Assistant Manager - Packing

To handle the cytotoxic waste generated in the area and control the area in case of spillage.

To operate the cold room as per the SOP and ensure the temperature monitoring is done on regular basis as required.

To perform and ensure line clearance in the area are done before and after every stage of operation as per SOP.

To record the temperature as defined in the SOP.

To do and ensure status labelling in the area at each stage of activity.

To monitor temperature in visual inspection, leak testing, packing area and cold rooms are performed as per the SOP.

To perform and ensure material movement in the area as per procedure.

To perform the operation related Activity in eBRM.

To perform and ensure Operation and cleaning of labelling, sleeving & auto checkweigher as per SOP.

To perform and ensure Operation of pharma code verification and track n trace equipments.

To perform and ensure Brite stock packing.

To perform and ensure Secondary packing operation procedure for different products & market as per BPR.

To record the temperature as defined in the SOP.

To perform and ensure Secondary packing operation procedure for Japan market as per BPR.

To perform and ensure that verification and calibration of balance are done as per the requirement.

To handle the activities related to material issuance and return between warehouse and packing area.

To ensure that sodium vapor lamp are replaced at a frequency defined in the SOP.

To prepare the eMPCR & eMPR

To operate zebra printer and scanner as per the SOP.

To ensure that verification is performed and any non-compliance are handled as per the SOP.

To understand the process of packaging and rejects identification to ensure qualitative packaging is being performed

To perform packing belt set up and finished goods transfer after batch packing.

Yearly Calculator Verification Performance

To performed the reprocess and rework as per SOP.

To handle the cytotoxic waste generated in the area and control the area in case of spillage.

To perform and ensure audit trail back up is performed as per the SOP at regular intervals.

To perform reconciliation and AQL in Staging area

To perform the Visual inspection of Irinotecan HCL Injection as per SOP.

To perform the time verification of Equipment as per SOP.

To perform and ensure GDP is followed at all stages of activity in the area

To follow the change room entry and exit procedure for visual inspection, leak testing and packing area.

To initiate and Execute CWO and BDIS as and when necessary

To ensure that initiation of ROAR form before start vender work.

To perform and ensure GDP is followed at all stages of activity in the area.

To initiate the request for Breakdown, calibration and preventive maintenance.

Ensure & participate in cEHS Training.

To perform the destruction of the GMP documents.

To perform SAP transactions for PR initiation, Process order creation, material transfer. Etc.

To follow the change room entry and exit procedure for visual inspection, leak testing and packing area

To prepare and review the alarm assessment.

To prepare and get approve SOP, MPR and other Controlled Documents

To perform the DMS activity

For preparation approval and issuance of Master Production and Control Record and Master Packing Record Master

To keep track for the required training and to update the training software (OLTIMS) with training data.

To track the training of vender and third party.