Responsibilities:

1. Responsible for developing new medical device , including  planning, input, output, verification and transformation of new products;

2. Assist the project manager to coordinate relationships among developments of manufacturing, quality and procurement  according to the assigned plans and tasks of new  project ,and promote  the  r&d projects going smoothly;

3. Responsible for new product BOM, raw material, semi-manufacured  and manufactured products standard, production operation procedures, parts and assembly drawings and other technical documents;

4. Responsible for selecting material suppliers and confirming material conformity;

5. Mold processing and equipment selection;

6. Responsible for the implementation of new product process verification, preparation of the scheme, and organize relevant personnel to implement, and finally determine the product process;

7. Responsible for new product transfer training,  production education, quality and procurement related personnels, so that mass production can meet the established requirements;

8. Other tasks assigned by superior leaders.

Requirements:

1. Major in mechanical design, material science, medical equipment, etc.;

2. Experience in developing intravenous infusion products, such as PORT, PICC and other products;

3. Familiar with solidWord, PROE and other 3D and 2D design software;

4. Proffessional in  quality management standards of sterile medical devices, and be familiar with the design and development process of medical devices.

Working Experience:

At least 3- year experience in medical device design or technical position.

Comprehensive Ability: 

Strong sense of responsibility, communication and coordination ability, analysing ,problem-solving and team work ability.

Well paid,  benefits negotiable for top tallents.