Descripción de la oferta
A leading engineering group in Barcelona is looking for a Senior Validation Specialist with over 8 years of experience in pharmaceutical manufacturing specializing in oral solid dosage processes. This role involves executing validation activities in a GMP-regulated environment and collaborating with multiple teams. Ideal candidates must be bilingual in English and Spanish, possess strong technical writing skills, and have expertise in cGxP and regulatory compliance, making a meaningful impact in the healthcare technology sector.#J-18808-Ljbffr
