Executive

GMP Documentation, Chemical Instrumental analysis, Capa, QC Finished goods stability, Lims, Glp

regulatory guidelines , capas , Cleaning Validation, Scale-up Knowledge, Process Validation, GMP SOPs, Computer Efficacy in MS-Office, Technical Risk Assessments, e-Residue Software Application, QMS Trackwise PACE, Product Development Process

Sap, Fmcg, Qms, Quality Monitoring, Gmp, Quality Control

analytical method validation , QMS activity, 21CFR Part 11, wet chemistry, Gmp, chromatography analysis, Glp

Ms Office, production reporting systems, herbal extraction, capsule manufacturing, GMP SOPs, Blending, Formulation, production documentation, Granulation, liquid production processes