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). Solvias is a global provider of chemistry, manufacturing, and control (CMC) analytics to the life sciences industry. Our expert team combines decades of experience with regulatory expertise across small molecules, biologics, and cell and gene therapies. Solvias offers end-to-end solutions from raw material testing to drug product release and API development for small molecules. Headquartered near Basel, Switzerland, Solvias operates six global Centers of Excellence, all adhering to the highest ISO, GMP, GLP, and FDA standards
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Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
Number of Employees
251-500 employees