2. Develop and implement platform content strategies to ensure content quality and compliance, while maintaining unique style and creativity;
3. Plan and execute popular content, attract fan interaction, increase platform exposure, while maintaining the quality and creativity of the content;
4. Manage and optimize video account, increase fan base and interaction volume, while maintaining good interactivity and reputation of the account;
5. Analyze data, track operational effectiveness, optimize content strategies and user experience, and enhance fan stickiness and activity;
6. Collaborate to expand content resources, including but not limited to anchors, partners, etc., while maintaining sensitivity and enhancing platform attractiveness;
7. Track industry trends, maintain a keen sense of trends, enhance the platform's ability to keep up with the latest trends, and win the love of users.
2. Be familiar with the trends of the Internet industry, have good market acumen, and have strong judgment and creativity;
3. Possess good creative thinking, proficient in using hot topics for content creation, improving content quality and creative effects;
4. Possess data-driven thinking, able to optimize content strategies and improve operational effectiveness through data analysis;
5. Possess team collaboration and communication skills, able to work well with team members and partners, and have strong cross team communication and coordination abilities;
6. Have planning and execution abilities, able to allocate work content reasonably and follow up on work progress to ensure the project is completed on schedule.
1. Familiar with food related laws, regulations, and food hygiene requirements, with OEM factory control and audit capabilities;
2. More than 3 years of experience in food factory audits, familiar with knowledge and processing procedures related to food and meat products;
1. Having keen observation skills, efficient execution abilities, and problem-solving skills;
2. Have good quality control literacy, integrity and reliability, and strong teamwork spirit;
3. Adapt to long-term business trips.
1. Responsible for product quality inspection of the company, ensuring the quality of shipped products;
2. Count the number of defective products and report the situation of defective products in a timely manner;
3. Ensure proper handover between products and warehouses;
4. Complete other tasks assigned by the department head.
1. More than 3 years of work experience;
2. Familiar with knowledge of direction inspection of electronic components (resistors, capacitors, diodes, ICs, etc.) and polar materials;
3. Can understand mechanical drawings and proficiently use various measuring and testing equipment, such as calipers, projectors, tensile machines, hardness testers, etc;
4. Proficient in basic operations of EXCEL and WORD office automation.
1. Familiar with product design and testing standards in the medical device industry, such as EMC YY0505 and safety regulations GB9706;
2. Familiar with digital and analog circuits, MCU and RAM peripheral circuit design, pre design various electronic components for products, conduct selection, performance evaluation, specification parameter debugging, measurement and analysis;
3. Proficient in using Lichuang EDA PCB design software, able to independently complete the schematic design of the product according to the expected product use, with a good understanding of PCB layout and production technology, and able to independently complete PCB design;
4. Priority consideration will be given to those with experience in designing related medical device products;
5. Can assist the engineering department in developing installation processes and writing process flow diagrams;
6. Has a certain analytical ability to analyze defects in the production process and improve reporting
1. College degree or above, major in electronics or related fields, with at least 2 years of work experience;
2. Familiar with product design and testing standards in the medical device industry, such as EMC YY0505 and safety regulations GB9706;
3. Familiar with digital and analog circuits, MCU and RAM peripheral circuit design, pre design various electronic components for products, conduct selection, performance evaluation, specification parameter debugging, measurement and analysis;
1. Have a certain hardware foundation, experience in microcontroller development, able to independently undertake development tasks, familiar with MCU architecture programming.
2. Proficient in C language, rich experience in module driven software, able to design software architecture and write code according to product functional requirements.
3. Responsible for software debugging and testing, analyzing and resolving issues during the software development process.
4. Optimize and tailor the software according to project requirements.
5. Write relevant technical documents.
6. Master the mainstream 8-bit, 16 bit, 32-bit microcontrollers or ARM series products on the market, proficiently understand the basic principles of various interface communication, such as USB, I2C, SPI, I2S, UART, CAN, etc.
7. Good coding style, strong logical thinking and problem-solving ability
Has a strong spirit of exploration and creativity, is hardworking, has good work habits and attitudes, good communication skills and teamwork abilities.
1. Have a certain hardware foundation, experience in microcontroller development, able to independently undertake development tasks, familiar with MCU architecture programming.
2. Proficient in C language, rich experience in module driven software, able to design software architecture and write code according to product functional requirements.
3. Responsible for software debugging and testing, analyzing and resolving issues during the software development process.
4. Optimize and tailor the software according to project requirements.
5. Write relevant technical documents.
1. Communicate effectively with the drug regulatory department regarding registration work;
2. Monitor the implementation of domestic regulations and standards;
3. Ensure proper archiving of all documents and certificates;
4. Write and modify product standards and manuals;
5. Declaration of registration materials for medical devices;
6. Cooperate with other departments of the company;
7. Organize company personnel to participate in relevant legal and regulatory training;
8. Other work related to medical device registration applications;
9. Complete registration related tasks temporarily handed over by superiors.
1. Science and engineering majors such as medicine, pharmacy, and bioengineering;
2. More than 2 years of experience in medical product registration and certification, familiar with online application processes such as medical device registration, renewal registration, change, adverse event detection, and enterprise self inspection reports on the Guangdong Provincial Government Service Network is preferred;
3. Familiar with lS013485 or YY0287 GB9706、YY0505、 The Regulations on the Supervision and Administration of Medical Devices, Medical Device Registration and Filing, as well as the laws and regulations issued by the US FDA and EU EMA, can provide relevant regulatory basis for project registration and review;
4. Have certain abilities in literature search and data writing and compilation.
1. Responsible for conducting research and analysis on daily necessities categories according to market demand on various live streaming platforms, and searching for hot selling products
2. Develop and procure products with market potential based on market demand; And make accurate trend judgments on product cycles and prices, coordinate with operations and graphic designers, and create high-quality and competitive listings;
3. Familiarize oneself with the characteristics of each developed product, extract product selling points, and provide information maintenance and updates to operational personnel;
4. Conduct research and assess the existing product market, independently expand and expand product lines, and develop and execute development plans;
5. Track, search, analyze, summarize, and evaluate information on new products, and develop new product lines;
6. Regularly analyze data on self-developed products and be able to adjust sales strategies in a timely manner;
7. Have a clear understanding of platform rules and policies, know how to identify infringing products, and be able to ensure that new products developed will not have any infringement or violation issues. Keep abreast of changes in platform policies and competitor information in a timely manner.
1.1 years of procurement and supplier development experience, sensitive to product prices, and able to conduct inquiries, negotiations, and payment terms negotiations.
2. Experience in e-commerce product development and live streaming product selection is preferred.
3. Familiarize and master various development approaches and techniques, understand how to analyze and evaluate the market size and competitiveness of products, have their own insights into product selection ideas, and provide constructive suggestions for optimizing product sales.
1. Conduct market research, assist the company leadership in identifying project products and developing project development plans;
2. Integrate and manage internal and external resources of the company to ensure smooth implementation of new product design, research and development, testing, and implementation;
3. Estimate potential risks in the project and implement control plans to reduce quality, complaint, and regulatory risks faced by new products entering the market;
4. Complete other tasks assigned by superiors.
1. Bachelor's degree or above, majoring in biomedical, electronic, mechanical, software, communication, engineering management, with English proficiency of CET-4 or above, proficient in listening, speaking, reading, and writing;
2. Priority consideration will be given to those with PMP project management professional qualifications;
3. 5 years or more of experience in R&D and clinical project management in the medical device industry, familiar with ISO13485 and relevant regulatory requirements of China, EU, and South Korea GMP, familiar with product project initiation, R&D, production, and closure procedures;
