Eurofins PSS is currently hiring for a QC Analytical Chemist to support GMP testing of pharmaceutical in-process, raw materials, intermediates, APIs, and stability samples. In addition, the successful candidate will support investigations of invalid results and method transfer activities. This individual will have high attention to detail and possess excellent organizational skills. Key Responsibilities: Conduct testing and review in accordance with approved methods, specifications, protocols, and compendial requirements Follow protocols for GMP regulations, including 21 CFR Parts 210 and 211, and applicable ICH guidelines Testing of pharmaceutical samples including in-process, raw materials, intermediates, API, stability, and more. Participate in method transfer, qualification, and verification studies Support investigations for OOS, OOT, and invalid results Utilize various analytical techniques including: NMR, GC, LC, ICP-OES, IR, RI, UV-Vis, Conductivity, Specific Rotation, Titration, TGA, and more Reference standard qualification and management Elemental impurities and residual solvent testing and review