Posted:2 months ago|
Platform:
Work from Office
Full Time
Develop new methods for the Nitrosoamines, Genotoxic impurities and perform method validation. Responsible for LC/MS analysis of samples. Prepare method development report, STP, Method validation protocol, method validation report and sample analysis report. She/he shall be supporting routine mass analysis and Impurity profiling (LC-MS) with documentation as per GDP. She/he shall be able to do literature search on latest technology. Thorough knowledge of latest guidelines. Perform calibration of instruments as per SOP.
Apitoria Pharma
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