Quality Control Analyst II

Role: QC Analyst II supporting analytical chemistry testing within a regulated pharmaceutical environment. Responsibilities: perform analytical testing of raw materials, in-process, finished goods, and stability samples using chromatography, spectroscopy, and wet chemistry techniques; operate and maintain laboratory instrumentation (HPLC, GC, UV/Vis, FTIR, pH meters, etc.); ensure compliance with GMP, GDP, and regulatory standards; review data, support method development, transfer, validation, and troubleshooting; participate in investigations and continuous improvement initiatives. Requirements: Bachelor’s in Chemistry or related; 2–5 years’ experience in FDA-regulated pharma or medical devices; strong knowledge of GMP, ISO, and analytical techniques including HPLC and GC; proficiency with lab instruments and documentation practices. Preferred: experience with GC/MS, TOC analyzers, stability testing, method transfer, and trending activities; capable of supporting regulatory compliance and data integrity in a fast-paced environment. High-Value: analytical chemistry within pharma/medical device sectors, GMP compliance, regulated testing, method validation, equipment maintenance, cross-functional collaboration. WorkSetup: primarily on-site with flexibility; schedule support as needed.