About the Role
We are hiring an Analytical R&D; qualified with hands-on experience in ICP-MS / ICP-OES for method development, validation, and elemental impurity testing. The role involves working in a cGMP-compliant environment with advanced analytical instruments.
Responsibilities
- Develop and validate analytical methods (ICP-MS / ICP-OES)
- Perform elemental impurity and routine analysis as per ICH Q3D
- Ensure GLP & cGMP compliance and accurate documentation
- Support method transfer and instrument troubleshooting
Requirements
- M.Sc. Chemistry (Analytical / Inorganic / General)
- 4-5 years of experience in Analytical R&D; (Pharma / Chemical industry)
- Hands-on with ICP-MS / ICP-OES; knowledge of HPLC, GC, UV, FTIR preferred
- Strong analytical, documentation & communication skill