长沙招聘

KEY ACCOUNTIBILITIES:
1. Conduct experimental phase inspection and data audit to all studies
2. Follow up the corrective action to assure all findings are timely corrected.
3. Conduct QC review of study raw data and report.
4. Conduct facility inspection routinely to maintain consistent high level of compliance.
5. To ensure laboratory equipment and systems are suitable for use.
6. Conduct process audit for Equipments, Software, Logbook, Solutions and Reagents, Environment.
7. To ensure that records are made manually or by recording instruments which demonstrate that all the required testing procedures were actually carried out
8. 对项目进行实验阶段性检查和数据审核。
9. 及时跟进项目，确保所有项目出现的问题得到及时改正。
10. 对项目的原始数据和报告进行审核。
11. 负责实验室设备的日常检查，确保其高标准运行。
12. 负责保持实验室的所有设备和仪器正常工作。
13. 对实验室仪器，软件，实验记录本，溶液，试剂及环境进行日常检查。
14. 负责所有的实验相关的记录都由手动或仪器记录下来，以验证所有要求的实验步骤得到执行。

REQUIREMENTS:
1. BS degree or above in Analytical, Biology or related field.
2. Must be trained in or have experience with the requirements of the FDA GLP regulations and OECD GLP guidelines.
3. Strong communication skills, both written and verbal, and outstanding interpersonal skills are essential job requirements.
4. Must be able to openly share information and work in a team-oriented manner in order to accomplish performance objectives.
5. Must be familiar with process of bio-analytical studies.
6. Be skillful at reading, understanding and writing English documentation.
7. 本科及以上，生物分析或者相关专业
8. 有FDA GLP或者OECD GLP相关培训或者工作经验。
9. 有较强的沟通能力，口头表达能力和书写能力，善于与人交际。
10. 有团队精神，善于团队合作，完成工作任务
11. 熟悉生物分析相关的步骤
12. 较强的英语读写能力

药明康德是国际领先的开放式能力与技术平台公司，为全球制药及医疗器械等领域提供从药物发现、开发到市场化的全方位一体化的实验室研发和生产服务。本着以研究为首任，以客户为中心的宗旨，药明康德通过高性价比、高效率的服务平台帮助全球客户缩短药物及医疗器械研发周期、降低研发成本。药明康德平台涵括化学药研发和生产、细胞及基因疗法研发生产、药物研发和医疗器械测试等，正承载着来自全球30多个国家的3500多家创新合作伙伴的数千个研发创新项目，致力于将最新和***的医药和健康产品带给全球病患，实现“让天下没有难做的药，难治的病”的梦想。