1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
6.00 LPA TO 10.00 LPA
Leading and Management of IPQA team.Performing IPQA activity (Line clearance, in-process checks, sampling, etc.) at shop floor for Dispensing, Manufacturing, and Packing area.Review of executed Batch Processing Records and related cGMP documents for the on-time release of the batch.Preparation of SOP for execution on shop floor IPQA related activities.
Review of ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
2.10 LPA TO 3.60 LPA
Receiving Monthly & daily Production plan from Production Manager.
Manufacturing of batch as per MBR.
Temperature & Relative Humidity monitoring in manufacturing area.
Maintaining logbooks(General cleaning logbook,Equipment calibration & cleaning logbook,).
Preparation of daily production & manpower Record.
Online the Batch Manufacturing Record (BMR).
In process checks of all stages of manufacturing & packing of Tablet, ...
8 Opening(s)
0 To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Department - QA
Job Locaion - ambernath
Willingness should be there to work in all shifts
Job Description
Experience in issuing of line clearance at every step of Batch Manufacturing
Hands on performing In-process quality assurance checks for Tablets, Capsules and Intermediates.
Stability Sample Handling as well as Stability Chamber.
Monitoring and Executing Process Validation and Sampling of the same.
Carry out In-house Calibration and External Calibration of Balance, Instrument, Equipments, LAF and HVAC validation.
Periodic checking of Retention Sample and Handling of the same.
Documentation of Records.
BMR and BPR Preparation and reviewing.
Carry out Destruction Activities for Rejected and Expired Raw and Packing Materials.
Preparation of PQR & APQR.