Talent Recruitment

Responsibilities: 1. Preparation and training of product manufacturing process documents; 2. Selection and trial operation of production equipment, and formulation of production capacity standards for each process; 3. According to the requirements of the product fixture design and verification; 4. Deal with the corresponding NCMR in the production process, provide technical support for the production process and quality control; 5. Validation of the production process and product validation of the product; 6. Complete the tasks assigned by the superior leaders temporarily. Qualifications: 1. College degree or above, major in mechanical design, material molding or polymer materials; 2. At least 1 year process related working experience in medical industry or 3 years process experience in related industry; 3. Proficient in CAD, Office and other computer software; 4. Knowledge and experience in lean manufacturing, 5S, 6 sigma, etc; 5. Familiar with medical device laws and regulations, with quality management practice, ISO13485 quality system certification experience is preferred; 6. English reading and writing proficiency is better.

Responsibilities: 1. Responsible for the company's product planning (balloon catheter, stent, micro catheter, micro guide wire, accessories, etc.) and project planning, report to the R & D director; 2. According to the relevant laws and regulations and quality specifications of medical devices, as well as market and clinical needs, responsible for the design of new products, design verification, conversion and other related work of the entire development process; 3. Actively carry out technical research and technical improvement work, propose and implement feasible technical solutions and measures, and continuously improve product quality and process technology level; 4. Cooperate with other departments to complete product quality or regulatory registration and other related work. Qualifications: 1. Bachelor degree or above (including doctoral students), mechanical design, polymer, material engineering, biological engineering related majors; 2. More than 5 years of experience in the development of three types of interventional medical devices or engineering technology, familiar with the product development process and principles, familiar with the performance of engineering materials, applications and processing methods; 3. Proficient in engineering drawing software and MS office software; 4. Familiar with English information/literature query in the medical industry, with rich experience in project management, and the ability to analyze and solve organizational anomalies; 5. Strong learning ability, active work, self-driven, result-oriented;

Responsibilities: 1. Participate in product project evaluation, design new products and improve old products according to the requirements of design and development control procedures; 2. Responsible for the design of risk analysis and product realization of the whole process of risk management activities, the preparation of product risk analysis report and product risk management report; 3. Responsible for the preparation of design and development output documents (including product drawings, purchase details, product standards, instructions, etc.); 4. Responsible for product implementation planning and design conversion, to ensure that the newly developed products can be smoothly converted into listed products; 5. Responsible for product special process confirmation and reconfirmation; 6. Responsible for the determination of the technical parameters of the key process of the product, and participate in the organization of verification and re-verification; 7. Complete other tasks assigned by superior leaders. Qualifications: 1. Bachelor degree or above (including doctoral students), mechanical design, polymer, materials engineering, biological engineering related majors; 2. More than 5 years working experience in three types of medical device industry, with experience in balloon catheter, stent, guide wire and related accessories; 3. Familiar with production and quality management knowledge, good English, skilled use of office software; 4. Proficient in engineering drawing software, as well as data analysis software. Understand the six sigma quality management theory, project management and other basic knowledge; 5. Strong innovation ability, coordination ability and teamwork ability, good problem solving ability, learning ability and organizational ability.

Responsibilities: 1. Participate in the research and development of products in the field of cardiovascular intervention, including product material selection, structure design, performance research, etc. 2. Assist in the establishment of testing methods for new product performance research. 3, responsible for the research and development phase of the relevant supplier screening and material procurement. 4. Complete other tasks assigned by the leader. Qualifications: Bachelor degree or above (including doctoral degree), major in mechanical design, polymer, material engineering, biological engineering or related; More than 2 years working experience in three types of medical device industry, preferably with balloon catheter, stent, guide wire and related accessories; Proficient in engineering drawing software and data analysis software; Work conscientiously, have a sense of innovation, be able to actively complete the tasks in the project.

Responsibilities: According to the company issued the target task, according to the plan to complete the revenue task; Responsible for customer development, to complete the discovery of needs, customer tracking, business negotiations, contract signing process; Complete customer relationship maintenance and provide service support for customers. Qualifications: Bachelor degree or above, at least 1 year sales experience in Internet or operator, large high-tech product company; Familiar with product sales management systems and procedures; Quick thinking, strong sense of purpose, good strain and compressive ability.