Greenville, NC30+ days ago
Executes validated test methods for pharmaceutical in-process samples, finished product samples, stability samples and cleaning samples for strength, impurities and identity by HPLC, GC and spectroscopy, and traditional quantitative analysis, utilizing HPLC, GC, spectroscopy, and/or traditional wet chemical testing. With global operations, we support active pharmaceutical ingredients (APIs), biologics, cell and gene therapy, viral vectors, formulation, clinical trials, logistics, commercial manufacturing, and packaging, delivering integrated solutions that help bring life-changing medicines to patients faster.