Our Manufacturing Execution Systems (MES) practice designs, builds, and validates the platforms that run regulated pharmaceutical manufacturing — connecting the shop floor to the enterprise while meeting the highest standards of quality and data integrity.¿Interesado en saber más sobre este trabajo? Desplácese hacia abajo y descubra qué habilidades, experiencia y cualificaciones académicas se necesitan.As our MES for Life Sciences work continues to grow, we are looking for detail-driven professionals to join our validation team and help bring compliant manufacturing systems to life.Our Focus AreasMES Implementation – End-to-end rollout of FactoryTalk PharmaSuite and the Rockwell automation stack across pharmaceutical sites.Computer System Validation – Risk-based CSV and CSA delivery that keeps GxP systems compliant and audit-ready.Data Integrity – Embedding ALCOA+ principles and 21 CFR Part 11 / EU GMP Annex 11 controls into every system we deliver.Systems Integration – Connecting MES to ERP, historians, and process control via industry standards.Your roleAs an MES Validation in Accenture Industry X, you will:Author and execute IQ, OQ, and PQ protocols for FactoryTalk PharmaSuite configurations.Maintain traceability between user, functional,



and design requirements and test evidence.Apply GAMP 5 and risk-based validation approaches to define and document validation scope.Collaborate with configuration and quality teams to investigate, remediate, and document deviations.Support data integrity controls aligned to ALCOA+ across the system lifecycle.What Skills Are We Looking For?Basic Qualifications Bachelor's or Master's degree in Life Sciences, Engineering, Computer Science, or a related field. Proficiency in English (Spanish is a plus). Previous experience in computer system validation, quality, or MES delivery in a regulated environment (hiring at multiple levels).Technical SkillsWhile you don't need all of them, experience across several areas will be highly valued:Validation & Compliance: CSV/CSA or ALCOA+ data integrity.MES Platforms: Rockwell FactoryTalk PharmaSuite (or comparable regulated MES such as PAS-X, Opcenter).Testing & Lifecycle: IQ/OQ/PQ authoring and execution, requirements traceability, deviation management.Tools: SQL querying, Application Lifecycle Management / test management tooling.Life Sciences Manufacturing: understanding of GxP/GMP production processes.Soft & Strategic SkillsAttention to Detail: Maintain documentation rigor and evidence quality under audit scrutiny.Problem-Solving: Investigate deviations and propose practical, compliant remediations.Communication & Collaboration: Work effectively with configuration, quality, and client teams. xcskxlj Agility: Adapt across fast-moving project phases from configuration through hypercare.

📌 Supply chain & Engineering_MES Validation Analyst (Barcelona)
🏢 Accenture
📍 Barcelona