Details: Summary: P erforms analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing and may also work on method development/method validation projects. The key techniques utilized are LC/MS and/or GC/MS analysis. Typical types of testing include structure elucidation and characterization using mass spectrometry; quantitative analysis using LC/MS and/or GC/MS; trace analysis using LC/MS and/or GC/MS. Maintains professional expertise through the familiarity with scientific literature and use professional concepts to contribute to the development of company concepts and principles and to achieve objectives in creative and effective ways. Will also exercise independent judgment in developing methods, techniques and evaluation criteria for obtaining results; write client reports and protocols; interact with clients and participate in FDA and/or client audits. Qualifications: BS degree in Chemistry or related science with 10+ years working experience in drug analysis field or MS with 3+ year of related experience. Must be experienced in chromatography and chromatography hyphenated with mass spectrometry (i.e. HPLC, GC, LC/MS, GC/MS). Experience in other spectroscopic techniques (i.e. UV, IR, NMR) would be considered a plus. A strong knowledge of GLP/GMP policies and regulations is also required. Position also requires detailed understanding of the theoretical basis of the methods/experiments along with ability to troubleshoot equipment; ability to efficiently organize the routine work with minimum supervision; and ability to properly evaluate and interpret generated data.