Analysis of samples as per existing release specifications 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
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Thanks,
Kamal
Keyskills: Failure investigation change control documents and reviewing of related corrective and preventive activities.