To put all record and manufacturing area update & online documentation on daily basis
Co-relation of daily production report of equipment’s, daily output analysis and performance on monthly basis.
To train Operators, and contract man power
Optimum utilization of equipment and control various breakdown, hazardous waste at manufacturing stage.
Shift wise Volume Delivery in Mio at manufacturing stage.
To update ERP entries, FG reports & monthly closure in ERP system,
To give BMR requisition to Q.A and completed BMR review before submission.
To Co-ordinate with other department and handling of shift works in manufacturing department.
To give dispensing plan to warehouse department.
Calibration of equipment/instrument as per the define frequency
To maintain area cleanness and status labelling practices and all time audit readiness.
All statutory compliances adhered to FDA, Internal, CQA, Regulatory, EHS, and Audits etc.
Audit exposure - National Agency for Food and Drug Administration
and Control (NAFDAC) & other regulatory agencies. Adhere to other
compliance related to CQA, EHS and internal.
Exposure of IPQC instruments calibration & verification.
Rejection monitoring and action plan, online rejection completion.
Co-ordinate to engg for timely rectification of maintenance issues.
Change parts and spare management.
QMS activities - exposure of SOP writing, change control & deviation.
RM/PM availability check from warehouse & to give dispensing plan to warehouse.