Job responsibilities:

be fully responsible for the market development and sales of the company's whole product line (RF therapeutic instrument, RF electrode needle, etc.), and be responsible for the training of team members and team construction;

Job requirements:

previous annual performance above 5000W is preferred; Team management ability; The resources of oncology department, hepatobiliary department, extrathoracic department and intervention department in class III first-class hospital are preferred; Dealer resources are preferred;

Salary:

open talk

Job responsibilities:

1. Improvement of inspection efficiency and qualification rate;

2. Be responsible for the inspection of raw materials, process products and finished products;

3. assist in production and verification;

4. Complete other tasks assigned by the Department Manager.

Job requirements:

1. Junior high school degree or above, with clear handwriting;

2. Universal caliper, vernier, etc;

3. Be able to read simple drawings;

4.Working experience in clean workshop is preferred.

Job responsibilities:

(1) assist to complete the quality objectives according to the annual quality objectives formulated by the company: ensure the compliance of production environment, water system and other relevant conditions, and assist to complete the annual quality objectives of inspection.

(2) Ensure the conformity of production related links:
 ① Control and daily monitor the company's production environment, process water and process gas;
 ② Conduct initial contamination bacteria and sterility test for products and issue corresponding reports;
 ③ Assist in the verification and detection of microorganisms related to production products;
 ④ Implement the annual verification of equipment and methods of the quality department.

(3) The sorting and analysis of test data provides management basis for quality management decision-making:
 ① Analyze microbiological and other related inspection data, monitor the microbiological level of the company and provide basis for quality management decision-making;
 ② According to the trend analysis of data, put forward the scheme to solve the trend deviation and assist in rectification.

(4) Maintenance of inspection environment and improvement of inspection methods:
 ① Control and daily monitor the company's production environment, process water and process gas;
 ② Ensure the sanitation of class 100 clean inspection room;
 ③ Assist in the rectification of existing inspection equipment and methods to improve the effectiveness and efficiency of inspection.

(5) Complete other tasks assigned by the superior.

Job requirements:

1. Major in biochemistry or relevant training, technical secondary school or above;

2. Be familiar with relevant biochemical detection methods and operations;

3. Be familiar with the environmental requirements for medical device manufacturers.

Job responsibilities:

1. Be responsible for business development and product promotion in Central China (Hubei, Jiangxi, Yunnan, Guizhou, Sichuan and Chongqing), and ensure the communication of information among agents, clinics and companies;

2. Do a good job in channel management in Central China, organize agents to participate in various academic conferences in the region, and do a good job in agent training;

3. Maintenance and management of KOL customers in the region.

Job requirements:

1.5 years of relevant working experience in medical industry, medical related major is preferred;

2. Have received training in marketing and product knowledge, and be familiar with marketing;

3. have professional spirit and enthusiasm, and can bear strong work pressure;

4. Have the ability to analyze and solve problems independently;

5. Have good teamwork spirit and professionalism, good communication skills and persuasion.

Job responsibilities:

1. Sorting of procurement contract qualification;

2. Registration of purchase invoices, sorting and statistics of logistics receipt;

3. Develop and manage channel suppliers and maintain their relationship;

4. Other procurement work assigned by the leader.

Job requirements:

1. Fresh graduates in 2021 majoring in medical devices, pharmacy and medicine;

2. Have certain English conversation ability;

3. Familiar with office software;

4. Honest and trustworthy, serious and meticulous work, thoughtful and enthusiastic service;

5. Loyal to the enterprise, abide by the company's rules and regulations, have good learning and enterprising spirit and team spirit;

Job responsibilities:

1. Earnestly implement the company's sales management regulations and implementation rules, and strive to improve their own business level;

2. Actively achieve the sales targets specified in the region and provide satisfactory services to customers;

3. Implement and assist after-sales service, timely understand the weekly and monthly usage and inventory of the hospital, manage and track the agents, and ensure the timely performance of the contract;

4. Understand customer needs and grasp market information in time;

5. Establish good cooperation with customers, ensure effective communication, deal with customers' opinions and complaints in time, and enhance customer satisfaction;

6. Collect marketing information and market feedback information to provide basis for the company's marketing planning and product improvement.

Job requirements:

1. At least 1 year sales or marketing related experience, college degree or above, medical related major is preferred;

2. Enthusiastic, good attitude, hard-working;

3. Good team work spirit, professional dedication and good communication skills.

Job responsibilities:

1. Participate in the formulation of the company's development strategy and annual business plan, formulate the annual production plan and budget of medical devices and purification workshop, and organize the implementation to ensure timely supply;

2. Be responsible for the supervision and management of the work in the production workshop, and organize the formulation and optimization of production, equipment, safety, environmental protection and other systems;

3. All rules, regulations and operating procedures are effectively implemented to ensure that all links in the production process meet the relevant requirements of national laws and regulations;

4. Organize the formulation of various processes, systems, specifications and relevant management measures, and organize the supervision and inspection of their implementation to ensure the overall operation efficiency;

5. Ensure that the plant, facilities and equipment are in good condition and maintained regularly to ensure their good operation;

6. Be responsible for the performance management, key talent training, recruitment and training of the production department;

7. Be responsible for establishing and maintaining public relations between governments at all levels and functional departments to create a good external environment for the company's production and operation.

8. Familiar with assembly line

Qualifications:

1. Bachelor degree or above, major in pharmacy, chemical industry, pharmacy, industrial engineering and other related majors;

2. More than ten years of medical device production management experience, more than two years of working experience in the same position, and working experience in large-scale medical device industry is preferred;

3. Be familiar with the production and operation mode and process of medical devices, and be familiar with relevant equipment;

4. Be familiar with the production management of medical devices and have rich experience in certification and inspection;

5. Be familiar with medical device production, quality management and relevant regulations and knowledge of occupational safety, health and environmental management system;

6. Have good organization, management and coordination ability, and be good at handling public relations related to the factory;

7.Have a high sense of responsibility, excellent leadership, and be able to effectively organize and manage the team.

Job responsibilities:

1. Assist the Department Manager to participate in the annual department work plan and provide support for the annual quality work plan and decision-making;

2. Organize the establishment and improvement of the company's quality management system and quality inspection system;

3. Sorting and analysis of quality data to provide management basis for quality management decision-making;

4. Participate in supplier management and provide technical support;

5. Be responsible for product quality control, preparation of inspection documents and treatment of nonconforming products;

6. External audit cooperation;

Job requirements:

1. Bachelor degree or above in mechanical, electrical and medical equipment;

2. More than 2 years working experience in medical device industry;

3. Be familiar with quality management system and microbial environmental control knowledge; Familiar with ISO13485 regulations;

4. Master office software, have basic network knowledge and good English;

5. Be familiar with and be able to correctly implement relevant national laws, regulations and rules; Participated in the training of relevant laws and regulations;

6.Good communication and coordination skills, problem-solving ability, down-to-earth and willing to work with a sense of responsibility.

Job responsibilities:

1. Participate in the preliminary project investigation, product demand definition, scheme design analysis, etc;

2. Be responsible for the development and design of new products, and complete three-dimensional design, drawing, production assembly, test verification and optimization;

3. According to the development process of medical devices, output various technical documents of the R & D process (product technical requirements, analysis and calculation, process flow, test methods, drawings, BOM, etc.);

4. Be responsible for the design of tooling required in the R & D process;

5. Participate in mold design and automatic equipment transformation of product process.

Job requirements:

1. Bachelor degree or above, major in mechanical engineering, more than 2 years of relevant working experience;

2.Master mechanical theoretical knowledge, be familiar with machining and other processes, and be able to carry out mechanical design independently;

3. Be able to skillfully use SolidWorks, AutoCAD and other drawing software;

4. Excellent leadership, organization, judgment, decision-making, coordination, influence and excellent team management ability;

5. Have a high sense of responsibility and professionalism.

Job responsibilities:

1. New product process design and development and production transfer to ensure the manufacturability of the process and the stability of quality.

2. Improve the product process, improve the product quality and reduce the production cost, and continuously improve the production process: including improving the product performance and stability, improving the tooling and die design, etc.

3. Improvement and maintenance of product qualification rate: collect unqualified data, analyze the causes of unqualified products and take corresponding corrective and preventive measures.

4. Daily process supervision: supervise and guide the standardized implementation of production process; Timely deal with all kinds of production abnormalities in the production process to ensure the smooth progress of production.

Job requirements:

1. Bachelor degree or above, major in machinery and materials.

2. At least 1 year working experience in the production process of active medical devices (experience in high-frequency electric knife products is preferred).

3. Good English listening and speaking, proficient in reading and writing.

4. Understand the management methods, tools and other quality tools of lean production.

5.Strong innovation, analysis and insight, good communication and organization skills.

Job responsibilities:

1. Be responsible for the application and registration of the company's products;

2. Arrange the registration progress according to the company's product planning, and be responsible for supervising the whole process of product registration;

3. Be responsible for drafting and preparing standardization documents, confirming and submitting registration applications;

4. Be responsible for the preparation and review of registration materials to ensure accuracy;

5. Be responsible for communicating with relevant regulatory departments to influence and promote the formulation and implementation of relevant national policies;

6. Be responsible for communicating and coordinating with relevant experts and departments on registration matters;

7. Be responsible for cooperating with R & D and production departments to formulate various standards of products.

Job requirements:

1. Have experience in medical device product registration and have received training in relevant medical device regulations;

2. Be familiar with and master the relevant laws and regulations and technical guiding principles of medical device management and registration in China;

3. Be familiar with all aspects of registration and declaration, and have good ability to write and review declaration materials;

4. Have good communication and coordination skills and be good at handling customer relations;

5. Have strong independent working ability, team spirit and high work enthusiasm;

6. Good English reading and writing skills.