To document, prepared the Quality as well as various technical documents & co ordinate approval from the Authorize Person as per the Policy of the company and in line with MDR& QMS Requirement.. To establish the Quality Management System in…
Finish goods release (Sterile) Environment monitoring Media stock maintain Clean room validation, Sterilization validation, ETO Validation, Gamma validation, sterile Barrier packaging validation etc…. Stability study Control sample preservation & monitoring (Sterile) BMR Review & Retention (Sterile) System Management as per…
1. In Process Check as per Quality plan as well as Specification 2. In Process Products non Conformity identify /raise the non conformity follow up for the closer 3. Line clearance 4. Codes /Labels /Packing Quantity of Product verification till…