Posted:4 weeks ago| Platform:
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Full Time
QA & IATF Documentation, CAPA Analysis, SPC, MSA, Control Plan, FMEA, MDR Requirement, Cleanroom Validation, Calibration Work, Lab equipment handling, Rheo logy, Visco matter, VTM, Develop and Implement QA Processes
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2.0 - 5.0 Lacs P.A.
16.0 - 18.0 Lacs P.A.
1.0 - 4.0 Lacs P.A.
3.0 - 7.0 Lacs P.A.
4.0 - 8.0 Lacs P.A.
5.0 - 6.0 Lacs P.A.
7.0 - 9.0 Lacs P.A.
3.75 - 6.0 Lacs P.A.
4.0 - 5.5 Lacs P.A.
2.0 - 4.0 Lacs P.A.