Scientist, Analytical Chemistry

Role: Mid-level Scientist in Analytical Chemistry supporting pharmaceutical oral dosage form development, focusing on analytical method development, validation, transfer, and routine testing within a QC environment. Responsibilities: perform physical and chemical analyses of raw materials, in-process, and finished products, including stability samples; develop and validate analytical methods (mainly LC and GC); calibrate laboratory instrumentation; document and review testing results; provide technical guidance and training to analysts; participate in investigations of out-of-specification results; recommend new analytical technologies; contribute to laboratory efficiency and GMP compliance. Requirements: Bachelor's in chemistry or related field; 3+ years pharmaceutical experience (1+ with Master's); extensive hands-on experience with HPLC, GC, dissolution testing, spectrophotometry, FTIR, TLC, and MS; strong knowledge of cGMP standards, compendial procedures (USP/EP/BP/JP), and analytical method validation. Preferred: MS/MA in chemistry or pharmaceutical sciences. HighValue: expertise in analytical chemistry for pharmaceuticals, quality control testing, method development and validation, GMP compliance, stability studies, and regulatory documentation. WorkSetup: not specified; likely on-site based on laboratory nature.