JOB OVERVIEW: The role entails providing remote support for the Quality Management System (QMS) and reviewing microbiology data for Piramal Pharma Limited (PPL) sites. Key responsibilities include overseeing Out of Specification (OOS) investigations, laboratory incidents, deviations, and change controls, as well as reviewing data generated in the microbiology laboratory. Additional duties involve drafting and reviewing documentation, ensuring adherence to regulatory standards, and recommending ongoing 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)