PhD chemist with extensive experience in analytical method development and QC for modified oligonucleotides and their precursors. My expertise includes operating and troubleshooting LC-MS and HPLC systems for in-process and final product analysis. I have a strong background in developing and optimizing methods for a variety of analytes using techniques such as RP-HPLC, AEX-FPLC, and LC-MS, directly supporting the characterization of nucleic acid therapeutics. Familiarity with cGMP environments and developing and validating HPLC test methods in accordance to USP and ICH guidelines.
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