Requires Master’s in Chemistry, Medicinal Chemistry, Pharmaceutical Chemistry, or closely-related scientific field & 2 yrs experience in a pharmaceutical, regulated life sciences, or quality assurance environment: conducting pharmaceutical quality testing of intermediates and final products in a GMP environment; reviewing analytical data & test results, including method validation reports, stability reports, and calibration and preventative maintenance reports; writing deviations & CAPAs; adhering to GMP requirements; and using ECM OpenLab, SAP, Trackwise, LIMS, Agilent, Empower and/or related software tools to document test results and data. Will also accept Bachelor’s in said fields & 5 yrs progressive, post-Bachelor’s stated experience.
