
Associate Director, Plant Engineering – Lilly Medicine Foundry
- Indianapolis, IN
- $118,500-173,800 per year
- Permanent
- Full-time
- Responsible for oversight of campus specific building area engineering personnel in regards to engineering lifecycle management of critical and non-critical activities associated with GMP clinical manufacturing and all necessary support functions.
- Ensure compliance related engineering and facilities activities such as deviations, change controls and CAPA’s (Corrective and Preventive Actions) are resolved and implemented in conjunction with Operations, Process Engineering, Supply Chain and Quality Assurance.
- Collaborate with Medicine Foundry key stakeholders along with global engineering and ETC (Engineering Technical Center) resources in order to drive and manage engineering related CAPEX projects for each building of the Lilly Medicine Foundry campus.
- Responsible for establishing and maintaining a GMP compliant site calibration program for all critical and non-critical instrumentation for the Medicine Foundry in alignment with Lilly global standards and procedures.
- Responsible for oversight and administration of the FUME organization’s CMMS (Computerized Maintenance Management System) for the Lilly Medicine Foundry in alignment with global engineering standards and practices.
- Implementing and overseeing a comprehensive planning / scheduling FUME (Facilities, Utilities, Maintenance and Engineering) function for the daily and future coordination of work activities including corrective / preventive maintenance, calibration, work readiness (kitting), engineering project support, planned shutdowns and critical spare parts management.
- Collaborate with both internal FUME resources and key stakeholders (Supply Chain, Operations and Quality) in order to align and bundle work packages to minimize facility / equipment downtime and customer interruption while driving overall plant throughput.
- Responsible for supervising, coaching and developing engineering personnel and other staff including completing performance evaluations and development planning.
- Identify, track and report key indicators of functional performance such as on time delivery, budget adherence and compliance related metrics.
- Ensure alignment and compliance with corporate engineering expectations (CMMS administration, calibration execution, scheduling performance, spare parts management etc). Actively work within the global engineering and ETC network to ensure alignment with corporate initiatives and utilization of best practices.
- Support site governance through participation, influence and leadership in cross functional meetings and initiatives.
- Build and lead a passionate high performing agile team that can adapt and thrive in a fluctuating and varying landscape in order to support the needs of the business.
- Build the organization with the necessary capability, capacity and culture to operate this facility to the highest standards of operational excellence.
- Develop and implement the systems and processes needed to run the site, leveraging existing Lilly knowledge and practices where necessary, but also incorporating external experiences and learning.
- Ensure regulatory compliance and operational excellence by supporting lean principles in their respective area.
- Support the global project team as they deliver the facility to the site team, by providing feedback and hands on support.
- Bachelor’s degree in Engineering or related field
- Minimum of 5 years of work experience in manufacturing / operations and/or engineering and previous supervisory experience in a GMP environment.
- Ability to work with a team, make independent decisions, and influence diverse groups.
- Ability to operate within a regulated industry and make risk-based compliance related decisions.
- Ability to instill teamwork within the department and demonstrate key interpersonal skills.
- Direct oversight in building and/or maintaining a GMP calibration program.
- Cross functional understanding of scheduling / planning impact of work packages in conjunction with manufacturing / operations.
- Engineering support experience in regards to quality management functions such as deviations, change control and CAPAs.
- Experience in oversight or working within a CMMS such as Maximo, Blue Mountain Regulatory Asset Manager, SAP Plant Maintenance, etc.
- Oversight of engineering related functions such as CAPEX management, building operations and change management.
- Ability to provide innovative solutions to plant, divisional, and corporate issues and leverage ideas from other functional areas.
- Be a passionate role model for team members in terms of performance and behaviors. Help people improve their performance and close performance gaps with appropriate training, professional development and coaching interventions.
- Initial location at Lilly Technology Center, Indianapolis.
- Permanent location at the new Lilly Medicines Foundry in Lebanon, Indiana.