2–5 years of experience in pharmaceutical QC/Stability studies; sound knowledge of GLP, GDP, stability protocols, environmental monitoring, and laboratory documentation.
Perform environmental monitoring of stability chambers; analyze stability, finished product, and raw material samples; manage stability sample receipt, issuance, reconciliation, and records; compile stability data and reports; prepare stability protocols and summaries; ensure alarm validation, GLP/GDP compliance, audit readiness, and proper laboratory maintenance.
