Ting Dong Email and Phone Number

Maintain QMS documentation (e.g. SOP, Form, Worksheet and Specification etc.);Perform SOP Periodic Review;Responsible for QMS documentation’s revision;Responsible for aligning SOPs with Corporate Quality Procedure;Control of external documents;Provide new joiner with orientation on GDP;Provide GDP annual training in site level;Launch BPLM electronic signature in site level and complete e-sign training. Completed e-signature manual and inform public path to users;Solve BPLM issue in daily operation of processing;Responsible for archiving all the QMS documents and records orderly by hard copy/electronic system;Create and maintain quality public disk, responsible for tracking;Responsible for Document Control Room normal operation maintenance;Assist in the audit work;Quality data analysis.

Responsible for the production of tables and capsules and quality control.Execute all duties faithfully and responsibly in accordance to SOP and to immediately report all observations of GMP non-conforma nces.Daily record according to SOP.Sampling of Intermediates according to relevant sampling plans or as per supervisors’ direction.Responsible for the accuracy, integrity and reliability of all lab data generated.Responsible for the implementation of self-completed of GMP.To be in process control during production area regarding all the manufacturing and packaging process.To be in charge of sampling and generation of test request of in-process samples & finished products.

Responsible for assisting to establish, follow, and continuously improve quality system of GMP in company.Responsible for the implementation of GMP in company and staffs training with GMP.Grasp the related production technology, parameters and operational procedures. Responsible for the investigation of in-process deviation.