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.
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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 Areas
MES 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 role
As 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 Skills
While you don't need all of them, experience across severa
📌 Supply chain (Barcelona)
🏢 Accenture
📍 Barcelona
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