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 ...
1 Opening(s)
0 To 2.0 Year(s)
1.00 LPA TO 8.00 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 Regulation ...
1 Opening(s)
0 To 3.0 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 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 ...
1 Opening(s)
0 To 1.0 Year(s)
1.00 LPA TO 2.00 LPA
testing new processescollecting data required to make improvements and modificationsoverseeing the construction of new plantsusing and developing process simulation software to work out the best production methodspurchasing and installing equipmentusing scientific principles related to magnitude, momentum, heat transfer etcsupervising plant operationsinvestigating and troubleshooting plant/process problemsscheduling and coordinating work to tight ...
1 Opening(s)
2.0 Year(s) To 9.0 Year(s)
2.00 LPA TO 5.00 LPA
Responsible for: . Analyzing, collecting data, and providing accurate, documented information abou
t 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 ...
1 Opening(s)
10.0 Year(s) To 20.0 Year(s)
Not Disclosed by Recruiter
Ø Projection of market potential for current selected API market and for the new product
Ø Hands on experience in handling around 150- 200 Cr Domestic Market
Ø Capable of identifying new business/ customers for existing market and even for the new products .
Ø Arranging trade shows, fairs, coordinating with organizer stall ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 3.50 LPA
We are searching for a reliable, innovative production engineer to oversee Chemical processes company at Jagdalpur.
testing new processes
collecting data required to make improvements and modifications
overseeing the construction of new plants
using and developing process simulation software to work out the best production methods
purchasing and installing equipment
using scientific principles related to magnitude, ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
1.80 LPA TO 2.40 LPA
Duties
Analyzing work orders, engineering plans, specifications, and blueprints to plan machining
Interpreting GD&T (Geometric Dimensions & Tolerances)
Writing and interpreting CNC machine language/programming
Setting up lathes and creating setup instructions
Creating tooling fixtures for prototypes
Partnering with Engineering on tooling design, process improvements, and product introduction
Verifying settings inspecting, and submitting first article to quality department
Collecting ...