Talent Recruitment

Job requirements: 1. Bachelor's degree or above, majoring in polymer chemistry and physics, polymer materials related majors, with experience in polymer synthesis, polylactic acid or polylactic acid composite material development preferred; 2. Write R&D, testing, and production documentation reports, proficiently use polymer related testing and production equipment, and analyze results such as testing spectra; 3. A down-to-earth person with a strong sense of responsibility, strong execution ability, a mindset and ability to face difficulties and solve problems, able to grow together with the enterprise. Job responsibilities: 1. Responsible for the synthesis, testing, analysis, and mass production of polylactic acid and polylactic acid composite materials in the biomedical materials laboratory workshop; 2. Independently complete literature review, and based on the literature, complete the preliminary design and optimization design of the experimental plan; 3. Objectively and comprehensively organize and analyze research and development production data, timely report the progress of project topics, and write operational process SOP and testing SOP and related reports; 4. Responsible for drafting relevant inventions and cooperating with patent firms to apply for patent protection. Company benefits: 1. 5-day 8-hour work schedule, meal allowance, and salary interview. 2. Purchase five insurances and one fund, and enjoy various statutory holidays in accordance with the law. Gift subsidies will be provided for holidays such as Mid Autumn Festival and Dragon Boat Festival. 3. Enjoy year-end bonuses and other rich cultural activities, which depend on the company's performance. Excellent performers will receive appropriate dividend incentives. 4. Technology Research Award, a reward measure specifically designed for research and development, incentivizes research and development to achieve more results, depending on the contribution of each person in the field of technology research. Work location: Shenzhen Longhua Guanlan Yinxing Zhijie Phase II Contact phone number: ************* Xiang Dong Company Profile: Shenzhen Lixin Science Co., Ltd. is a high-tech enterprise in the biomedical field jointly founded by overseas returnees, medical device industry professionals, and clinical doctors. It is committed to the development of biodegradable new materials and implanted medical devices in fields such as orthopedics, dentistry, and medical aesthetics. Lixin Science was established on December 13, 2016, with a registered capital of 1.8819 million yuan. The team consists of two high-level talents from Shenzhen. The company won second place in the biopharmaceutical industry finals of the 2018 Shenzhen Innovation and Entrepreneurship Competition, was named a high-tech enterprise in Shenzhen in 2018, and was named a national high-tech enterprise in 2020. The company currently applies for 78 patents, grants 35 patents, including 12 invention patents. Two PCT international patent applications. Since its establishment, the company has received approximately 40 million yuan in financing and has established research and development production centers in Bao'an, Pingshan, and Longhua, Shenzhen. Shenzhen Longhua R&D Center is a biodegradable material R&D and production center, mainly providing materials and design solutions for absorbable medical devices. The company has currently established cooperative relationships with multiple hospitals, including Shanghai Sixth Hospital, Shanghai Ninth Hospital, Shenzhen Nanshan Hospital, Zhongshan Hospital, as well as multiple domestic and foreign universities such as National University of Singapore, Shanghai Jiao Tong University, Zhejiang University, Henan Normal University, and Changzhou University. The company is committed to the development of biomedical biodegradable materials and absorbable implantable medical devices. We welcome aspiring individuals to join us!

Job responsibilities: 1. Assist the market manager in conducting market research, competitor analysis, regularly summarizing market conditions and policy changes, and proposing trend development suggestions; 2. Responsible for product line marketing activities, conference planning, promotion, and implementation in accordance with the company's strategic requirements; 3. Assist in organizing relevant personnel and distributors to receive training on the latest product and market knowledge, and conduct assessments; 4. Assist sales and other departments in completing operational promotion work for end customers and distributors, continuously improve promotion methods, develop promotion plans, plan and produce various market promotional materials; 5. Complete other tasks assigned by superiors. Job requirements: 1. College degree or above in medical or marketing related fields; 2. More than 2 years of experience in marketing and promotion related work; 3. Strong market expansion and communication skills; 4. Strong sense of responsibility, adaptability, and execution ability.

Job Description: 1. Responsible for the structural design of product appearance and core components, as well as the development and updating of new generation products; 2. Responsible for the design of product solutions, formulation of relevant standards, and preparation of BOM; 3. Responsible for the processing and manufacturing management of products and projects; 4. Complete tasks assigned by superiors and cooperate with the R&D team and various departments. 5. Familiar with the product development process and understand the quality management system; Job requirements: 1. Bachelor's degree or above in full-time unified enrollment, with priority given to mechanical and materials majors; 2. Priority given to those with experience in medical device product development and design; 3. Familiar with the use of common CAD software, such as PROE, AUTOCAD, Solidworks, converting 2D/3D drawings, etc., proficient in surface modeling, assembly drawing, drawing and other skills; 4. Familiar with the processing flow of common materials, such as silicone, plastic, metal parts, etc; 5. More than 2-3 years of work experience, with practical experience from design to manufacturing preferred; 6. Have their own insights into product development and design, and be innovative. 7. Proficient in English Test Band 6 or above, with strong English reading and literature search abilities; 8. Work actively, seriously, and proactively, with a strong sense of responsibility; Has a strong sense of teamwork and excellent communication, coordination, and problem-solving skills.

Job responsibilities: 1. Actively participate in the development and clinical research of new medical products, mainly responsible for the clinical research trials of the company's product projects and follow-up work with cooperating hospitals, including animal experiment docking, clinical experiment docking, follow-up and application of industry university research projects, etc; 2. According to the requirements, complete specific research and development, record work, and regularly report work progress, including technical research and exchange in the early stage of the project, feedback on device research and development in animal experiments and clinical practice, and progress in applying for industry university research projects; 3. Collaborate with other departments to prepare and review relevant technical development documents; 4. Complete other tasks assigned by the leader. Qualification: 1. Graduates from medical related majors such as biomaterials and clinical medicine, with a medical background given priority; 2. Priority given to GCP clinical project management; 3. Understand relevant laws and regulations, medical knowledge, and be familiar with the entire process and all aspects of clinical trials for three types or active implantable medical devices; 4. Proficient in using English, good reading and writing skills (CET-6, not mandatory), able to search, read, and summarize Chinese and English literature related to product technology and clinical applications, etc. Bonus points. 5. Can adapt to travel.

Job responsibilities: 1. Carry out registration clinical, trial clinical, and research clinical of company products, including animal experiment docking, clinical experiment docking, industry university research project layout and application for cooperative projects; 2. Interpret and analyze the relevant standards, guiding principles, and clinical literature of domestic and foreign medical device clinical trials; 3. According to the requirements of GCP, product standards, and registration review guidelines, prepare clinical trial plans, as well as subsequent clinical trial reports and clinical evaluation reports; 4. Responsible for monitoring the clinical trial process, completing monitoring reports, protocol violations, and other reports; 5. Develop the company's product marketing strategy and promotion plan, analyze market data and industry policies, provide relevant risks and suggestions, and cooperate with market activity support, 6. Handling emergencies and completing other work tasks assigned by leaders. Job requirements: 1. Medical or pharmaceutical related majors, with a bachelor's degree or above (practical experience in clinical research, surgical research, orthopedic research, and biomedical research is preferred); 2. Familiar with industry knowledge related to CRO, GLP, and GCP, and obtain certificates; 3. Strong logical thinking, good communication and coordination skills, and execution ability; 4. Have good English listening, speaking, reading and writing skills; 5. Has good pressure resistance and can adapt to business trips.