Senior Director, Engineering & Maintenance
Role Overview
The Site Sr. Director of Maintenance and Engineering provides strategic leadership and operational oversight for all engineering, maintenance, and utility functions at the Elwood manufacturing site. This role is a member of the Site Leadership Team and ensures that all physical assets and technical processes meet the highest safety and quality standards to support Elanco's mission.
Responsibilities
Strategic Asset Management: Develop and execute a multi-year engineering strategy aligned with Elanco 2030, utilizing Reliability Excellence (REx) to maximize asset uptime and support future site growth.
Capital Portfolio Leadership: Direct the site’s CAPEX investments and Master Plan, partnering with Global Engineering to deliver complex projects on time, within budget, and in full compliance.
Operational Excellence & Sustainability: Oversee reliable maintenance and utility operations using SAP-driven predictive programs while advancing energy efficiency in line with Elanco’s ESG goals.
Safety & Regulatory Compliance: Champion a "Safety First" culture, ensuring all technical processes and equipment meet rigorous GxP, HSE, and global regulatory requirements (FDA, USDA, etc.).
People & Financial Leadership: Lead and mentor a high-performing technical team while managing OPEX and CAPEX budgets to ensure fiscal responsibility and a values-driven work environment.
Qualifications
Education: Bachelor’s degree in an Engineering-related discipline.
Required Experience: 10+ years of experience in maintenance and/or engineering in a regulated industry, including 5+ years of leadership experience.
Proven track record of managing large-scale capital projects (>$10M).
Deep expertise in Reliability Excellence (REx) and Total Productive Maintenance (TPM).
Preferred Qualifications
Advanced degree such as MBA or MS in Engineering Management.
Experience in monoclonal antibody, vaccine and/or recombinant protein manufacturing.
Experience in biological manufacturing including cell culture, purification (separation technologies, chromatography, tangential flow filtration), viral inactivation and cleaning / sterilization processes in a biological environment.
Experience with SAP PM/MM modules.
Experience in commissioning, qualification and validation activities associated with aseptic processes, technology transfers and new product commercialization.
Experience in capital project design, development, and execution.
Understanding of USDA, FDA, and EU GMP regulatory standards for veterinary biologics.