• I have successfully completed my probation period regarding quality control analysis specifically for HPLC and GC for method development, method validation, calibration, Protocol & Report generation.
• My key responsibilities at this position include, but are not limited to -
? Conduct routine and advanced analytical tests, Method development, Method validation using HPLC, RRLC, GC, UV Spectroscopy, Wet Analytical techniques in accordance with BP methodologies (for our U.K Client), ICH Guidelines[Q2(R1)], cGMP, GLP, FDA regulations and, 21CFR p11.
? Write Protocols/MOA, Reports, Methods, Standard operation procedures and submission documents.
? Analyze analytical data, identify trends and provide recommendations.
? Conduct instrument troubleshooting & Calibration.
? Train students for HPLC, GC & and Advance Chromatography.