Principal - Engineer - Automation (Data & Platforms integration)

Responsibilities Support the design and delivery of site data historian systems, key integration platforms, and system administration of site servers. Design and deliver data historian and integration platforms, including validation plans, system integrator selection/oversight, and site administrative procedures to maintain validated state. Support related automation platforms (including process automation servers and DeltaV DCS). Collaborate with Lilly Quality, engineering peers, A&E firms, and system integrators during delivery. After project delivery, support GMP manufacturing operations by providing data historian/integration services, system administration, and platform upgrades. Key Deliverables Champion a strong safety culture; mentor and coach others; apply engineering/automation fundamentals to design and problem solving. Become a subject matter expert on Lilly’s Aveva PI Data Historian reference architecture. Lead system integrations and OEM activities for design/installation of Aveva PI platforms, data centers, and related site infrastructure. Collaborate to develop computer system qualification and testing strategies. Ensure CSV documentation complies with corporate standards/templates and electronic document management system properties. Participate in basic/detailed design including staffing, statements of work, supplier management, and computer system validation delivery strategies. Develop and build capabilities within the Houston site automation team. Support development of site procedures for computer system validation and administration. Provide technical oversight for equipment/process system User Requirements and related Design Review/Qualification documentation. Basic Qualifications Bachelor’s degree in engineering or related discipline. 3+ years of Aveva PI Data Historian administration (hardware design, software integration, system procedures). Experience with Windows Servers and virtual environments. Additional Skills/Preferences 3+ years of pharmaceutical manufacturing experience preferred (other manufacturing considered). Strong analytical, writing, and critical thinking skills. Experience with Kneat Validation software, Veeva Vault, or similar. Ability to collaborate with others. Travel Potential for travel ( Benefits Eligibility for company-sponsored 401(k) Pension Vacation benefits Medical, dental, vision, prescription drug benefits Flexible benefits Life insurance / death benefits Time off / leave of absence benefits Well-being benefits (e.g., employee assistance program, fitness benefits, employee clubs / activities) #J-18808-Ljbffr