Executive

Compilation and Review of all types of data of the products analyzed at each stage (RM, PM, FG, Stability and GLP documents).

Responsible for Review of Calibration and Audit Trials Verification.

Responsible for assuring all Laboratory activity are carried out in compliance with existing SOP.

Responsible for Integration of HPLC and GC data and new Method Creation.

Verification of chemicals, volumetric solutions and reagents in LIMS.

Preparation of LIMS protocols for testing of RM,PM and FG Testing and release.