QA Specialist I: GMP Batch Review & Compliance

A leading services supplier in the pharmaceutical industry is looking for a QA Specialist I. This role involves reviewing batch records to ensure compliance with quality standards and regulations. Candidates should have a Bachelor's Degree in Science and a minimum of 2 years of experience in biotechnology manufacturing. Knowledge of SAP, LIMS, and MES is required. The position offers a temporary employment type with a Monday to Friday schedule from 8-5. Bilingual communication skills in English and Spanish are essential. #J-18808-Ljbffr