长沙招聘

KEY ACCOUNTIBILITIES:
1. As SOP Coordinator, coordinate with technical staff and QA staff for SOP updating, tracking, conduct the SOP distribution and destruction.。
与技术和QA组合作，负责SOP的更新，统计，执行SOP的落实和销毁
2. Coordinate with BAS Management to review and manage the personnel files, such as CV, JD, Training Record, Training Plan, etc, archive the personnel files annually.
与BA管理层合作，审核和管理员工个人信息（如简历，工作描述，培训记录，培训计划等），并负责这些信息每年一次的归档
3. Coordinate with BAS staff for methodology control.
与内部同事沟通方法学管理
4. As study folder coordinator, print the study folder and coordinate with technical staff for tracking the study folder pages control.
作为项目文件的协调者，负责打印项目文件并统计好这些文件。
5. Coordinate with technical staff and QA staff for tracking the template table version control and CV/JD control.
与技术和QA组合作，追踪CV/JD相关表格模板。
6. Conduct the tracking of methods in BAS Department.
负责部门内部实验方法的跟踪
7. Coordinate with trainer and BAS staff to conduct the new employees training, updated SOP training and refresh training, provide necessary training to BAS member.
负责组织协调BAS新员工的培训以及为BAS员工提供SOP更新，新的培训后
8. Conduct the tracking of projects in BAS Department.
负责部门内部项目的跟踪
9. Update the GLP organization chart monthly.
每月更新GLP组织结构图

REQUIREMENTS:
1. BA degree or above in English 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.

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。