Titan Laboratories Pvt. Ltd Walk-In Interview @ Mahad, Production, Quality Control, Quality Assurance 19th January 2020
Walk-In
Interview @ Mahad, Production, Quality Control, Quality Assurance
Only Male
Candidate need to Apply for All the Position
Kindly Carry
Salary Documents
Venue:
Titan
Laboratories Pvt. Ltd
Time: 11:00
to 4:00 pm
Date: 19th
January, 11 AM onwards
EU- GMP,
Certified, Plot No. E27/1 E27/2, MIDC. Mahad, Village -Jite, Dist. Raigad
Quality
Assurance
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
Quality
Control
1. HPLC 21
CFR Compliance System Handle
2. Instrument
handling like, HPLC / Dissolution / UV / IR / GC etc.
3. Maintain
the Reserve samples and their quality review.
4. Handling
of General SOP's and Operating procedures of Analytical Instruments,
Calibrations of Instruments.
5. To
maintain documents as per EUGMP, WHO-GMP, c GMP. MHRA, USFDA, TGA, TPD etc.
6. Candidate
should have good understanding of subject matter.
7. Candidate
should face the audit like EUGMP, MHRA, USDFA, TGA etc
8. Candidate
Should have good communication skills. Production
1.
Responsible for Operation and cleaning of Extruder and spheronizer, Tray dryer,
Coating Pan
2.
Responsible for granulation activity, Operation and cleaning of RMG, FBD,
Multimill.
3.
Responsible for NPS coating, Operation and cleaning of FBE (Top spray/Bottom
Spray)
4.
Responsible for Compression of Tablets, having a sound knowledge of single and
Bilayer tablet, Operation and cleaning of Cadmach, Cadpress machine 37 stn and
49 stn, Knowledge of PLC.
5.
Responsible for Coating of Tablets, Having Knowledge of Autocoater, Coating of
Film coating, Sugar Coating, Enteric coating, Knowledge of PLC.
6. Cleaning
and sanitization activity
7. Regular
inprocess and daily work execution
8.
Responsible for filling of daily entries of area cleaning, BMR, Temperature
Humidity.
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