1 Opening(s)
4.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 5.00 LPA
toys to give a unique and delightful experience to kids. We primarily focus on advanced technology and processdriven manufacturing to give the best quality experience to our customers. We have an immediate opening for therole of QC Engineer. The QC Engineer is responsible to check the incoming goods, do in ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: Process Officer
Location: Vapi
Experience: 3- 5 Years
Industry: Pharma - API
Responsibilities:
Process design engineering (Basic, detailing & Improvement)
Preparation of Material balance, PFDs, heat balance, and capacity calculations for a product.
Preparation & review of P&IDs as per standards. Generate documents for design projects ...
1 Opening(s)
7.0 Year(s) To 8.0 Year(s)
7.00 LPA TO 9.00 LPA
Description:
Position: Sr. Executive - QA
Location: Bhimpore - Daman
Experience: 7 - 8 YEARS
Industries: Pharma
Responsibilities:
Issuance & Control of all Quality Documents Deviation control, change control, Investigation of OOS, Specification, SOP, and BMR.
Assist to head in ensure the evaluation of ...
10 Opening(s)
2.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
Department: ProductionDesignation: Operator/Semi-OperatorQualification: ITI AOCP (Chemical)Experience: 2 to 5 Years Experience in the Grain Bashed Food IndustryLocation: Jhagadia, Bharuch (Gujarat)Job Description: Preferred Good exposure on Unit Operation & Unit Process, Safety, ChemicalHandling, and Equipment handling like Pumps, SS reactors, Vacuum Pumps, IonExchange, etc. Should have strong experience in any unit ...
3 Opening(s)
1.0 Year(s) To 2.0 Year(s)
1.00 LPA TO 1.80 LPA
Urgent Hiring for Shift Chemist for PharmaLocation - IndoreResponsibilities:-
Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures.
Monitor and control chemical processes during production to ensure consistency and quality of pharmaceutical products.
Collect and prepare samples from different stages of production for analysis.
Maintain accurate and detailed ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
3.60 LPA TO 5.40 LPA
Job Description:1. Responsible for Overall QA activities & to look after QMS compliance in accordance with ISO 13485/cGMP.2. Preparation & Up-gradation of SOP, Specifications3. Maintain the Records of BMR, BPR, Batch Inspection Documents4. Maintaining Document & Record Control5. Preparation & Up-gradation of Routine Validation Protocol & Reports.6. Handling CAPA, Non- ...
3 Opening(s)
2.0 Year(s) To 4.0 Year(s)
2.50 LPA TO 3.60 LPA
Position: Shift Incharge - Production
Location: Ankleshwer
Experience: 2 - 4 Years
Industries: Chemical
Responsibilities:
Managing the shift activities and manpower’s involved in the production activities.
Handling the Operational and Chemical reaction batch, handling the hazardous chemicals and various operational equipment’s like vacuum distillation, distillation and extraction.
Responsible for planning and execution of Monthly production schedules.
Prepare production plan and to co-ordinate production manager.
Documentations of production records as per ISO 9001,14001 & 45000 requirements.
Optimize the usage of ...
2 Opening(s)
0 To 3.0 Year(s)
1.20 LPA TO 1.60 LPA
Description:
Computer Operator Job Responsibilities:
Provides data by operating a computer.
Determines sequence of operations by studying production schedule.
Performs defined tasks per documented instructions/processes.
Prepares equipment for operations by accessing software in computer.
Makes appropriate changes to the documentation, as needed.
Monitors and manipulates daily system jobs.
Starts operations by entering commands.
Maintains operations by monitoring error and ...
1 Opening(s)
6.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 7.00 LPA
Job Overview -
Routine Microbial Analysis of Raw Material & Finish Good Samples
Routine Calibration
Environment Monitoring
Media preparation
Product Stability
Documentation
Report Preparation
Responsibilities and Duties-
- Work planning and distribution to team members
- Prepare monthly, quarterly and annual sampling plan, Validation plan and/or qualification plan
- Prepare and implement stability plan for all products.
- Daily Reporting and release ...
3 Opening(s)
1.0 Year(s) To 6.0 Year(s)
1.00 LPA TO 6.00 LPA
Should understand and follow the chemical manufacturing process.He should follow the SOP strictly. To check and confirm all the required raw materials are available before starting the batch.Able to handle unskilled workers and get the work done.Able to understand technical problems in the manufacturing line and trouble shooting.Should have computer ...