1 Opening(s)
6.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 9.00 LPA
JD cum Key words for Profile : -
Knowledge about ISO 9001; 14001 & 45001 & face ISO audit in previous company.
Knowledge about NABL (ISO/IEC 17025:2017) & face NABL audit in previous company.
Prepare SOP, Procedure, require format & link with QMS / Manual.
Knowledge about supplier management system & customer complaint ...
1 Opening(s)
0 To 1.0 Year(s)
1.00 LPA TO 2.00 LPA
Responsibilitiesof the QA Engineer will include:-Participate in the full Information Technology project lifecycle withparticular emphasis on Quality Assurance activities in the properimplementation of the Information Technology projects.-Responsible for supporting the development of comprehensive test strategies,plans, reports and environments for manual or automated testing for multiple ITprojects in a release cycle.-Responsible ...
1 Opening(s)
0 To 2.0 Year(s)
1.00 LPA TO 4.00 LPA
Responsibilitiesof the QA Engineer will include:-Participate in the full Information Technology project lifecycle withparticular emphasis on Quality
Assurance activities in the properimplementation of the Information Technology projects.and
environments for manual or automated testing for multiple ITprojects in a release cycle.
-Responsible for understanding the complex software architecture, softwaredesign documents,
software quality assurance complexity and ...
1 Opening(s)
0 To 1.0 Year(s)
1.00 LPA TO 4.00 LPA
Participate in the full Information Technology project lifecycle withparticular emphasison
Quality Assurance activities in the properimplementation of the Information Technology projects.-Responsible for supporting the development of comprehensive test strategies,plans, reports and
environments for manual or automated testing for multiple ITprojects in a release cycle.-Responsible for understanding the complex software architecture, softwaredesign documents
, ...
1 Opening(s)
0 To 2.0 Year(s)
2.00 LPA TO 4.00 LPA
Responsibilitiesof the QA Engineer will include:-Participate in the full Information Technology project lifecycle withparticular emphasis on
Quality Assurance activities in the properimplementation of the Information Technology projects.-Responsible for supporting the development of comprehensive test strategies,plans, reports and
environments for manual or automated testing for multiple ITprojects in a release cycle.-Responsible for understanding ...
1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
7.00 LPA TO 12.00 LPA
? To assist in developing & implementing various quality control tests like HighVoltage, Partial Discharge, tracking and erosion test, Tensile & ultimateelongation, Hot elongation, Dielectric strength.? Preparing & maintaining various audit & Inspection reports like OHSAH & ISO.? Handling customer needs and requirements to develop effective QC process? Ensure incoming ...
1 Opening(s)
0 To 2.0 Year(s)
2.00 LPA TO 4.00 LPA
Manage the Quality Control/Quality Assurance including but not limited to: lot management
, stability review, temperature monitoring, maintenance of quality agreements, release of products
for
anage the Quality Control/Quality Assurance including but not limited to: lot management
, stability review, temperature monitoring, maintenance of quality agreements, release of products
for sale, product inspection (audits) and ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
1.00 LPA TO 2.00 LPA
eeting with the product design team to determine product testing parameters.
Writing test plans and creating test cases for the product.
Conducting quality assurance and designing performance tests using the new testing procedures.
Troubleshooting any errors and streamlining the testing procedures.
Writing up the final QA and test procedures for the quality technicians.
Training the ...
1 Opening(s)
0 To 2.0 Year(s)
4.00 LPA TO 8.00 LPA
Quality Engineer Standards and Regulations Good knowledge of the relevant Standards/Regulations for medical device manufacturers (ISO 13485, ISO 14971
, MDD, MDR, 510(k) etc.) Ensuring compliance of products as per MI PLM and SHPL QMS requirements Co-ordination with Quality Assurance Manager on various
SHPL QMS related activities Conducting/participating in Internal Audits and ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 5.00 LPA
Quality Engineer Standards and Regulations Good knowledge of the relevant Standards/Regulations for medical device manufacturers
(ISO 13485, ISO 14971, MDD, MDR, 510(k) etc.) Ensuring compliance of products as per MI PLM and SHPL QMS requirements Co-ordination
with Quality Assurance Manager on various SHPL QMS related activities Conducting/participating in Internal Audits and External ...