北京招聘

职位描述：
Key accountabilities:
1. Supervise all production activity meet the requirement of GMP and company standards.
管理所负责工段生产事宜，保证生产符合GMP和公司标准的要求
2. Plan and implement production schedules and shift patterns to ensure most efficient use of resources and costs against agreed stock levels;
制定并执行生产计划及班次安排，保证各类资源的有效利用及成本控制；
3. Ensure the efficient collaboration and co-ordination between relevant departments including QA, purchasing, engineering and technical
确保与QA、工程、采购及技术等部门的合作并协调与这些部门间的关系；
4. Coordinate the implementation of new products into production with consideration of compliance to cGMP and other regulations requirements
协调新产品导入并确保符合GMP及其他法规要求；
5. Manage a program of continuous improvement of efficiency and quality on the production processes；
不断优化生产流程，提升质量及生产效率；
6. Prepare and monitor production budget and the production capital purchase requirements;
制定并跟踪生产相关预算及固定资产投资计划及采购需求
7. Develop and manage standard operating procedures system for production operations;
制定并管理生产部标准操作文件体系；
8. Actively support risk assessment activities to ensure that existing and newly implemented manufacturing equipment, process are effective, monitored and safe to use;
积极支持风险评估活动，确保现有及新进设备和流程的有效性、安全性及受控状态；
9. Investigate and rectify deviation in responsible area
调查和矫正生产过程的偏差
10. Check and release the BPR
复核和释放生产记录文件
11. Perform Validation & Revalidation activity.
执行验证或再验证工作
12. Co-ordinate and support the maintenance and repair.
协调和支持设备的维护和维修
13. Manage the position training system to ensure people qualification meet the position requirement
负责员工岗位培训，确保员工符合岗位要求；
14. Act as a SHE representative to identify and understand the SHE risk factors within the production, review SHE issues and performance periodically
识别掌握部门内的SHE风险，定期回顾SHE事件和绩效；
15. Other tasks assigned by supervisor.
完成上级领导临时交给的其它工作任务。

Requirements:
1. Bachelor degree or above.
本科或以上学历；
2. At least 6 years working experience in a pharmaceutical or medical device manufacturing plant with more than 3 years production management position;
6年以上制药或医疗行业工作经验，3年以上管理经验；
3. Familiar with cGMP and other regulation requirements
熟悉GMP及相关法规要求；
4. Fluent English in both oral and written
流利的英语说写能力
5. Problem solving skills
解决问题的能力
6. Coaching and motivating skills
辅导和激励团队的能力
7. Cross-functional collaboration skills
跨部门合作的能力
8. Learning capability
学习能力 举报 分享

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。