Titan Laboratories Ltd - Walk-Ins for Multiple Positions - QC / QA / Production on 11th & 12th Jan' 2020
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Time: 11:00 to 4:00 pm
Experience: 2-7 yrs
Job 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
Walk -In Officer / Executive -Quality Control @ Mahad
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Finished Formulation
Time: 11:00 am to 4:00 pm
Note: Same day selection kindly carries Salary Documents
2 - 8 Years Experience Must- (Only Male candidate Preferred
Pharma Background)
Openings: 20
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.
Walk IN Production Executive (Finished Formulation) @ Mahad
Walk In Interview Same day offer if selected
Experience: 3-7 yrs
Openings: 09
Time: 11:00 am to 4:00 pm
Job Responsibilities:
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.
Date & Time: 11th January - 12th January , 11 AM onwards
Venue:
EU- GMP, Certified, Plot No. E27/1 E27/2, MIDC.
Mahad, Village -Jite, Dist. Raigad Titan Laboratories Pvt Ltd
Contact - Shivali Khanna ( HR)
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