华大集团｜注册实习生 (Registered intern)(J26701)

1、负责收集和整理产品注册所需的各类技术文档和资料，确保其准确性和完整性。 2、根据国内外医疗器械和电子产品注册法规和标准，编制并提交产品注册申请文件。 3、与研发、生产、质量等部门密切合作，确保注册所需的技术支持和数据支持。 4、跟踪注册申请的审批进度，及时与监管机构沟通，解决注册过程中出现的问题。 5、学习和了解最新的注册法规和标准，确保公司的注册工作始终符合法规要求。 6、协助注册主管进行注册工作的总结和分析，提出改进意见和建议。 1. Be responsible for collecting and organizing various technical documents and materials required for product registration, ensuring their accuracy and completeness. 2. Prepare and submit product registration application documents according to the regulations and standards of domestic and foreign medical device and electronic product registration. 3. Work closely with R&D, production, quality, and other departments to ensure the required technical and data support for registration. 4. Track the approval progress of registration applications, communicate with regulatory agencies in a timely manner, and solve problems that arise during the registration process. 5. Learn and keep up with the latest registration regulations and standards, ensuring that the company's registration work always complies with regulatory requirements. 6. Assist the registration supervisor in summarizing and analyzing registration work, and provide suggestions for improvement.

1、硕士及以上学历，生物医学工程、医疗器械专业背景; 2、具备良好的文档整理和编辑能力，能够熟练使用办公软件; 3、责任心强，有优秀的沟通、协调能力和组织能力，抗压能力强； 4、英语听说读写流利者优先. 1. Master's degree or above, with a background in biomedical engineering or medical device majors; 2. Possesses good document organization and editing skills, and is proficient in using office software; 3. Strong sense of responsibility, excellent communication, coordination, and organizational skills, and able to work well under pressure; 4. Preference for fluent English speakers (listening, speaking, reading, writing).