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