JOB OVERVIEW: 

The role involves providing remote Quality Management System (QMS) support to Piramal Pharma Limited (PPL) sites, focusing on the management of OOS investigations, laboratory incidents, deviations, and change controls. Responsibilities include drafting and reviewing documentation, ensuring compliance with regulatory standards, and recommending continuous improvements.

 

KEY STAKEHOLDERS: INTERNAL – Site Quality Team (QC, QA), Corporate Functions

 

EXTERNAL – Regulators (during inspection), Solution Providers

 

REPORTING STRUCTURE: PPL Site Quality (Functionally) and CQA Document, Data Review & Creation

(Administratively)