Associate Director-Engineering
Eli Lilly and Company
2 hours ago
Remote friendly (Indianapolis, IN)
United States
$117,000 - $171,600 USD yearly
Operations
Position Brand Description:
Accomplished maintenance engineering professional with expertise in CMMS, specializing in Maximo platform operations, data analytics, and maintenance process optimization within pharmaceutical operations. Deliver technical solutions, ensure regulatory compliance, and drive business process improvements through innovative technology.
Key Objectives/Deliverables:
- Lead consolidation of multiple Maximo instances into a global platform; support maintenance processes including asset management, work orders, preventative maintenance, and calibration.
- Develop dashboards, reports, and analytics using Tableau, Power BI, and SQL to drive operational insights and performance.
- Implement integration processes for condition-based maintenance; optimize CMMS functionality to reduce downtime.
- Ensure data integrity (ALCOA+) and compliance with GMP/GLP standards.
- Provide technical consulting, troubleshooting, and root cause analysis for global maintenance teams.
- Support knowledge sharing, training, and continuous improvement initiatives, including Lean programs.
- Collaborate with IT and engineering teams on system upgrades, enhancements, and best practices.
- Contribute to global standards, guidance documents, and process improvement projects.
Minimum Requirements:
- Bachelor’s degree and 10 years’ relevant experience OR 12+ years of relevant experience.
- Experience with Maximo/CMMS consolidation and large-scale implementations.
- Experience in pharmaceutical or GMP/cGMP manufacturing environments.
- Experience supporting multi-site operations, preferably global.
Preferences:
- Business intelligence/analytics (Tableau, Power BI, SQL).
- Condition-based maintenance and equipment reliability program knowledge.
- Experience with Maximo (GMARS), Asset & Work Order Management, Preventative Maintenance, Equipment Reliability, Calibration, Planning & Scheduling, GMP/GLP compliance, and process optimization.
Additional Information (Role Expectations):
- Travel required (domestic and international) as needed (~10%).
- Fluent in English; additional languages recommended.
- Role may be based at US Eastern Time Zone manufacturing sites or at a Lilly EU/US manufacturing site.
Benefits (if eligible, per description):
- Company bonus; 401(k) with company sponsorship; pension; vacation; medical/dental/vision/prescription benefits; flexible benefits; life insurance/death benefits; time off/leave; well-being benefits (EAP, fitness, clubs/activities).
Application Instructions:
- If you require accommodation to submit a resume, complete the accommodation request form: https://careers.lilly.com/us/en/workplace-accommodation.
Accomplished maintenance engineering professional with expertise in CMMS, specializing in Maximo platform operations, data analytics, and maintenance process optimization within pharmaceutical operations. Deliver technical solutions, ensure regulatory compliance, and drive business process improvements through innovative technology.
Key Objectives/Deliverables:
- Lead consolidation of multiple Maximo instances into a global platform; support maintenance processes including asset management, work orders, preventative maintenance, and calibration.
- Develop dashboards, reports, and analytics using Tableau, Power BI, and SQL to drive operational insights and performance.
- Implement integration processes for condition-based maintenance; optimize CMMS functionality to reduce downtime.
- Ensure data integrity (ALCOA+) and compliance with GMP/GLP standards.
- Provide technical consulting, troubleshooting, and root cause analysis for global maintenance teams.
- Support knowledge sharing, training, and continuous improvement initiatives, including Lean programs.
- Collaborate with IT and engineering teams on system upgrades, enhancements, and best practices.
- Contribute to global standards, guidance documents, and process improvement projects.
Minimum Requirements:
- Bachelor’s degree and 10 years’ relevant experience OR 12+ years of relevant experience.
- Experience with Maximo/CMMS consolidation and large-scale implementations.
- Experience in pharmaceutical or GMP/cGMP manufacturing environments.
- Experience supporting multi-site operations, preferably global.
Preferences:
- Business intelligence/analytics (Tableau, Power BI, SQL).
- Condition-based maintenance and equipment reliability program knowledge.
- Experience with Maximo (GMARS), Asset & Work Order Management, Preventative Maintenance, Equipment Reliability, Calibration, Planning & Scheduling, GMP/GLP compliance, and process optimization.
Additional Information (Role Expectations):
- Travel required (domestic and international) as needed (~10%).
- Fluent in English; additional languages recommended.
- Role may be based at US Eastern Time Zone manufacturing sites or at a Lilly EU/US manufacturing site.
Benefits (if eligible, per description):
- Company bonus; 401(k) with company sponsorship; pension; vacation; medical/dental/vision/prescription benefits; flexible benefits; life insurance/death benefits; time off/leave; well-being benefits (EAP, fitness, clubs/activities).
Application Instructions:
- If you require accommodation to submit a resume, complete the accommodation request form: https://careers.lilly.com/us/en/workplace-accommodation.