Posted:-1 days ago|
Platform:
Work from Office
Full Time
Responsible for investigation of incidents, OOS, OOT, OOC & Deviation in Laboratory.
Responsible for Review and closure of investigation of incidents, OOS, OOT, OOC & Deviation in Laboratory.
Responsible for initiation & closure of Change Control, Deviations, CAPA in QEdge Software.
Responsible for Review of Standard Operating Procedures and Standard Test Procedures. Responsible for preparation of Protocols, Reports and Annexures Investigation & Documentation. Responsible for Review of analytical documents, and audit trials as per 21 CFR part 11 compliance.
Deep understanding of GMP, GLP, ISO 17025, regulatory guidelines, QMS, HPLC, GC, data integrity.
Intas
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