Syner-G BioPharma Group in the United States seeks a Senior Validation Engineer (QAV) with 4‐15 years of experience to support validation across equipment, utilities, facilities, computerized systems, manufacturing processes, and MES/eBR in GMP environments. You will develop, execute, review, and maintain validation lifecycle documentation, ensuring regulatory compliance, data integrity, and alignment with GMP requirements while collaborating with cross-functional teams for system releases and
