certain fields, and can guide other employees in the technical work

1. Responsible for the construction of the enterprise preparation technology platform

2. Manage mRNA product formulation and process development, production and GMP pre-clinical preparation production

3. Responsible for screening and optimizing formulations and process parameters, and participating in related patent drafting

4. Establish and optimize the quality characteristics detection system of mRNA preparations, and participate in the writing of relevant documents

5. Responsible for formulating and implementing related SOPs of the preparation department and completing relevant personnel training

1. Master degree or above in chemistry, materials, pharmacy, biology or related majors. Experience in the development of mRNA-related preparations is preferred

2. More than one year of doctoral work experience, and more than three years of master's work experience

3. Familiar with injectable preparations GMP, GLP domestic and foreign relevant laws and regulations, technology, operation process and application requirements are preferred

4. Have leadership skills, excellent communication skills in Chinese and English, and a sense of responsibility

1. Responsible for the prediction and screening of drug targets, drug structures, antigen epitopes, etc.;

2. Use a variety of bioinformatics software and statistical methods to mine transcriptome data;

3. Lead the development and application of biological information standardization methods;

4. Cooperate with the smart laboratory team for process development;

5. Responsible for building a bioinformatics team, participating in internal training and external cooperation;

6. Have a master's degree or above in bioinformatics, computational biology or related fields;

7. Experience in immunology or structural biology is preferred;

8. Those who understand cancer, gene silencing, enzyme engineering, epitope screening or clinical data analysis are preferred;

9. Proficiency in reading relevant literature and tracking industry development trends;

1. Responsible for the establishment, operation and continuous improvement of the company's quality system;

2. Responsible for R&D and production quality management system planning and management (GLP), phased and final review of relevant documents, supervision, inspection and review during the implementation process;

3. Responsible for on-site management of R&D and production, supervision of on-site process implementation and GMP implementation;

4. Responsible for the quality supervision and release of the company's products;

5. Responsible for organizing various GMP and non-GMP inspections and audits at home and abroad;

6. Responsible for the management and training of the team.

1. More than 5 years of QA work experience. Bachelor degree or above in clinical, pharmacology or biomedical related fields is preferred;

2. Familiar with the drug development process, relevant laws, regulations and policies;

3. Have the ability to solve problems and coordinate complex compliance issues;

4. Have strong inter-departmental communication skills and interpersonal skills;

Bachelor degree or above; 10-30k; flexible working hours; employee travel; paid annual leave; regular physical examination; large room for development;

1. Responsible for the upstream research and development, screening and production of protein products.

2. Responsible for downstream pilot scale up, production process development and technology transfer, batch records, SOP and other pilot production documents review and revision

3. Use analytical chemistry technology to develop quality inspection methods.

4. Complete the corresponding technical documentation.

1. Major in molecular biology, fermentation, etc., bachelor degree or above. Proficiency in reading and writing technical documents in Chinese and English.

2. More than 2 years of working experience in related companies.

3. Experience in a variety of chromatographic purification techniques, and experience in production scale-up is preferred.