Job Description
1:Documentation handling and preparation of Change Control, Deviation, OOS, CAPA,Lab incident, APQR and investigation, follow up for the closure of the same.
2:Handling of Cell Bank Documents and Technology Transfer Documents.
3:Review of Process validation protocol and report , Review of Cleaning Validation protocol and report, Batch records,
4:Review of CPV data,
5:IPQA shop floors investigation.
1: Handling of JMP software for CPV and PQR,
2: Execute and monitor the Internal Audit programs to maintain the Good Manufacturing practices within the organization.
3: Management of QA team it engagements.
