QC Incoming Associate

Manage retain samples of Raw Materials, Finished Goods, and Bulk by storing them under specified temperature and humidity conditions to prevent integrity loss. Document reserve samples on logbooks and electronic systems to ensure traceability while conducting periodic visual inspections of Controlled Substances. Prepare reports regarding inventory and expiration of samples, identifying when retention periods are met or exceeded for disposal in accordance with regulatory standards. Document and report findings from visual evaluations of customer complaint samples to aid corrective actions, and contribute to investigations by gathering data and reviewing evidence. Requires a Bachelor's degree in a scientific discipline, at least three years of experience in pharmaceutical/biotech investigations, and bilingual Spanish and English proficiency.