1 Opening(s)
5.0 Year(s) To 6.0 Year(s)
2.50 LPA TO 3.50 LPA
Your day-to-day tasks are likely to include:
Keeping in contact with existing customers in person and by phone
Making appointments with and meeting new customers
Agreeing sales, prices, contracts and payments
Meeting sales targets
Promoting new products and any special deals
Advising customers about delivery schedules and after-sales service
Recording orders and sending details to the sales ...
1 Opening(s)
0 To 4.0 Year(s)
1.00 LPA TO 5.00 LPA
Job Description : Job ResponsibilitiesDevelopment of Fuel Cell & Electric Veh icles.
Understanding of Functioning of Various Electrical Control Systems, ECU's, Electrical
& Electronic functions inside Electri c Vehicles & Fuel Cell Vehicles. . Experience in
Handling Proto Build Issues, Production Issues & Field Issues. Technical Support f
or resolving all E&E System Level ...
1 Opening(s)
0 To 3.0 Year(s)
1.00 LPA TO 5.00 LPA
Problem identification and troubleshooting a variety of difficult mechanical
problems with limited supervisionDefine, coordinate, perform, and document engineering test reports with
limited supervisionDevelop, design, or modify mechanical engineering layouts/schematics
and/or detailed drawings/specifications of difficult scopePerform engineering analysis of difficult scope with limited supervisionTechnically lead and/or execute engineering projects, including development
of key suppliers. Generate ...
1 Opening(s)
0 To 5.0 Year(s)
1.00 LPA TO 5.00 LPA
Job Description : Job ResponsibilitiesDevelopment of Fuel Cell & Electric Veh icles. Understanding
of Functioning of Various Electrical Control Systems, ECU's, Electrical & Electronic functions inside
Electri c Vehicles & Fuel Cell Vehicles. . Experience in Handling Proto Build Issues, Production Issues
& Field Issues. Technical Support f or resolving all E&E System ...
1 Opening(s)
5.0 Year(s) To 7.0 Year(s)
4.20 LPA TO 4.60 LPA
JOB DESCRIPTION
Quality Engineer
Male
1
5 to 7
B.Tech / B.E Mechanical
Roles and Responsibilities.
Ensure safe working condition of all employees. If any unsafe activity observed immediately contact with production head and safety head.
2.To check all production as per standard.
of the product should be as per quality requirement.
To test daily production as per lab testing ...
1 Opening(s)
2.0 Year(s) To 7.0 Year(s)
6.00 LPA TO 8.00 LPA
· Responsible for achievement of the sales target (actual vs target) across the sales category. Monitor sales against agreed targets on a regular basis to ensure they are met and where necessary the need for remedial actions are identified, reported and implemented
· Ensure timely collection of the agreed commercials from ...
1 Opening(s)
0 To 5.0 Year(s)
1.00 LPA TO 5.00 LPA
Responsible for: . Analyzing, collecting data, and providing accurate, documented information
about the status of quality . Verifying the correctness of quality related development results in
compliance with the Quality Management Plan & authorize their release for medical devices .
Validation of compliance to basic requirements, e.g. ISO standards and regulations like Medical
Device ...
1 Opening(s)
0 To 2.0 Year(s)
1.00 LPA TO 2.00 LPA
Responsible for: . Analyzing, collecting data, and providing accurate, documented information
about the status of quality . Verifying the correctness of quality related development results i
n compliance with the Quality Management Plan & authorize their release for medical devices
Validation of compliance to basic requirements, e.g. ISO standards and regulations like Medical
Device ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 5.00 LPA
Position Designation - In-Charge Capcell Plant
Grade - Executive E1
5 years as Incharge of production department in any rubber or Eva production unit .
Hands-on experience for Rubber Mixing plant and product testing will be preferred.
Must have knowledge in ISO/OSHAS/5S & SAP activity.
Degree in Mechanical or Chemical engineering, preference will be given ...
1 Opening(s)
0 To 4.0 Year(s)
1.00 LPA TO 3.00 LPA
Responsible for: . Analyzing, collecting data, and providing accurate,
documented information about the status of quality . Verifying the c
orrectness of quality related development results in compliance with
the Quality Management Plan & authorize their release for medical devices
. Validation of compliance to basic requirements, e.g. ISO standards and
regulations like Medical Device ...