Quality Control Analytical Chemist II – Malvern, PAResponsibilities:Calibrate, maintain and operator laboratory equipment such as HPLC, GC, GC-HS, FTIR, pH meter, balances, KF, titrators and LCMSConduct GMP analyses of raw materials, in-process materials, final product, and stability samplesComplete GMP documentation needed to support release of raw materials, intermediates, and final productsValidate methods for use in GMP environmentPrepare documents such as methods of analysis, specifications, analytical reports etc.Provide analytical support to Process R&D (synthetic R&D) group and collaborate to advance the projectParticipate in method development and optimization as necessaryQualifications:Typically, BS w/ 3-5 years relevant experience or MS w/+2-year relevant experience in pharmaceutical industry. (or relevant fields)Previous QC/method development experience well consideredKnowledge of cGMP regulations, USP, and chromatographic software is required.Excellent organizational, communication and documentation skills required.Prepositive approach and interest in analytical development, well considered.No fields configured