Research Interests: 

Research in molecular diagnostics, companion diagnostics, immunol testing and screening of novel markers, rapid diagnostics (POCT), etc. 

Position Responsibilities: 

1. Track and understand the development of international antibody diagnostic technology in a timely manner;

2. Focus on the current situation of disease development and treatment level in the involved fields, pay attention to the frontier and progress, research and analysis of industry trends. 

Position Requirements: 

1. Candidates with doctoral degree in recent years in China or other countries，under 40;

2. Experience in molecular biology, immunology, biochemistry, cell biology, bioinformatics, etc;

3. Strong sense of responsibility, and the ability to lead scientific research and development projects;

4. Experience in R&D of in vitro diagnostic reagents is preferred but not essential;

5. Excellent analytical, organizational and communication skills; good oral, written and communication skills in English and Chinese; excellent teamwork skills.

Research Interests: 

Antibody product preparation, detection and evaluation; molecular cloning, protein expression and purification; biochemistry and molecular biology, etc. 

Position Responsibilities: 

1. Develop/optimize R&D protocols, complete R&D tasks on time and as required, and solve problems arising during R&D;

2. Implement laboratory specifications, complete experimental operations, data analysis and processing, report writing. 

3. Drafting and writing of project related design and development documents. 

Position Requirements: 

1. Master's degree or above, majoring in biochemistry, molecular biology, immunology, cell biology, medical testing and other

related majors, fresh graduates are also eligible;

2. With solid theoretical and practical experience in cell biology, molecular biology or antibody, more than three years of work experience in undergraduate;

3. Skilled in cell culture, ELISA, WB, Flow and other detection techniques, according to the subject requirements to complete

experiments independently;

4. Strong independence, practical and dedicated work, rich in responsibility and teamwork spirit.

Position Responsibilities: 

1. Responsible for new product registration, registration certificate changes and re-registration of expired registration;

2. Responsible for the collection, transformation and training of medical device product standards and other related standards in the medical device industry;

3. Responsible for the implementation of medical device laws and regulations, timely understanding of the dynamics of medical device laws and regulations, and timely access to newly released and newly revised laws and regulations;

4. Responsible for the management of departmental files, information and literature;

5. Responsible for medical device production, business enterprise laws and regulations, medical device product registration process and the preparation of product registration information, and declaration. 

Position Requirements: 

1. Bachelor degree or above in biology, medicine, pharmacy related majors;

2. More than 3 years of relevant work experience in the medical device industry;

3. Familiar with the relevant policies and regulations and quality standards of the national medical device industry.

Position Responsibilities: 

1. Responsible for planning and managing the projects and tasks related to the international registration of the company's products;

2. Responsible for other qualifications and documents for product access to international markets;

3. Collect and organize the registration requirements of each country, familiar with the registration laws and regulations of each country;

4. The whole process of tracking the progress of the international registration of products, at any time to deal with problem solving;

5. Complete other work arranged by the leadership. 

Position Requirements: 

1. Medicine, pharmacy, laboratory science, biology and other related majors, bachelor degree or above, English level 6 or above, proficient in listening, reading and writing;

2. Have more than 3 years of in vitro diagnostic reagent product registration work experience; 1 year or more of international registration work experience in medical devices;

3. Some experience in in vitro diagnostic reagent quality management system.