Overview At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our more than 45,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. MES Solution Architect Position Title: MES Solution Architect Position Type: Full-time Job Family: Information Technology Location/s: Indianapolis, Charlotte, Raleigh-Durham, Kenosha, Puerto Rico, Alcobendas, Fegersheim, Alzey, Sesto Job Function: Tech@Lilly Tech Ladder (Y/N): Y Note: When applying internally for a position your current supervisor receives notification that you have applied to the position. We encourage employees to discuss the opportunity with their supervisor prior to applying. Lilly’s Purpose At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our more than 45,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Lilly is entering an exciting period of growth and we are committed to delivering innovative medicines to patients around the world. Lilly is investing around the world to create new state-of-the-art manufacturing site’s and continue expanding our existing facilities to created capacity required to continue with our mission. The brand-new facilities will utilize the latest technology, advanced highly integrated and automated manufacturing systems, and have a focus on minimizing the impact to our environment. Position Brand Description We are on an ambitious journey to transform our manufacturing operations, and the Manufacturing Execution System (MES) is pivotal to achieving this transformation. Multiple projects are currently underway to expand the footprint of MES, enabling new facilities to operate paperless and modernizing MES in established operations worldwide. Key Objectives/Deliverables Act as the process-specific design lead for Electronic Manufacturing Batch Records (MBRs), ensuring alignment with both global standards and site-specific requirements. Lead the design and configuration of MBRs for a given manufacturing or packaging process, collaborating closely with site teams and global Subject Matter Experts (SMEs). Identify synergies across manufacturing sites to drive harmonization and promote reuse of MBR components. Define and maintain clear boundaries between Global MBR content and Site-specific localization to ensure standardization and flexibility. Ensure that MBR designs reflect compliant, efficient, and scalable manufacturing processes. Collaborate with cross-functional teams (Technical Service /Manufacturing Science, Process Engineering, QA, IT) to gather process requirements and translate them into MES functional design. Serve as the main point of contact for MBR-related topics during NG MES deployments, from initial scoping to validation. Contribute to the creation and governance of Global Design Templates and Configuration Standards for MES. Provide guidance and coaching to local teams during MBR design and testing activities. Continuously improve the design process by incorporating lessons learned and best practices from prior deployments. Basic Requirements Education: Bachelor’s Degree in IT, Computer Science, Engineering, or equivalent years of experience. Minimum 7 years as an IT Business Integrator or IT Project Leader in Life Science Manufacturing. Understanding of GMP regulations and Computer System Validation (CSV) principles (e.g., GAMP 5, 21 CFR Part 11, Annex 11). Familiarity with MES platforms such as PharmaSuite (preferred), PMX, Werum PAS-X, Emerson Syncade, DeltaV or similar is strongly preferred. Ability to work cross-functionally and communicate effectively with technical and non-technical stakeholders. Proficiency in English (written and spoken). Additional Skills/Preferences Experience working globally, influencing without authority, and resolving complex issues. Learning agility, subject matter expertise in Life Sciences. Knowledge of Business Process development, SOPs, Governance Processes, and Program Management. Risk-based decision making, diverse communication methods, and strong account management skills. Additional Information Position locations: Indianapolis, Charlotte, Raleigh-Durham, Kenosha, Puerto Rico, Alcobendas, Fegersheim, Alzey, Sesto Occasional off-hours and weekend work expected. 10-15% domestic/international travel required. Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. WeAreLilly Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lillydoes not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. WeAreLilly J-18808-Ljbffr