Production and Packing planning, Monitoring and reporting daily Production Activities, Master Creation In Pharma Cloud, SAP. IPQA, Document Issuance & Control, CSV, Stability, Validation
Analyst Finished, Stability Section, knowledge of Instrument - HPLC, GC. Preferably know-how of Chromele on Software. Require good exposure in Lab QA related work. D.Pharma / B.Pharma / M.Pharma
Downstream and Upstream Manufacturing Mammalian and Microbial, QMS; DP Medical Device, Packing and Visual Inspection Labelling, Cartoning, Pick and Place Robotic Machines Handling and Track and Trace; DP and DS Engineering, Maintenance Automation, Instrumentation, Injectable Maintenance, QMS; M.Pharm, B.Pharm, MSc Chemistry, Biotechnology, Life science, Microbiology