PharmaSuite MES Consultant

Accenture is a business reinvention and technology company. Our ambition is to be the reinvention partner of choice for our clients and lead in the safe, widespread adoption of AI, and to be the most client-focused, AI-enabled, great place to work in the world. Our approximately 814,000 people bring deep insights across industries and functions, with capabilities spanning strategy, process, operating model, change management, talent, data, technology and AI. We deliver this expertise through consulting, managed services, proprietary assets and platforms, and increasingly, software. We bring innovation and new solutions informed by our experience across industries, enabling us to apply relevant insights, capabilities and leading practices from adjacent sectors to address emerging business challenges and opportunities. We serve more than 9,000 clients and generated revenues of approximately $74 billion in fiscal year 2026. Visit us at accenture.com. MES Consultant – Rockwell FactoryTalk PharmaSuite Join our SC&E – Life Sciences team as an MES Consultant and contribute to the design and implementation of Manufacturing Execution System solutions for pharmaceutical manufacturing environments. You will work with Rockwell FactoryTalk PharmaSuite to transform manufacturing and quality requirements into validated electronic workflows, supporting digitalization, automation and operational excellence in highly regulated GxP environments. The position is preferably based in Madrid or Barcelona, under a hybrid working model combining remote working days with time at the office, where you will have the opportunity to collaborate closely with your team and build strong working relationships. The work • Design, build, configure and test electronic batch records and manufacturing workflows in Rockwell FactoryTalk PharmaSuite, translating master batch records, production processes and quality requirements into validated MES solutions. • Configure and support MES processes covering order and recipe management, production reporting, inventory control, electronic records and quality assurance, ensuring alignment with pharmaceutical manufacturing processes and GxP requirements. • Execute Computer System Validation activities across the application lifecycle, supporting CSV/CSA documentation, testing, traceability and validation evidence required for regulated manufacturing systems. • Collaborate with Process, Automation, Quality Assurance and IT teams on MES integration and shop-floor architecture, including interfaces with technologies such as FactoryTalk Batch, KepwareEx and SAP/ERP systems. Responsibilities • Analyze business, manufacturing and quality requirements and translate them into detailed functional and technical MES specifications. • Configure and validate Rockwell FactoryTalk PharmaSuite solutions, including electronic batch records, recipes, manufacturing workflows, production reporting and associated master data. • Apply GxP and Computer System Validation principles throughout design, configuration, testing, deployment and application lifecycle activities, ensuring data integrity and traceability. • Contribute technical expertise to solution design decisions, issue resolution and continuous improvement initiatives, coordinating with Process, Automation, QA and IT stakeholders. Essential requirements • Minimum 3-4 years of professional experience working with Rockwell FactoryTalk PharmaSuite in MES implementation, configuration, design or support activities. • Minimum 3-4 years of professional experience working with Manufacturing Execution Systems (MES), including the design, configuration, implementation or validation of manufacturing workflows. • Minimum 3-4 years of professional experience in Life Sciences or pharmaceutical manufacturing environments. • Minimum 3-4 years of professional experience applying GxP requirements to regulated manufacturing systems and processes. • Minimum 3-4 years of professional experience performing Computer System Validation (CSV) activities for regulated systems. • Bachelor's or Master's degree in Engineering, including Industrial Engineering, Automation Engineering, Computer Engineering, Telecommunications Engineering or a comparable engineering discipline. • English level C1 or equivalent professional proficiency. • Residence in Spain and valid authorization to work in Spain. Nice-to-have requirements • Experience integrating or working with SAP/ERP solutions in manufacturing environments. • Experience with KepwareEx for industrial connectivity and shop-floor integration. • Experience with Rockwell FactoryTalk Batch in manufacturing or process automation environments. • Experience integrating MES applications with automation and enterprise platforms in Life Sciences manufacturing environments. • Experience designing or configuring electronic batch records and recipe-management processes. Generative AI Knowledge and experience in the use of generative artificial intelligence and AI tools applied to the role are required, in line with Accenture's commitment to the responsible and effective use of AI. Selection process To assess your fit with the position and Accenture's culture, you will participate in interviews with Talent Acquisition and the Hiring Manager, where we will explore your experience, motivations, competencies and expectations. If the process is successful for both parties, we will move to the offer stage, where we will present the terms of the position and compensation proposal. Our team will then support you throughout the onboarding process until you join Accenture. What does Accenture offer you ? At Accenture, you will enjoy a flexible, hybrid working model while being part of a company committed to inclusion, diversity and people's development. In addition, you will benefit from: • Medical, life and accident insurance. • Medical services and wellbeing programs. • Flexible compensation and employee share purchase program