Bilingual EU GMP Auditor - ATMP Onsite in Spain

The FDA Group seeks a bilingual Spanish/English GMP Audit Consultant to support a focused two-day onsite audit at a life sciences site in Spain. The consultant will prepare, execute, and document findings, evaluating EU GMP compliance for ATMP manufacturing and inspecting records and documentation in Spanish. Fluency in Spanish and English is essential; travel to the facility in Southern Spain is required, with onsite work and remote preparation support.