化学药制剂液体制剂吸入制剂药物研发分析方法注册申报 1. Responsible for the development, validation, and routine testing of analytical methods during the drug R&D process.
负责药物研发试验过程中，分析方法的开发、验证以及日常检验工作；
2. Responsible for preparing experimental records, protocols, reports, and other experiment-related documents, ensuring their authenticity and integrity. Also responsible for establishing and reviewing quality standards.
负责完成实验记录、方案、报告及实验相关文件的编写，保证其真实性和完整性；并负责质量标准的制定、复核等工作；
3. Develop project R&D plans, coordinate their execution, and analyze and resolve any issues that arise during the R&D process in a timely manner.
制定项目研发计划并协调计划的执行，对研发中出现的问题进行分析并及时解决；
4. Compile and prepare corresponding registration dossiers in compliance with the latest pharmaceutical registration regulations and guidelines.
根据最新药品注册法规要求整理并编写相应的注册申报资料；
5. Oversee the daily management of the analytical laboratory and perform routine maintenance on analytical instruments.
负责分析实验室的日常管理工作，并对分析仪器进行日常维护；
6. Coordinate the preparation of technical documentation and facilitate technology transfer activities.
协调技术资料撰写及技术转移。
任职要求：
1. Minimum of 3 years of experience in an analytical R&D role.
在分析研发岗位拥有至少3年的工作经验。
2. Comprehensive analytical experience with two or more liquid dosage forms; prior experience with inhalation products, ophthalmic solutions, or injections is highly preferred.
具有2个或以上的液体制剂的完整分析经验；有吸入制剂、眼科溶液或注射剂经验者优先。
3. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
精通微软Office办公软件。