R&D Assistants (In Recruitment)

Category: R&D

Release time: 2023 - 04 - 23

Position Responsibilities: 

1. Responsible for/cooperate with the research and development of molecular diagnostic IVD products;

2. Responsible for the specific development of molecular biology-related experiments and the management of corresponding reagent materials;

3. Responsible for the original records of the experimental process, collecting problems encountered in the development process and assisting with solutions;

4. Establish and complete all laboratory work in strict accordance with SOPs;

5. To complete other work tasks arranged by superiors. 


Position Requirements: 

1. Familiar with molecular biology experiments and principles, with sufficient practical or training basis in various types of PCR experiments;

2. Involved in nucleic acid isothermal amplification techniques (i.e. RPA, LAMP, etc.) or NGS database building is preferred;

3. Strong sense of responsibility, pragmatic and conscientious, with good execution;

4. Biotechnology, medical testing and other related majors, R&D assistant college degree or above;

5. Experience in IVD product development is preferred, excellent fresh graduates are also welcome to join.


Position Information

Working experience: 1-3 years

Education requirement: Bachelor

Clinical Project Assistants (In Recruitment)

Category: R&D

Release time: 2023 - 04 - 23

Position Responsibilities: 

1. Clinical interface: assist in the whole process of clinical trials according to the requirements of GCP and the company's project research plan; including communication and coordination with hospitals and patients, preparation, submission, daily management and updating of project documents, completion of the collection, organization, backup, filing and data entry of clinical trial project data, etc.;assist investigators in tracking subjects for regular follow-up visits, etc;

2. Registration declaration: assist in the whole registration process of medical devices; including assisting in the collation, submission and receipt of medical device registration data; assisting in the preparation of registration documents that comply with regulatory standards;

3. Assist in organizing the documentation output in the design and development process, and be responsible for departmental project affairs and internal and external communication;

4. Complete other work assigned by the supervisor. 


Position Requirements: 

1. Undergraduate degree or above, majoring in medicine, nursing, biology, pharmacy, medical equipment and other related majors;

2. Ability to communicate and coordinate well with people, good at handling interpersonal relationships;

3. Cheerful and lively personality, honest, reliable, realistic and stable;

4. Some clinical trial experience, able to accept short-term travel.


Position Information

Working experience: More than 1 year

Education requirement: Bachelor