Job Description

● Support commissioning and validation of new factory automation systems, takeover and manage the BMS and EMS systems;

● Takeover and manage the operations and maintenance of other automation systems (such as high-efficiency plant rooms, chiller and air compressor cluster control systems);

● Technical upgrades of automation systems, gathering user requirements, providing solutions, and project implementation and management;

● Communication within the company and with external suppliers;

● Familiarity with pharmaceutical GMP regulations and related industry standards, including the ability to draft URS and IOQ protocol, and initiate and follow up on change processes; Support and cooperate with internal and external GMP audits, and be able to appropriately address relevant findings or issues during the audit process;

● Strictly adhere to the company's GMP, Code of Conduct, SHE, and compliance policies and standards, as well as those supporting policie...

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