18 Opening(s)
3.0 Year(s) To 4.0 Year(s)
1.90 LPA TO 2.70 LPA
Urgent Requiremet of Crane Operator for Reputed Steel plant at at Raipur Location .
Should be a crane operator & have driving licenses.Determine if any parts are malfunctioning.Operate crane under supervision.Manipulate or depress cane controls to regulate speed & direction of crane & hoist movement.Repair crane as needed.
Maintain all crane parts , safety pins , safety switches ,
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5 Opening(s)
7.0 Year(s) To 12.0 Year(s)
18.00 LPA TO 23.00 LPA
Responsibilities:
· Working Knowledge of all the BRM modules (Subscription Management, Billing & Invoicing, Payments & Account Receivable, Collections, Integration)
· Experience in understanding the requirement and translating that to functional and low-level design
· Must have worked as a BRM developer in their past and must be hands-on in BRM to verify the sanity of ...
3 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 5.00 LPA
To operate Inter Esterification operation.
To operate continuous bleacher system.
To minimize the down time.
To optimize the chemical & utility consumption.
To prioritize the safety measure and knowledge of hazards associated with sodium methoxide.
To maintain the quality parameters of processing
Monitoring of Deo OPRP monitoring.
TBHQ addition as per specification.
Process aids/ingredients management
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 12.00 LPA
Position: Manager/Asst. Manager - QA
Location: Silvassa
Experience: 8 - 10 YEARS
Industries: Pharma Formulation
Responsibilities:
To monitor and prepare budgetary provisions for procuring new QA equipment, upgrade the facility and smooth working of the department.
To release or reject all raw materials, intermediates, packing materials, ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.40 LPA TO 3.00 LPA
Position: QC Officer
Location: Silvassa
Experience: 2- 5 Years
Industries: Pharma- Formulation
Responsibilities:
Responsible for Documentation work in QC Department
Candidate must have knowledge of HPLC/GC.
Responsible for manufacturing the batch as per MOM or BMR.
Shall maintained all records related to manufacturing
Overall looking after the complete filling, packing activities and Procurement ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
1.80 LPA TO 3.60 LPA
Description:
Job Description of 2nd class Boiler Operator:
Responsible for operation of Boiler,Biomass boiler DM/Power Plant .WHRB Boiler including de-aerator operations Steam turbines and steam networksResponsible for safe shut down and start-up of boilers & boiler auxiliaries Handing over of equipment for maintenance & inspection and taking over after maintenance Issuance of ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 4.00 LPA
OPERATION RESPONSIBILITY ENSURE TURBINE OPERATION AS PER SOP OF TURBINE ENSURE HOUSEKEEPING ACTIVITIES AT TURBINE & SURROUNDING AREAS MAINTAIN LOG BOOKS ON SHIFT WISE & REPORT TO PLANT INCHARGE IF ANYVARIATION IN PARAMETER DURING TURBINE OPERATION. PHYSICAL CHECKS OF ALL RUNNING EQUIPMENTS DURING THE SHIFTS AT REGULARINTERVAL. ENSURE FOR SAFE ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: QA Officer
Location: Sarigam near by Vapi
Experience: 3 -5 Years
Industries: Pharma
Responsibilities:
To perform IPQA activities at shop floor in each and every stage of manufacturing and packing.
QA overview for clean room behavior and personnel hygiene .
Review of batch processing records.
Review of all ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
1.68 LPA TO 1.80 LPA
Description:
Roles & ResponsibilitiesOperate and control JCB equipment to ensure safe and efficient work. Perform routine maintenance checks on equipment to ensure proper functioning. Follow project plans and instructions to complete tasks efficiently. Ensure compliance with safety regulations and company policies.
Roles & ResponsibilitiesOperate and control JCB equipment to ensure safe and ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
2.00 LPA TO 4.00 LPA
Position: IPQA Officer
Location: Daman
Experience: 3 - 4 Years
Industries: Pharma
Responsibilities:
To perform IPQA activities at shop floor in each and every stage of manufacturing and packing.
QA overview for clean room behaviour and personnel hygiene .
Review of batch processing records.
Review of all documents relating to the manufacturing, ...