Scientist - Method Development

Method Development Associate Scientist/Scientist Essential Responsibilities Develop and validate HPLC procedures for small molecule drug substances and drug products. Perform forced degradation studies and develop stability-indicating assay and impurities methods Work in a GLP/GMP laboratory. Coordinate the timely and compliant generation of data to support client projects. Perform routine HPLC, GC, NMR, MS, IR, ICP, KF and other analysis and validation studies. Author and review protocols and reports. Review data for technical content and accuracy. Maintain current expertise with relevant ICH, GMP, and FDA guidelines. Requirements Educational Qualifications B.S. to Ph.D. in Chemistry or related field with 5+ years analytical laboratory experience or equivalent combination of education and experience is required. Relevant experience in good manufacturing practices (GMP) laboratory is required. Specific Skills and Requirements Experience with standard lab instrumentation (HPLC, UPLC, etc.) Experience with LCMS and GC preferred but not required. Be proficient Microsoft Excel and Word Must have basic knowledge chemicals their properties, structure, reactivity, and be able to handle with safe and appropriate techniques. Must have basic knowledge of arithmetic, algebra, and statistics. Must be able to communicate effectively with all plant and office personnel. Must be able to effectively multi task PId0890e0f2b23-29... PDN-9ef7f130-a7c4-4a2f-a43e-14021838aa4b