For the global medical beauty market to bring safer and more effective medical beauty photoelectric equipment and diagnosis and treatment integrated solutions
1. Responsible for the development of hardware systems for related products, completing hardware system scheme design, component selection, schematic drawing, and partial PCB layout work;
2. Assembly, debugging, verification, and related design outputs during the R&D phase;
3. Responsible for implementing or reviewing component selection, schematic drawing, and PCB compliance with the company's quality management process, writing design specifications, testing procedures, testing reports, and other engineering design documents; Ensure that the product complies with regulatory requirements
4. Responsible for pre research of new technologies, tracking of cutting-edge technologies in the industry, and submission and verification of innovative solutions
5. Responsible for managing the risk analysis of product hardware systems, resolving EMC and safety issues related to products, and assisting in the registration and certification of related products;
6. Responsible for pre research of new technologies, tracking of cutting-edge technologies in the industry, and submission and verification of innovative solutions
7. Complete other temporary tasks assigned by the leader.
1. Having independent research and development work experience; Having solid knowledge of digital and analog circuits, proficient in the design, simulation, debugging, and testing methods of commonly used hardware circuits;
2. Capable of independently decomposing comprehensive circuit requirements based on product requirements, designing, simulating, and verifying circuit solutions according to circuit specifications;
3. Proficient in key parameter indicators of commonly used components, with a deep understanding of product reliability design, EMC design, maintainability/repairability design, and purchasable/producible design;
4. Proficient in schematic and PCB design tool software, proficient in PCB layout, wiring, etc; Proficient in solving common EMC and safety issues;
5. Proficient in using conventional instruments and equipment such as oscilloscopes, signal generators, spectrum analyzers, etc;
6. Experience in EMC and safety regulation rectification, and experience in medical industry research and development are preferred;
7. Has strong logical analysis ability, hands-on ability, communication ability, and teamwork ability.
1. Participate in medical device software requirement analysis and be responsible for building the system software framework design;
2. Complete the design, implementation, improvement, and debugging of product software, and compile and update relevant technical documents according to specifications;
3. Responsible for MCU software code writing, debugging, testing process, troubleshooting logic faults, and ensuring software system stability;
4. Submit high-quality code according to the project plan, conduct software debugging work, and complete development tasks;
5. Ability to develop and test one's own code;
6. Responsible for writing technical documents related to development and mass production, as well as maintaining code versions;
7. Collaborate with hardware engineers to analyze and solve problems encountered during development and mass production processes.
1. Proficient in C language, familiar with various mechanisms of embedded systems, familiar with basic algorithms and data structures, able to use software libraries provided by manufacturers for rapid development;
2. Proficient in the development process and methods of RISC-V core and Cortex-M core MCU, with experience in developing and debugging similar products;
3. Familiar with various embedded product interfaces such as USB, SPI, I2C, UART, etc., able to understand conventional circuit schematics, familiar with control methods of conventional devices;
4. Good coding habits and technical document writing skills, excellent communication skills, and strong teamwork spirit;
5. Experience in medical device development is preferred.
1. Responsible for project management of the company's medical device clinical trials, conducting comprehensive quality control and progress management of the clinical research projects under responsibility, ensuring that all trials are strictly conducted in accordance with the clinical trial protocol, standard operating procedures/internal operating procedures, and Chinese laws and regulations;
2. As the main liaison for clinical trials, representing the company and project team to maintain timely and effective communication with third parties, institutions, and other units, ensuring the accurate and complete transmission of important project related information, and cultivating and maintaining good relationships with the center and clients;
3. Conduct comprehensive quality control and management of the clinical research projects under responsibility, supervise the timely completion of the comprehensive initiation, execution, and completion of clinical trials, and communicate and coordinate with personnel from other departments in a timely manner;
4. Develop a project management plan, determine the scope of responsibilities, team members, schedule, financial budget, etc. for clinical research, and continuously review and modify the project management plan during the project to ensure that the clinical research meets the schedule requirements and controls the project scope and budget within the contract scope;
5. Responsible for timely communication with superiors, conducting comprehensive assessments of the selection of experimental centers and researchers for ongoing and potential future projects, and developing experimental budgets, and regularly reporting experimental progress. Identify, monitor, and promptly respond to various risks during the project process, and accurately assess the overall impact of corresponding risks on the project;
6. Have the responsibility scope of PM or CRM and be able to handle emergency incidents in a timely manner;
7. Responsible for reviewing the processes and forms required for clinical trials to ensure compliance with regulatory requirements;
8. Other tasks assigned by the leader.
1. Bachelor's degree or above in clinical medicine or related majors;
2. At least 3 years of clinical research experience and at least 1 year of project management experience in large equipment companies or CRO companies;
3. Those who have knowledge of products in the field of dermatology, have certain insights into relevant regulations on clinical trials at home and abroad, and have practical experience and skills are the best;
4. Has a sense of responsibility and enterprising spirit, communication and coordination skills, analytical and problem-solving abilities, and teamwork spirit.
1. Responsible for promoting and selling the company's medical beauty and medical device products, and completing sales tasks;
2. Through daily visits and other academic activities, explore potential customers, establish and maintain good cooperative relationships;
3. Establish and improve customer records, and promptly follow up on daily sales work;
4. Complete other tasks assigned by the leader.
1. More than 2 years of experience in medical device sales, with experience in dermatological product sales or medical device/equipment industry preferred
2. Good communication and coordination skills, good customer service awareness, and teamwork spirit;
3. Strong sense of responsibility and ability to withstand pressure.
1. Experience in coordinating the introduction of new products or project development;
2. Capable of independently developing and reviewing process flow diagrams and SOPs;
3. Have basic project management and communication skills, able to organize teams to analyze, identify and review the causes of defective products during trial production, and promote improvement or resolution of problems;
4. Lead the implementation of engineering changes, continuously improve and optimize production processes and techniques, and improve product yield and production efficiency;
5. Confirmation and improvement of new process technology during trial production;
6. Provide training on new production processes for operators;
7. Other tasks assigned by superiors.
1. Bachelor's degree or above, with a background in science and engineering, proficient in using 3D design software/office software is preferred;
2. Familiar with mechanical drawing software and possess design capabilities;
3. Familiar with electrical engineering, structure, and mold, with rich practical application experience;
4. Familiar with medical device laws and regulations.
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