1、Support the design and implementation of computer systems for new filling project of Lilly Suzhou site；
2、Ensure Lilly GQS 200 Series Standards and LQS-302 are followed appropriately for computer systems/automation and all compliance requirements by regulatory agencies are met；
3、Ensure that computer systems are validated and remain so throughout the lifecycle of the system；
4、Ensure manufacturing and support operations are kept up to date with changes to current Lilly Corporate CSV requirements；
5、Approve Computer System & Automation related documents listed but not limited as assessment documents, any remediation plans, validation deliverables and periodic review documents；
5、Provide the Quality subjects expertise during internal/external audits of computer；
6、Support the implementation of SAP and PMX as needed；
7、To be responsible to build up quality culture；
8、To assume other tasks related to QA。

1、Bachelor degree or above, majored in pharmaceutical, computer science / automation, engineering or related science；
2、Three years or above experience in computer system validation support or QA；
3、Capable of speaking, writing and reading in English。