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Elaborate and sign the certificates of analysis for API’s and excipients and submit them to the Sr. QC Supervisor to be released and signed.
Responsible for the qualification and calibrations of the lab. equipment. Also responsible for updating the list with all equipment’s
Provides plant/production support to assist manufacturing personnel resolving processing problems.
Performs all the activities detailed in the quality system procedures that are in conformity with the ISO 9001:2015 and cGMP Part II requirements
Train, direct, lead, and motivate QC staff to analyse raw materials and finished goods in conformance to specifications
Other duties as assigned
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