Analytical Chemist III
Solvias Group
Position Overview Requires supervisory and/or technical experience. Responsible for overall direction and completion of analytical studies. Develop new methodology and novel approaches to problem solving for analysis of trace constituents in test materials for pharmaceutical applications. Responsible for method transfer in a coherent manner while adhering to appropriate regulatory requirements, including SOP’s, Protocols, US FDA Good Laboratory Practices (GLP) current Good Manufacturing Practices (cGMP). Critical Performance Areas Develop new methodology for analysis of drug substance and drug products in support of Contract Analytical Programs. Responsible for overall direction and completion of studies. Accurately record and document raw data, observations and pharmacy usage. Ensure that work conforms to appropriate regulatory requirements, including SOP’s, Protocols, US FDA Good Laboratory Practices (GLP), US FDA current Good Manufacturing Practices (cGMP), ICH and USP guidance. #J-18808-Ljbffr Solvias Group
Vacancy posted 1 day ago
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