Job Title: Associate Scientist, QC Essential Responsibilities + Perform HPLC, GC, FTIR, KF, DSC, TGA, NMR, etc. + Inspect and perform complex chemical analyses on raw materials, in-process samples, and finished goods in accordance with cGMP/GLP standard operating procedures + May be able to perform routine ICP-MS and ICP-OES analysis for trace metals in a GMP analytical laboratory. + Coordinate raw material testing in a materials management system + Conduct inspections of manufacturing supplies + Conduct inspection of the laboratory or laboratory procedures to ensure conformance to internal quality system or external certification requirements and correct or eliminate process-related non-conformance items. + Dispose of expired retained samples and chemicals according to schedules and expiration dates in order to keep lab area clean and safe. + Experience with sampling raw materials and intermediates + Coordinate the timely and compliant generation of data to support client projects + Review data for technical content and good record keeping practices + Other duties as assigned Minimal Educational Qualifications B.S. in chemistry with a minimum of 3+ years or M.S with a minimum of 1+ year of related pharmaceutical analytical laboratory experience or equivalent combination of education and experience is required. Relevant experience in good laboratory/manufacturing practices (GLP/cGMP), laboratory quality control or stability, and interaction with quality assurance is required. Specific Skills and Requirements + Very strong experience with HPLC and GC + Experience with FTIR, TGA, DSC, NMR + Experience with XRD, IC, ICP-MS and ICP-OES a plus but not a must. + Experience with standard lab equipment (balances, pipettes, pH meter, UV-Vis, etc.) + Be proficient in Microsoft Excel and Word + Must have basic chemical knowledge and be able to handle materials safely. + Must be able to communicate effectively with manufacturing and quality personnel. + Must be able to effectively multitask.