1. Develop new products according to the R&D system;

2. Learn the company's R&D skills, optimize mature product processes and develop new product processes;

3. Cooperate with registered personnel to write product technical documents;

4. Cooperate with the inspection department to write and verify product inspection methods;

5. Assist the quality department in preparing product research and development and system documents;

6. Implement the process transformation from product research and development to production, and connect with production personnel to determine relevant technical parameters;

1. Have good English literature reading skills, master's degree is preferred, bachelor's degree or above is required;

2. Mechanical and polymer materials and other engineering majors, familiar with a 3D modeling software;

3. More than two years of R&D experience in the medical device industry;

4. Product developers who have worked on passive implants are preferred;

5. Familiar with the medical device product development process and ISO13485 quality system, and have priority in participating in animal experimental design or actual operation.

1. According to the company's design products, carry out 3D printing processing, and produce according to the process;

2. Communicate with the design engineer to understand the required structural functions and judge whether the design data meets the manufacturing requirements.

3. Process verification of the designed product (small batch trial production, process confirmation);

4. Responsible for the daily operation and abnormal disposal of the process module;

5. Responsible for the daily management, maintenance and upgrading of equipment and production lines to ensure process reliability;

6. Complete other tasks assigned by superiors;

1. Bachelor degree or above, with 3D printing, three types of passive implantable medical devices, absorbable material experience, and medical-industrial background is preferred;

2. Experience in SLA process and FDM process is preferred;

3. Proficient in 3D printing manufacturing software and auxiliary software (Magics, Cura, Python), data processing and analysis software (Excel or Origin), modeling software (UG or Solidworks);

4. Serious and pragmatic, responsible and teamwork;

5. Have strong self-learning ability and certain communication skills;

6. Take the initiative to explore potential defects and take necessary measures to avoid problems.

1. Lead the preparation and review of medical device product technical requirements, manuals and other registration and application materials;

2. Responsible for the innovation declaration, registration declaration, expert consultation meeting, registration and subsidy of Class II/III medical devices;

3. Participate in the verification of medical device production quality management system;

4. Pay attention to the relevant policies and information released on the websites of the National Medical Products Administration and the Provincial Drug Administration, and keep abreast of the relevant policies and latest developments in medical device registration.

5. Responsible for the withdrawal of medical device registration applications and other work related to medical device registration applications;

6. Participate in the review of medical device preclinical trials and clinical trial plans, and connect with the relevant work of clinical trials;

1. Bachelor degree or above, medical device-related major is preferred;

2. More than 3 years of work experience related to medical device registration;

3. The number of medical devices participating in the declaration of Class III is not less than 3;

4. Familiar with the laws, regulations, rules and relevant regulations of medical device registration and filing management;

5. Have good organization, communication and coordination skills;

6. Have strong learning ability and be able to keep abreast of the latest developments of medical device registration policies and products.