Walk In Interview QA
Time: 11:00 to 4:00 pm
1) Asst Manager - 2 Position - Reviewer / Team Handling
exp: 7 to 10 yrs
Qualification : B Pharm
2) Executive: 5 Position - Reviewer
Exp: 4 to 7 yrs
Qualification: B pharm
3)Officer/ Sr. Officer- 7 Position
Exp: 2 to 4 yrs
Qualification: B pharm
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Responsibility
Responsible for Implementation and ensuring of the process is compliance with BMR, SOPs,
GDP Implementation.
Responsible for Handling, Monitoring, Planning and execution of activities related of IPQA
shop floor activities (Dispensing, Granulation, Blending, Compression, Capsule filling, Coating
and Inspection).
Responsible for giving Line clearance from Product to Product & Batch to Batch change over
according to standard operating procedures for start of various Manufacturing Operations
Responsible for Verification of Allocated Expiry date.
Responsible for performing in-process checks.
Responsible for Calibration of IPQA Instruments.
Responsible for performing AQL (Acceptable Quality Limit) for Tablets and capsules after
completion of batch.
Responsible for execution of process validation, cleaning validation, Equipment validation, Hold
time study and stability study as per the protocol.
Responsible for execution of sampling at all stages as per process validation, cleaning validation,
To collect the Swab samples for Chemical & Detergent as per the sampling plan.
Ensure that Assay Calculation at dispensing stage and ensuring that the materials are dispensed
as per the standard quantities mentioned in the BMR.
Responsible for Yield calculations at different stages of manufacturing to ensure process loss
with respect to each stage.
Responsible for review of Quality records of Engineering, Warehouse & Production
records.
Responsible for Preparation and review of SOPs, BMRs, Protocols.
Responsible for review of Batch manufacturing record.
Responsible for dispatch the final packed product to respective market.
Responsible for handling of deviation and change control.
Responsible for handling of Equipment Performance Qualification, Breakdowns and PMP.
Coordinate effectively with Manufacturing, Store, QA, QC and Engineering departments
Responsible for Implementation and ensuring of the process is compliance with BMR, SOPs,
GDP Implementation.
Responsible for Handling, Monitoring, Planning and execution of activities related of IPQA
shop floor activities (Dispensing, Granulation, Blending, Compression, Capsule filling, Coating
and Inspection).
Responsible for giving Line clearance from Product to Product & Batch to Batch change over
according to standard operating procedures for start of various Manufacturing Operations
Responsible for Verification of Allocated Expiry date.
Responsible for performing in-process checks.
Responsible for Calibration of IPQA Instruments.
Responsible for performing AQL (Acceptable Quality Limit) for Tablets and capsules after
completion of batch.
Responsible for execution of process validation, cleaning validation, Equipment validation, Hold
time study and stability study as per the protocol.
Responsible for execution of sampling at all stages as per process validation, cleaning validation,
To collect the Swab samples for Chemical & Detergent as per the sampling plan.
Ensure that Assay Calculation at dispensing stage and ensuring that the materials are dispensed
as per the standard quantities mentioned in the BMR.
Responsible for Yield calculations at different stages of manufacturing to ensure process loss
with respect to each stage.
Responsible for review of Quality records of Engineering, Warehouse & Production
records.
Responsible for Preparation and review of SOPs, BMRs, Protocols.
Responsible for review of Batch manufacturing record.
Responsible for dispatch the final packed product to respective market.
Responsible for handling of deviation and change control.
Responsible for handling of Equipment Performance Qualification, Breakdowns and PMP.
Coordinate effectively with Manufacturing, Store, QA, QC and Engineering departments
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