Manufacturing Execution Systems Specialist

Join us at Industry X, where we innovate, enhance intelligence, and promote sustainability in manufacturing. We empower leaders to effectively transition into the future, making manufacturing smarter, more connected, and sustainable. At Industry X, you'll be part of a team renowned for delivering swift results, helping clients thrive in a rapidly changing industrial landscape. As part of our Manufacturing & Operations practice, you will focus on transforming our clients' core manufacturing processes. Our specialists in Digital Production & Operations drive modernization with expertise in Execution Systems (MES/MOM), Automation, and Plant Data Models. You Are: A motivated Manufacturing Systems (MES) Specialist eager to embrace new opportunities. As industries advance towards digitalization, MES plays a vital role in achieving manufacturing excellence. Your Responsibilities: Lead the design, documentation, and implementation of Manufacturing Execution Systems (MES). Create and configure Electronic Batch Records (EBR). Implement MES solutions and seamlessly integrate with ERP and control equipment. Document MES configurations and validate EBR processes. Provide oversight for complex systems related to MES development. Collaborate with business management and users to define needs and design valuable solutions. Partner with clients to identify and implement the right solutions. Guide teams in execution of these tasks. Analyze business information needs to ensure timely and appropriate solution delivery. Gather user requirements for controlling and recording manufacturing activities. Respond to client proposal requests. Nurture client relationships effectively. Oversee global system implementations. Manage small to medium teams and projects. Travel Requirements: Travel may vary from 0 to 100% based on business needs and client requirements. Job Requirements: At least 1 year of experience with Rockwell FactoryTalk PharmaSuite (FTPS) in a highly automated Life Sciences manufacturing environment. Bachelor's Degree or equivalent experience (minimum 3 years). If you have an Associate's Degree, a minimum of 6 years of relevant experience is expected. Preferred Qualifications: Familiarity with FDA and GMP guidelines. Understanding of Life Sciences validation processes. Working knowledge of the Software Development Life Cycle (SDLC) and support methodologies. Strong communication skills, both written and oral. Ability to work collaboratively in a team-oriented environment. Competence in facilitating meetings and following up on action items. At Accenture, compensation varies based on various factors, including office location and role. The hourly salary ranges for different locations are provided based on local laws. We continuously accept applications and encourage you to apply! Accenture supports diversity and inclusion, ensuring equal employment opportunities and promoting a culture free of discrimination. We value the individuality of each team member and seek to create an environment that fosters innovation and creativity. If you need accommodation for the application process due to disability or religious observance, please reach out to us. We are committed to ensuring accessibility for all candidates.