05 Aug
|
Coral Drugs
|
India
Posted:
March 2026
Role & Responsibility:-
Compilation of Supporting documents for Change Control/Deviation/CAPA/OOS.
Handling & Investigation of OOS
Preparation & Review of SOP’s.
Handling customer Complaints
Handling Change Control, Deviation , CAPA,OOS.
Responsible for Document Archival & up keeping. Preparation of Certificate of Analysis for Dispatch as per Sale order.
To work & implement the cGMP practices in to all departments as per SOPs.
Preparation of SOPs & relative documents.
📌 Executive - Quality Assurance (India)
🏢 Coral Drugs
📍 India