Walk In Interview – Production, QA & QC
Department: Production
Required: 1 Production Executive
Required: 3 Production Officer
Required: rest will be operators
Experience: 4 - 7 yrs
Qualification: B.Pharm
Openings: 19
Job Responsibilities:
- Operation & cleaning tablet coating machine.
- Operation & cleaning of Compression
- On line entries of batch production record.
- Preparation of monthly as well as weekly production planning & yield report.
Granulation, Compression & Coating machine handled.
- Monitoring production activities.
- Palm Glatt, Wruster coater, FBE, FBC, Extrusion, Speronization and conventional pan loading machine handled.
- Preparation of production related documents & SOP.
- Review BMR.
- Writing Deviation, change control & whenever necessary.
- Maintain standard yield of all products.
- Stage wise production related entries done in SAP.
- Monitoring small scale R & D batches.
- Continuous training of production personnel to improve their competitiveness.
- Co-ordination with other departments.
Department: Quality Assurance
Required: 6 No Position
Exp: 4 - 10 Yrs
1) Validation- Required 1 (No)
2)QMS- Required 1 (No)
3)QA - Required 1 (No)
4)Microbiology- Required 1 (No)
5)IPQA - Required 1 (No)
6) Fresher - Required 1 (No)
Job Responsibilities:
- 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, Coatingand 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
1) Validation- Required 1 (No)
2)QMS- Required 1 (No)
3)QA - Required 1 (No)
4)Microbiology- Required 1 (No)
5)IPQA - Required 1 (No)
6) Fresher - Required 1 (No)
Job Responsibilities:
- 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, Coatingand 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
Department: Quality Control
Experience: 2 - 8 Years Experience Must- (Only Male candidate Preferred Pharma Background)
Responsibilities:
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.
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.
THE CANDIDATE MUST HAVE
1. Analytical Skills
2. Team Oriented
3. Good understanding of subject matter.
1. Analytical Skills
2. Team Oriented
3. Good understanding of subject matter.
Openings: 20
Location: Mahad
Date: 27th & 28th July 2019
Time: 10:00 am -4:00 pm
Venue:
Plot No. E27/1, E27/2, MIDC
Mahad, Village -Jite, Dist. Raigad
Titan Laboratories Pvt. Ltd
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