1 Opening(s)
0 To 5.0 Year(s)
1.00 LPA TO 2.00 LPA
Facilitates the execution of the QA strategy through
leadership, operations teams and support teamsIntroduces new systems and procedures that drive defect
identification and reductionVerifies quality metrics in place and triggers containment
actions and corrective actions as necessaryCommunicates across all levels on quality operations and
programs progressLeads root cause analysis and error trend analysis, and
provides ...
1 Opening(s)
6.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
CMM-CALYSPO (Windows based software used in 3Dco-ordinate measurement m/c for inspection) Uses Roughness tester Mahr model, Used to measurement of surface roughness parameters and Counter parameters of components of Engine parts
Monitoring and controlling of receipt material inspection (Machining, casting, Sheet metal, Molding & Rubber components) and also approved the inspection ...
1 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 10.00 LPA
Responsible for implementation of all QA/QC procedures in site
Setting up Quality Control Laboratory as per the contractual requirement.
Maintaining ITP and all other Quality Assurance/Quality Control related Inspection reports.
Conducting Internal audits, preparing audit reports and follow up for CAPA
Conducting Tests on Aggregate, Soil, Cement, Concrete etc... As per the approved ITP.
Conducting ...
1 Opening(s)
0 To 5.0 Year(s)
1.00 LPA TO 4.00 LPA
Are you looking at developing future leaders Come join us at Siemens. Siemens Global Business
Services (GBS) is a Siemens Service Company that provides innovative digital solutions and customer
-oriented business services. With more than 20 years of experience, Siemens GBS taps into its
understanding of how organizations and businesses work to seamlessly ...
2 Opening(s)
2.0 Year(s) To 8.0 Year(s)
0.00 LPA TO 0.00 LPA
We are having an urgent opening for the position of Quality Executive for a reputed company at the Taloja/ Murbad location.
Job Description:
Must have at least 2 years of experience as a Quality Executive.
Must have key expertise in Quality analysis.
Experience in chair/furniture/ plastic/sheet Metal and plastic is preferred.
Must have good experience in Quality analysis and handling ...
1 Opening(s)
0 To 4.0 Year(s)
1.00 LPA TO 5.00 LPA
Quality is everything at Dell Technologies. It's what we're known for and
we build it into all our processes. In Quality Engineering we play a central
role by developing, implementing as well as maintaining technical quality a
ssurance and control systems. We look for ways to improve the inspection,
verification and validation of our ...
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)
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)
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 ...