Department:
Production – CAPSULE
Experience:
7 Years
Education:
B .PHARM, Capsule FDA approved
Responsibilities:
- GMP & c GMP- to be followed in capsule production area.
- To maintain departmental & equipment cleanness, Daily follow up for RM & PM
- Allocation of manpower at all works station.
- To put all record update & online documentation on daily basis
- Co-relation of OEE of equipments, daily output analysis and performance on monthly basis. To train Executives & Officer & Operators.
- Optimum utilization of equipment and control various breakdown, Hazardous waste at each stage of process.
- Machine loading as per production plan on monthly basis and day wise schedule preparation
- To be complete monthly plan by 99%
- To updating Oracle entries, FG reports & monthly closure in oracle system, To give BMR & BPR requisition to Q.A
- To Co-ordinate with other department.
- Generation of Barcode Label and its related documents.
- Monthly stereos ordering as per production plan and its reconciliations and area up keeping.
- Handling of shift works in capsule department.
- To give dispensing plan to store department.
- To prepare shift scheduled at every week.
- Oracle updating & MIS reporting.
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