Associate Director - MES Architect & Technical Lead

Role Summary

Associate Director – MES Architect & Technical Lead. This role focuses on delivering Manufacturing Execution Systems (MES) using Syncade modules, guiding architectural and technical direction, and collaborating across global teams to ensure scalable, reliable MES solutions in Lilly’s new API manufacturing environments.

Responsibilities

• Lead architectural and technical components of the MES solution, aligning with strategic objectives and operational requirements.
• Establish and maintain direction for Syncade Solution Architecture in collaboration with the global Syncade Group; define standards, best practices, and technical frameworks.
• Anticipate MES needs from an IT Architecture standpoint and shape a strategic roadmap for API MES solutions.
• Collaborate with global Architects, Enterprise Architects, local IT teams, data management, cybersecurity, and business partners to design, implement, and optimize MES systems.
• Provide deep technical knowledge, monitor delivery projects for compliance with reference architecture, and facilitate proof-of-concepts for future state direction.
• Lead or support business case development related to MES; influence business to drive value and implement appropriate technical solutions.
• Coach/mentor MES team members and others on technologies, architecture, and technical design.
• Identify new trends/opportunities; maintain relationships with industry peers to stay competitive.
• Drive innovative use of Syncade to deliver business value.

Qualifications

• Education: Bachelor’s degree in Computer Science, Engineering or related field
• Experience: Minimum 10 years of experience in MES
• Knowledge: Distributed S95 Level 3 solutions, commercial configurable software (COTS), business intelligence; strong technical skills including infrastructure, interfaces and configuration
• Skills: Strong analytical and problem-solving abilities; excellent communication and leadership to interact with stakeholders at all levels
• Experience in Pharma and GMP Manufacturing

Additional Preferences

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

Other Information

• On-site role, Monday through Friday; occasional extended hours or off-hours support may be required
• Multiple positions based in Indianapolis, IN; Houston, TX; or Goochland, VA
• Travel: 5-10% of time