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...