Job Responsibilities

1. Responsible for close communication and cooperation with other engineers, fully understanding the technical solutions, preparing, reviewing and improving the patent technical deliverables;

2. Responsible for patent writing, patent search, cooperating with R&D personnel to discover technical innovation points and patent avoidance design, ensuring the adequacy, completeness and validity of patent documents;

3. responsible for patent application related work such as patent examination opinion response;

4. Responsible for leading the analysis of intellectual property results of R&D projects, exploring the patentability of R&D process and results, conducting patent search and analysis, patent mining and patent layout;

5. Responsible for the daily maintenance of applied patents, assisting in patent application, payment of fees, priority examination declaration and other process affairs;

6. Responsible for the management of intellectual property files and intellectual property rules and regulations;

7. Regularly train R&D engineers on IPR and patent interpretation to ensure that engineers have basic IPR awareness and knowledge;

8. Responsible for R&D other related technical documentation work, including the preparation, review and maintenance of various documents;

9. Other work arranged by superiors.

Job Qualifications

1. Bachelor's degree or above in biomedical engineering, communication or electronics, clinical medicine, physics, computer or software engineering, information management or other related bachelor's degree, master's degree preferred;

2. 2 years of IP related work experience, familiar with patent mining, patent layout, patent writing/review, patent process;

3. proficient in using office software, with very strong writing skills and logic;

4. Ability to search, read and analyze patent and technical literature in English and Chinese;

5. excellent English reading and writing skills;

6. Familiar with IP-related laws and regulations as well as the regular process and latest policies of patent filing;

7. work conscientiously, meticulously and rigorously, with strong learning ability;

8. Excellent communication and collaboration skills, able to work with a team as well as independently;

9. Self-driven, self-learning, curious, willing to challenge, and result-oriented. 

Job Responsibilities

1. Responsible for the collection, summary and analysis of product quality data;

2. Supervise the inspection process of various parts and components to ensure that the inspection of parts and components is carried out smoothly and in a timely manner;

3. responsible for processing and improving production line problems, customer feedback problems and supplier problems;

4. responsible for the establishment, implementation and tracking of all product and material related quality improvement measures for corrective and preventive measures and validation;

5. Participate in inspection and verification, including incoming inspection, process inspection, and material and process verification;

6. Participate in the conversion of products, write and maintain inspection-related SIPs, and systematically manage the documentation related to conversion;

7. Participate in optimizing the process of quality management;

8. handling customer complaints and other related issues;

9. Temporary travel is required.

Job Qualifications

1. Bachelor degree or above in science and technology such as biomedical engineering, electrical and electronics, computer, etc;

2. at least 2 years of experience in medical device quality work or hardware testing work;

3. familiar with ISO9000/ISO13485 quality management system;

4. meticulous and rigorous work style, teamwork spirit, stress resistance and strong execution, positive work attitude;

5. Clear language skills and significant copy editing skills.

Job Responsibilities

1. Develop quality control plan and monitor material quality according to material quality target;

2. responsible for IQC and production line material quality problems, help suppliers to analyze the causes and propose improvement measures;

3. Assist quality and suppliers to develop and unify product quality inspection standards and track the effectiveness of standards implementation;

4. responsible for new suppliers and regular supplier reviews, organize and promote the verification of supplier FA samples;

5. supplier performance management;

6. Monitor supplier change management to ensure that changes are reasonably evaluated and implemented;

7. Complete other tasks assigned by superiors on time and efficiently.

Job Qualifications

1. Mechanical and electrical, electronics and other related majors, college degree or above;

2. at least three years of experience in supplier quality management;

3. Strong communication and negotiation skills;

4. Familiar with processing technology, machining, sheet metal, plastic, PCB/PCBA, raw materials, etc.;

5. Have ISO19001 or ISO13485 system certification;

6. Knowledge of 8D, 5 tools, and QC7 techniques and other quality tools;

7. clear language skills and significant copy editing skills, and proficiency in technical English;

8. Have the ability to coordinate and work independently as well as with a team.

Job Responsibilities

1. Make product competitiveness analysis based on market information, develop product development roadmap, set priorities for CT product development for R&D team, segment product markets and position products in the market;

2. Produce product brochures, product training materials, white papers and other marketing campaign materials;

3. working with expert physicians and setting up product demonstration windows;

4. Participate in the full lifecycle of a new product, from product definition, market demand through product approval, clinical trials, customer installations, and product launches;

5. Understand the competitive market situation, communicate customer needs and competition to the company and translate them into product features;

6. Coordinate with engineers responsible for R&D on product technical features and functions;

7. responsible for verification and confirmation of product functions and features through laboratory tests, clinical trials and other required means;

8. Responsible for writing various documents related to the product including user manuals, maintenance manuals, installation manuals, dismantling manuals and technical reference manuals.

Job Qualifications

1. Bachelor's degree or higher in technology, engineering, or medicine, MBA preferred;

2. more than five years of experience in the medical device industry involving business, technical, engineering or clinical relevance;

3. more than two years of experience in DR, CT and other X-ray products;

4. strong technical knowledge of medical imaging equipment;

5. excellent project management experience and results-oriented work style;

6. Excellent communication and collaboration skills, able to work with a team as well as independently.

Job Responsibilities

1. responsible for the customer site equipment in place, connection, installation and commissioning and other work;

2. Responsible for the maintenance and repair of customer site equipment, maintenance and other work;

3. Assist in the preparation of product technical documentation, so that the new product has a complete technical manual for installation, repair and maintenance;

4. standardize the installation and commissioning of equipment, spare parts replacement and repair in accordance with technical documentation requirements;

5. on-site maintenance service data collection and statistics, regularly provide system failure data for the company's relevant departments for improvement;

6. responsible for cooperating with and assisting in after-sales product application training;

7. Complete other work tasks assigned by superiors on time and efficiently.

Job Qualifications

1. Bachelor degree or above in biomedical or mechatronics, electronic and automation control background;

2. at least 2 years of experience in field repair and maintenance of medical equipment, or similar medical products;

3. good foundation in electronic circuits and automatic control;

4. Excellent fault analysis and troubleshooting skills, on-site fault emergency handling ability and good customer communication skills.

Job Responsibilities

1. Familiar with and deeply understand the market and competitor situation and related business process in the responsible area;

2. familiar with and deeply understand the positioning of the company's products in the market; collect and analyze the dynamics of competing products, sort out the differentiating features with competing products, and have a deep understanding of them;

3. Dig out and deeply understand the distribution of personnel of competing companies in the corresponding regions and organizational structure, summarize the manpower strategy and implementation plan suitable for the company's sales personnel at each stage of the business end, and implement them in a result-oriented manner;

4. Recruit and set up local business teams according to the geographical differences of the business end and the company's business objectives for each region;

5. Provide all-round training to the business team, including but not limited to the company, products, business model, business strategies, implementation methods, etc;

6. Fully utilize the company's cultural sword to unite the business team and give them a deep sense of mission, while identifying business personnel who match the company's culture and cultivating core business backbone personnel;

7. Based on the understanding of the industry, coordinate various resources, deep plowing the industry channels at the business end, collecting and digging market information, intention information, relationship mapping, etc. in the industry to provide the sales team with a full range of services and guarantees to achieve performance;

8. Other work as explained by the leadership.

Job Qualifications

1. Bachelor degree or above, more than 3 years of work experience in recruitment or HRBP direction, or more than 1 year of sales-related work experience in the medical industry;

2. have certain communication and influence on business personnel and channels in the industry, with the ability to dialogue and make suggestions;

3. excellent communication skills, logical analysis ability and good personnel identification ability;

4. be able to assume greater work pressure and adapt to the company's fast-paced work;

5. have strong observation skills and sensitivity to people;

6. have a strong ability to explore and dig;

7. Be able to adapt to short-term business trips. 

Job Responsibilities

1. responsible for the management of the company's quality management system documents, such as document issuance, recycling, scrapping, archiving and other content;

2. responsible for the organization and filing of quality system training records;

3. responsible for the company's monitoring and measuring equipment calibration plan, sending calibration, registration and maintenance of the logo;

4. responsible for the organization and filing of the company's batch records and the initial audit of the batch records;

5. Responsible for the organization and filing of inspection records and the initial audit of inspection records;

6. responsible for the organization and filing of change documents, and responsible for the signature process of change documents;

7. Assist the department head to complete the internal audit of quality management system, follow up the internal audit results, and improve and optimize the quality management system;

8. Assist the department head to draft and revise the product technical requirements, follow up the product registration inspection, and assist in completing the revision of the documents in the registration inspection process;

9. Assist the department head to complete the official GMP, GSP audit;

10. Assist the department head to complete the declaration of registration materials, correction and other work.

Job Qualifications

1. Bachelor degree or above in clinical medicine, medical device, pharmacy, biomedical engineering, mechanical, electronic, English, experience in medical device system or product registration is preferred;

2. Knowledge of ISO9000/ISO13485 system;

3. willing to take the initiative to learn, strong learning ability;

4. Work in a meticulous and rigorous style, have good communication and organizational coordination skills, teamwork spirit, stress resistance and strong execution.

Job Responsibilities

1.Responsible for R&D administrative affairs, and the administrative and personnel interface between R&D and various departments;

2. Responsible for the management and maintenance of R&D information system and documents, application and maintenance of material codes, management of R&D specification documents and technical documents, integrity review and release of R&D output technical documents;

3. Responsible for the management and maintenance of R&D prototypes and materials, procurement and management of R&D materials and items, supervision of 5S in R&D labs, R&D procurement process handling and follow-up, etc.;

4. Assist in R&D project management, responsible for the regular collation and analysis of various R&D reports, participate in the coordination and management of related matters, assist in the development and implementation of departmental management rules and regulations and various processes, and process feedback and optimization;

5. Arrangement of departmental meetings, preparation of meeting minutes, follow-up and supervision of meeting resolutions;

6. Complete other work as explained by superiors.

Job Qualifications

1. Bachelor degree or above, 1 year working experience or above, majoring in science and technology or management is preferred;

2. Experience in R&D administration is preferred;

3. Experience in R&D project management or R&D process tracking, and understanding of project management process and R&D process is preferred;

4. Proficiency in using Word, Excel, PPT and other related office software, strong writing and text editing skills, certain data analysis skills, good English reading and writing skills;

5. rigorous thinking, logical integrity, meticulous and conscientious work, a strong sense of responsibility;

6. lively and cheerful personality, with affinity, good at communication, strong coordination skills, organizational planning skills and teamwork spirit;

7. good emotional management skills, excellent stress tolerance;

8. excellent learning ability, good ability to understand and accept new and unknown things;

9. Ability to work with a team as well as independently

Job Responsibilities

1. understand product features, functions, usage processes, performance and specifications, prepare test plans and test cases and build test platforms according to test requirements and test plans;  

2. Participate in the daily debugging, verification and testing of R&D, including but not limited to data acquisition, data analysis, functional verification, system and subsystem testing;

3. solving image quality problems, optimizing image quality and completing image quality tests by working and communicating with other R&D engineers in hardware, software, mechanical, etc.;  

4. Write image quality specifications, develop image quality test methods, and design various models for image quality verification and system diagnostic testing;

5. participate in design evaluation and provide recommendations related to product quality and testability;  

6. Provide technical support to production.

Job Qualifications

1. Bachelor's degree or above in medical imaging, biomedical, software, electronics and other related disciplines, with at least 2 years of work experience;  

2. familiar with software, hardware and precision machinery; 

3. clear language skills and significant copy editing skills;

4. programming development experience in Visual C / C++ or C / C ++ under Linux, and scripting languages including Matlab, C shell, and source code version control tools preferred; 

5. Knowledge of technical English; 

6. experience in testing medical products preferred;  

7. Excellent communication and collaboration skills, able to work with a team as well as independently.

Job Responsibilities

1. engage in the development of medical tomography imaging systems, subsystems, with a focus on image quality of medical imaging systems, including all phases of development and design from concept, architecture, documentation, design, testing, set validation, to quality;

2. simulation of x-ray tubes, x-ray detectors and optical paths, and development of mathematical models for compensating defects in relevant subsystems to improve the image quality of imaging systems;

3. development, optimization and improvement of algorithms for the calibration, reconstruction and image processing of imaging systems;

4. implementation and optimization of computationally intensive image reconstruction and image processing algorithms;

5. expanding system imaging capabilities through interaction with customers, improving customer satisfaction, and bringing the system to a new level of functionality, performance, product reliability and quality;

6. solving image quality problems, optimizing image quality, and completing image quality tests by working and communicating with other R&D engineers in hardware, software, mechanical, and other areas;

7. Write image quality specifications, develop image quality test methods, and design various models and tools for image quality verification and system diagnostic testing;

8. Provide technical support to production.

Job Qualifications

1. master's degree or above in electrical, electronics, computer, biomedical, physics, mathematics and other related fields;

2. familiar with signal processing, image processing, image reconstruction, inverse problems, characteristics of X-rays including attenuation, scattering and beam hardening;

3. working knowledge of image quality requirements for medical imaging products;

4. 3+ years of programming development experience in Visual C / C++ or C / C ++ under Linux, and scripting languages including Matlab, C shell, and source code version control tools;

5. very strong hands-on skills, with the ability to independently design experiments and develop test methods to try and validate new ideas;

6. a very strong mathematical and physical background and computer modeling and simulation skills;

7. proficiency in technical English;

8. experience in medical product development preferred;

9. Excellent communication and collaboration skills, able to work with a team as well as independently.

Job Responsibilities

1. Participate in the development, design and validation of the company's large-scale high-end medical imaging-related products;

2. mainly responsible for the above related work in the software/firmware related part of the product, including the embedded software of the control system, FPGA, upper client software, upper test software and other aspects of the design development and verification work;

3. Participate in writing functional specifications for software and firmware design and documentation for verification test specifications;

4. Participate in the testing, transferring and process optimization of related products.

Job Qualifications

1. Master's degree or above, majoring in computer, electronics/circuit, communication/information, mathematics or related science and technology;

2. solid mathematical and professional foundation, spirit of research, good teamwork spirit, and high enthusiasm for learning;

3. familiar with C/C++, Java, Python and other programming languages; with Linux platform, SoC, embedded, FPGA and other related technologies, proficiency in any one of the above technologies is preferred;

4. Familiar with serial communication, JTAG, CAN, SPI, IIC and other interface drivers, familiar with real-time operating systems, multi-threaded programming, bootloader, with interface driver development or operating system development experience is preferred;

5. Familiarity with digital signal processing, image processing algorithms, deep learning algorithms is preferred;

6. Excellent academic performance during the study period is preferred;

7. Participation in electronic competitions or other practical projects during the study period is preferred;

8. Proficiency in using Word, Excel, PPT and other related office software, strong writing and text editing skills, and certain data analysis skills;

9. rigorous thinking, complete logic, meticulous and conscientious work, and a strong sense of responsibility;

10. excellent learning ability, good understanding and acceptance of new and unknown things;

11. Ability to work both with a team and independently.

Job Responsibilities

1. mastering product features, functions, usage processes, performance and specifications, developing test requirements and test plans, preparing test plans and test cases, and building test platforms;

2. Participate in the daily debugging, verification and testing of R&D, including but not limited to data acquisition, data analysis, functional verification, system and subsystem testing;

3. solving image quality problems, optimizing image quality and completing image quality tests by working and communicating with other R&D engineers in hardware, software, mechanical, etc.;

4. Write image quality specifications, develop image quality test methods, and design various models for image quality verification and system diagnostic testing;

5. participate in design evaluation and provide recommendations related to product quality and testability;

6. Provide technical support to production.

Job Qualifications

1. Bachelor's degree or above in medical imaging, biomedical, software, electronics and other related fields;

2. familiarity with software, hardware and precision mechanics;

3. clear language skills and significant copy editing skills;

4. 3+ years of programming development experience in Visual C / C++ or C / C ++ under Linux, and scripting languages including Matlab, C shell, and source code version control tools;

5. proficiency in technical English;

6. experience in testing medical products preferred;

7. Excellent communication and collaboration skills, able to work with a team as well as independently. 

Job Responsibilities

1. Participate in the development, design and validation of the company's large-scale high-end medical imaging-related products;

2. Participate in the testing, transferring and process optimization of related products;

3. Mainly assist in the above related work for the electrical and electronic related parts of the products, including the design and verification of electrical and electronic hardware, embedded software, FPGA and test software, etc.

Job Qualifications

1.Bachelor degree or above, majoring in electronics, electrical, semiconductor, automation, computer or related science and technology;

2. solid mathematical and professional foundation, drilling spirit, good teamwork spirit and high enthusiasm for learning;

3. Familiar with digital electronics, analog circuits, embedded software, FPGA, Python/C/C++ and three-phase electricity and other related technologies, and proficiency in any of the above technologies is preferred;

4. excellent academic performance during the study period is preferred;

5. Participated in electronic competitions or other practical projects during the study period is preferred;

6. Proficiency in using Word, Excel, PPT and other related office software, strong writing and text editing skills, and certain data analysis skills;

7. rigorous thinking, complete logic, meticulous and conscientious work, and a strong sense of responsibility;

8. excellent learning ability, good understanding and acceptance of new and unknown things;

9. Ability to work both with a team and independently.