R&D Scientist

1. Responsible for the analysis of public databases or sequencing and chip data;

2. Responsible for the research and development of new data analysis and mining methods, platform construction and maintenance;

3. Design and evaluate detection algorithms for different test samples and different mutation types, and evaluate the quality of bioinformatics analysis;

4. Responsible for the development and maintenance of internal databases.

1. Master degree or above, major in bioinformatics, molecular biology, applied mathematics, statistics or other related majors;

2. Familiar with high-throughput sequencing principles and related applications, those with experience in high-throughput omics data processing and analysis are preferred;

3. Have a strong background in probability theory and mathematical statistics, and be proficient in various statistics and data analysis algorithms;

4. Familiar with Linux system, have independent programming ability, and be proficient in at least one programming language (Perl, R, Python, C/C++, Java);

5. Have good Chinese and English reading and writing skills;

6. Those who are familiar with common bioinformatics knowledge and related databases and bioinformatics analysis software are preferred.

1. Responsible for the application of hospital project cooperation funds, follow-up of various projects, and complete project reports in stages;

2. Responsible for the technical support of scientific research projects, and undertake related experiments (depending on the specific content of the project), such as quantitative and qualitative PCR, miRNA, western-blot, ELISA, methylation, ctDNA detection and other experiments, and analyze experimental data and write project reports;

3. Responsible for the collation, analysis and archiving of experimental data of all projects applied for in cooperation with hospital projects.

1. Doctor of Medicine degree, with molecular biology knowledge and experience related to medicine, and those with experience in applying for funds are preferred;

2. Have strong ability to analyze and solve problems, and be good at learning new skills;

3. English proficiency requires proficiency in reading and correctly understanding English literature;

4. Cheerful personality, rigorous work style, strong sense of responsibility, good execution, dedicated work attitude and good teamwork spirit.

1. Responsible for or assist in the research and development of in vitro diagnostic reagents;

2. Responsible for various experiments: quantitative and qualitative PCR, miRNA, western-blot, ELISA, methylation, ctDNA detection, etc., record experimental data, and write research and development reports;

3. Responsible for the preparation and organization of data in the reagent research and development stage;

4. Responsible for the daily maintenance and management of laboratory-related instruments and equipment.

1. Master degree or above in biology, immunology, pharmaceuticals, medical testing and other related majors;

2. Strong laboratory operation technical ability and research and development spirit (steadfast, dedicated and diligent);

3. Honest, humble, have certain communication skills and strong teamwork spirit. (Master graduates who are interested in experiments are welcome)

1. Responsible for the technical operation of scientific research projects, quantitative PCR, miRNA, western-blot, ELISA, methylation, ctDNA and other detection experiments, and analyze experimental data and write project reports;

2. Responsible for the collation and analysis of experimental data of technical service projects and the archiving of related materials.

3. Responsible for testing and processing biological samples, analyzing experimental results, collating data and feedback information;

4. Participate in the optimization of experimental processes, including the formulation of experimental plans and the collation and analysis of experimental data;

5. Responsible for the daily maintenance and maintenance of related instruments, and record the use and maintenance of instruments.

1. College degree or above in medical testing and biotechnology related majors;

2. Possess a solid theoretical foundation in cell biology, master cell biology related experimental skills, and have a foundation in tumor cell biology;

3. English level CET-4 or above, with basic English reading ability.

4. Careful and cautious work, strong sense of responsibility, good team spirit, and love laboratory technical work

1. Organize the formulation of quality management system documents and guide the implementation of the documents;

2. Supervise relevant departments and post personnel to implement the laws, regulations and norms of the medical industry involved in the company's business;

3. Responsible for the review of the legality of the supplier and the purchaser, the legality of the purchased products, and the sales staff of the supplier and the purchasing staff of the purchaser, and conduct dynamic management according to the changes in the review content;

4. Responsible for the collection and management of product quality information and the establishment of quality files;

5. Responsible for the acceptance of products, guide and supervise the quality management of procurement, storage, maintenance, sales, returns, transportation and other links;

6. Responsible for the confirmation of unqualified products and supervise the handling process of unqualified products;

7. Responsible for the investigation, handling and reporting of quality complaints and quality accidents ;

8. Responsible for product quality inquiry, reporting of fake and inferior products, and management of product recalls;

9. Organize internal audits and risk assessments of the quality management system;

10. Organize inspections and evaluations of the quality management system and service quality of in vitro diagnostic reagent suppliers and purchasers;

11. Organize reviews of the transportation conditions and quality assurance capabilities of the carriers entrusted with transportation;

12. Assist in quality management education and training;

1. Full-time undergraduate degree or above, majoring in biotechnology, medicine or medicine;

2. More than 4 years of experience in the pharmaceutical, medical laboratory or in vitro diagnostic reagent industry, familiar with related verification work management;

3. Familiar with ISO9001, ISO13485 and other quality management systems;

4. Meticulous and down-to-earth work, clear thinking, organized, responsible, strong writing skills and communication and coordination skills;