Analyst III, QC Raw Materials

Role: Quality Control Raw Material Specialist focused on inspection, testing, and evaluation of raw materials within a biopharmaceutical manufacturing environment. Objectives include ensuring compliance with GxP, improving QC processes, and supporting raw material qualification and specifications. Responsibilities encompass performing analytical testing (spectroscopy, chromatography, wet chemistry), developing and revising test methods, managing laboratory documentation, coordinating with suppliers, and leading investigations for out-of-specification results and deviations. Qualifications: Bachelor's in Chemistry or related field with ≥5 years (or Master's with ≥3 years) of QC raw material experience; proficiency with analytical techniques, compendial methods, and regulatory standards; strong technical writing and data analysis skills; familiarity with GMPs and GLPs. Preferred: Experience in pharmaceutical QC testing, instrument qualification, and assay development. High-Value: Focus on raw materials testing, spectroscopic and chromatographic techniques, cGMP compliance, and experience in a pharmaceutical or biotech manufacturing setting. Collaboration involves internal QC, manufacturing, and external suppliers. Work Environment: On-site at EMOB facility; physical and safety considerations apply.