5 - 10 years
5 - 7 Lacs
Posted:1 day ago|
Platform:
Work from Office
Full Time
Analysis of samples as per existing release spe c ifi c ations and testing methods Ensuring strict adherence to Current Good Manufacturing Practice (cGMP) and Current Good Laboratory Practice (cGLP) to maintain high product quality Executing thorough investigation of Out of Specification (OOS), Out of Trend (OOT), and incidents, ensuring the implementation of appropriate Corrective and Preventive Actions (CAPA) when required. Playing a crucial role in Stability Management within Quality Control, including monitoring all stability-related activities and chambers. instrument HANDLED AUDIT FACED USFDA, EUGMP PLEASE SHARE YOUR UPDATED CV ON placement@balpharma.com Thanks, Kamal
Bal Pharma
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