HuaRen Pharmaceutical 合规 jobs (salary & requirements)

HuaRen Pharmaceutical 合规 salary range: 8K - 10K, where 100% of positions earn ¥8-10K

￥8-10K

100% of positions earn

Note: the average salary is analyzed based on job postings published by the company. We recommend reviewing it together with position type, education, region and experience.

HuaRen Pharmaceutical 合规 salary changes over the years

Note: the data depends on salary samples of online job postings in the corresponding years and does not fully represent the actual situation within the company. For reference only.

Education requirements: 硕士 is the most common

100% 硕士

What education does HuaRen Pharmaceutical require for 合规 positions? 硕士占比最多，占100%

Salary by education

硕士￥9.0K

HuaRen Pharmaceutical 合规 salaries by education: 硕士 ¥9.0K.

Experience requirements: 5-10年 is the most common

100% 5-10年

What experience does HuaRen Pharmaceutical require for 合规 positions? 5-10年占比最多，占100%

Salary by experience

5-10年￥9.0K

HuaRen Pharmaceutical 合规 salaries by experience: 5-10年 ¥9.0K.

HuaRen Pharmaceutical 合规 hiring regions: mainly 合肥

合肥￥9.0K 100%(2)

In which cities does HuaRen Pharmaceutical have offices for 合规 positions? The main distribution is as follows: 合肥 accounts for 100%. Click this module to view the proportions of other cities, based on job postings in the past year. For reference only.

HuaRen Pharmaceutical 合规 hiring trends over the years

HuaRen Pharmaceutical 合规 changes in hiring volume over the years

What does HuaRen Pharmaceutical 合规 do

Based on related job postings of HuaRen Pharmaceutical in the past year

药品研发合规经理
合肥-包河区 | 5-10年 | 硕士以上 | 2026-03-21
6000-12000元

任职要求：
1、药学相关专业本科以上学历，从事研发QA工作5年以上，2020年后有项目核查经验者优先;
2、熟悉研发质量管理体系要求，有较强的文件撰写能力;
3、具有强烈的责任心、独立工作能力、沟通能力，较强的团队合作能力和学习能力。
岗位职责：
1、负责建立、维护研发中心质量管理体系运行，并持续改进。负责监督研发中心研制开发工作按规程进行，保证研发工作过程中的完整性、真实性、规范性。
2、负责组织研发中心体系文件的审核、修订、分发、回收、销、借阅等工作，按文件体系的类别有序建立文件档案;监督各部门对于研发中心体系相关文件的执行情况。
3、负责实验室日常监督管理工作。
4、负责变更过程审核，批准微小变更的实施措施及变更关闭负责审核异常、偏差的调查和处理;审核 008、00T调查的结果。负责监督物料管理人员的物料管理情况。
5、负责组织迎接国家局、省局关于药品研发的各项检查、核查工作及外部审计工作。
6、负责监督档案管理人员的档案管理情况。
7、负责研发相关文件、记录、方案、报告的审核。
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