药品注册经理助理（兽药）

1. 协助部门经理处理国内兽药注册、文号申报等相关事务；
Assist the department manager in handling domestic veterinary drug registration, application for approval numbers, and related matters.
2. 根据注册相关要求，编撰和核对注册材料内容，确保注册资料符合相关要求；
Compile and review registration materials according to regulatory requirements to ensure compliance.
3. 负责按照不同市场要求整理出口兽药产品的英文注册资料；
Prepare English registration documents for veterinary drug exports based on market-specific requirements.
4. 协同市场部负责国内外上市产品标签、说明书等的撰写、审批工作；
Collaborate with the marketing department to draft and review labels, package inserts, and other materials for products launched domestically and internationally.
5. 及时获取并传达新法规、新条例，确保注册工作及时跟进。
Stay updated on new regulations and guidelines and disseminate information promptly to ensure timely adaptation of registration workflows.
6. 完成上级领导交办的临时工作；
Complete ad hoc tasks assigned by superiors.


任职要求Qualifications
1. 动物医学、动物药学、药学相关专业，本科及以上学历；
Bachelor’s degree or higher in Veterinary Medicine, Veterinary Pharmaceuticals, Pharmacy, or related fields.
2. 较为熟练的英语读写能力；
Proficient English reading and writing skills.
3. 熟练应用计算机办公；
Proficiency in office software applications
4. 良好的沟通协调能力，团队协作能力和执行能力。
Strong communication, coordination, teamwork, and execution abilities.
5. 了解兽药相关管理法律法规，有国内或国外兽药注册申报经验者优先。
Knowledge of veterinary drug regulations; familiarity with domestic or international veterinary drug registration processes preferred.




外企直招，该职位入职即缴全额五险一金，周末双休，节假日休息，节假日福利，年度体检，年度团建，年假等等