- Coordinate with the Sending Unit/ partner for new products and/or product development.- Create protocols and reports that are relevant to the needs of validation, verification, and each project plan.- Create URS for equipment.- Monitor the stock of materials, reagents and consumables; and obtain the appropriate items, especially for the purposes of validation, verification, and each project plan.- Manage and schedule the activities of the analysts according to the project, in coordination with the QC supervisor (routinely).- Oversee general laboratory activities, including compliance, laboratory practices, and nonconformances found in laboratory areas.

Focus on :1. Method development and validation of Nitrosamine Impurities listed by FDA/HSA/etc in drug substance and drug product also by LC-MS/MS, LC-HRMS, GC-MS, GC-MS/MS, GC-HRMS (APGC)2. Method development and validation of AZB impurities (e.g AZBT) in sartan groups by LC-MS/MS3. Responsible to develop analytical method for finished product and raw material for NPD and EPI to perform ISS sample lab trial, SCU, and PSC4. Impurity profiling of pharmaceutical products and raw materials to determination about unknown impurity by HRMS Instrument5. Perform reverse engineering6. Prepare documents for registration of pharmaceutical products7. Perform analytical method transfer to manufacturing site

Join research group : Peptide synthesisTotal synthesis of cyclodepsipeptide aureobasidin-L using solid- and liquid-phase peptide synthesis as main topic for thesis project