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Sr Director - Tech at Lilly Manufacturing & Quality

Eli Lilly and Company
Full-time
On-site
Houston, TX
$157,500 - $231,000 USD yearly
IT

Role Summary

Sr Director - Tech at Lilly Manufacturing & Quality leads IT strategy and operations for new API manufacturing site initiatives, reporting to senior IT and site leadership. Responsible for shaping the Digital agenda, coordinating start-up and integration of IT systems, and building a high-performance team to support manufacturing facilities.

Responsibilities

  • Ensure site operational readiness from IT perspective and lead site start-up and IT system integration including infrastructure, warehouse management & logistics, data historian, real-time floor tracking, digital plant, laboratory information management, CAPA systems, access security, building monitoring, risk management, and MES.
  • Serve as a member of the Site Leadership Team and provide IT site functional leadership.
  • Develop and implement site IT strategic and business plans; benchmark innovative solutions; adapt roadmaps to site evolution and trends; partner cross-functionally to implement site IT roadmap; maintain a safe work environment.
  • Ensure staffing to meet site and functional agenda; lead, coach, and develop team members; foster Lilly-values-based culture and operational excellence; lead recognition, pay, and promotion decisions; lead talent assessment and succession planning; support site recruiting to build IT capability.
  • Maintain a functionally strong, operationally centered IT organization; ensure a solution-focused organization; prioritize and remove barriers; oversee technical activities and promote knowledge sharing and education.

Qualifications

  • Required: Bachelorโ€™s Degree in IT, Computer Science, Engineering, or related technical field; 10+ years of leadership in Pharma IT with manufacturing IT/OT leadership experience.
  • Preferred: 10+ years of experience with MES system implementations, data integration, and advanced analytics.

Skills

  • Deep knowledge of regulatory compliance (cGMP)
  • Proven leadership and team-building excellence
  • Agile management of multiple projects with adaptability to shifting priorities
  • Collaborative cross-functional teamwork
  • Exceptional written and verbal communication
  • Creative and analytical mindset for complex issue resolution
  • Deep technical knowledge of pharmaceutical manufacturing and IT/OT footprints
  • Problem-solving and troubleshooting capabilities

Education

  • Bachelorโ€™s Degree in IT, Computer Science, Engineering, or related field

Additional Requirements

  • Location: Houston, TX or Richmond, VA with travel up to 50% to other US and global Lilly sites
  • Role is on-site, Monday through Friday; occasional extended or off-hours work may be required
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