
Packaging Supervisor with 5.5 years of experience in pharmaceutical manufacturing, skilled in managing packaging operations under cGMP and according to SOPs. Proven ability to lead teams, optimize packaging processes, and ensure compliance with quality. Strong expertise in coordinating production schedules, training staff.
Packing Operation:
Additional Responsibilities:
Data acquisition system: material consumption during batch packing,additional MRQN data, yield data, shorting data.
Rejection data: analysed rejection data of executed batches for rejection
control.
Alarm management: daily critical alarm tracking, weekly critical alarm tracking and six month critical alarm trending.
Electronically generated reports review: Audit trail, production summary reports of executed batches.
Qualification: Execution of qualification document
Logbook management: tracking of logbooks at shop floor, to insure that all required logbooks are available in shop floor to prevent downtime and maintain stock of logbook with communicate with vendor.
MES execution ( EBPR)
Complete guide to process validation in pharma manufacturing ( From : Udemy )
Complete guide to process validation in pharma manufacturing ( From : Udemy )