5 - 10 years
5 - 7 Lacs
Posted:2 months ago|
Platform:
Work from Office
Full Time
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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