Associate Director - MES Architect & Technical Lead

Role Summary

Associate Director – MES Architect & Technical Lead. This role is part of Tech@Lilly MQ (Manufacturing and Quality) and focuses on delivering Manufacturing Execution Systems (MES) using Syncade modules to enable world-class manufacturing performance. Responsible for both architectural and technical components of the MES solution, aligning with strategic objectives and operational requirements, and establishing standards and frameworks across sites.

Responsibilities

• Define and maintain direction for Syncade Solution Architecture in collaboration with the global Syncade Group, including standards, best practices, and technical frameworks.
• Provide expert guidance on design, implementation, and optimization of MES architecture to meet strategic and operational needs.
• Establish strategic roadmaps and site design evolution for API MES solutions and interfaces to MES.
• Define global IT support and delivery processes; monitor solution delivery for compliance with reference architecture.
• Lead or facilitate proof-of-concepts to clarify future state directions; test and certify innovative technologies as needed.
• Collaborate with Enterprise Architects, Data Management, Cybersecurity, and Protect Lilly teams to ensure alignment with standards and security requirements.
• Interface between IT and Business Partners on large projects (reporting, archival, performance, MES scope expansions).
• Mentor MES team members and drive value by implementing appropriate technical solutions; develop business cases related to MES.
• Identify trends and opportunities; maintain industry awareness and relationships to keep Lilly aligned with market practices.
• Find innovative ways to leverage Syncade to drive business value.

Qualifications

• Education: Bachelor‚Äôs degree in Computer Science, Engineering or related field
• Experience: Minimum 10 years of experience in MES
• Knowledge: Strong knowledge of distributed S95 Level 3 solutions, COTS software, and business intelligence; strong technical skills in infrastructure, interfaces, and configuration
• Skills: Strong analytical/problem-solving abilities; risk assessment and decision-making; excellent communication and leadership skills
• Experience in Pharma and GMP Manufacturing

Additional Preferences

• Experience managing programs/projects in the pharmaceutical business; startup experience for a new facility or clinical development manufacturing site
• Proven leadership in managing cross-functional teams
• Active participation in industry forums and standards organizations

Other Information

• Role is on-site, Monday through Friday; some extended or off-hour work may be required; travel 5-10%
• Roles based in Indianapolis IN, Houston TX, or Goochland, VA