KEY ACCOUNTABILITIES:


1.负责工艺设备自动化板块运行工作，并提升团队运营能力。


Responsible for the operational work of the process equipment automation section and promote the standard of team work .





2.负责DS和DP板块工艺设备自动化问题调查与解决，偏差、变更和配置变更相关工作。


Responsible for the investigation and resolution of automation issues for DS and DP section, responsible for the relevant deviations, changes and configuration changes.





3.积极参与和引导公司自动化控制系统的发展，努力提升公司自动化控制的技术水平。


Participate in the development of automation system, promote the technical level for automation.





4.负责自动化控制系统SOP文件的起草和批准。


Responsible for drafting and approving the document of automation control system.





5.确保团队在工作中对EHS、GMP和其它监管法规的合规性。


Make sure all the work of group comply with EHS、GMP and other regulations.





6.参与公司的客户审计工作，回答客户在审计中的提问和缺陷整改的答复。


Participate in the audit work for customers, investigate and answer the questions during the audit.





7.完成公司主管布置的其它任务。


Complete other works assigned by supervisor


REQUIREMENTS:


至少有8年以上的药厂工作经历，5年以上的工程部经历；


At least 8 years working experience in pharmaceutical factory, more than 5 years in engineering department.


良好的团队合作和协调能力，良好的语言表达和组织能力，较好的人际沟通能力；


Good team cooperation & coordination ability, good language expression & organization ability, good interpersonal skills.


熟练使用CAD和Office操作软件；


Familiar with CAD & Office software operation.





EDUCATION (Indicate the mini. requirement & preferred discipline):


全日制本科以上文化程度，制药、机械、机电一体化专业的优先考虑；


Full time bachelor degree or above, major in pharmacy, machinery and Mechatronics is preferred.



OTHER SKILLS, ABILITIES & EXPERIENCE:


经历过GMP认证工作，有FDA cGMP或EU GMP认证经历者更佳。


Experienced the GMP certification, the FDA cGMP or EU GMP certification experience is better.