The role at Elanco focuses on supporting the operation, control, and optimization of manufacturing assets and technical processes at the Elwood, Kansas monoclonal antibody facility. The team is dedicated to ensuring compliance with cGMP standards while driving continuous improvement initiatives. As a subject matter expert, you will contribute to troubleshooting, data analysis, and technology transfer. This position offers the opportunity to work on both local and large-scale capital projects, enhancing the future of biologics manufacturing.

• Bachelor’s degree in Life Sciences, Electrical Engineering, Industrial Engineering, Mechanical Engineering, or a related field.
• 3 years of progressively responsible post-baccalaureate experience in the job offered or any engineering-related roles.
• Experience in pharmaceutical, biotechnology, or a related industry.
• Knowledge of cGMP standards and experience working in a regulated environment.
• Familiarity with aseptic processing techniques and cleaning/sanitization methodologies.
• Experience with Process Validation, risk assessments (FMEA), and Process Performance Qualifications (PPQ).
• Ability to interpret and comply with USDA/FDA/EMA regulations.
• Proficiency in utilizing statistical tools to analyze process trends and determine corrective actions (CAPA).
• Experience operating and maintaining Single-Use Bioreactor Systems, SCADA, and MES.

• Support the operation, control, and optimization of manufacturing assets and technical processes.
• Serve as a subject matter expert in process and equipment performance.
• Contribute to development, data analysis, troubleshooting, technology transfer, and continuous improvement initiatives.
• Support local and large-scale capital projects, including equipment design, installation, commissioning, qualification, and validation.
• Provide technical expertise and engineering solutions for process and equipment-related challenges.
• Troubleshoot issues on the manufacturing floor to ensure reliable performance.
• Ensure processes and equipment operate in a controlled, compliant state aligned with cGMP standards.
• Support investigations, root cause analysis, and implementation of CAPA.
• Utilize data-driven insights to monitor performance and implement improvements.
• Support the full lifecycle of capital projects, including design, installation, commissioning, qualification, and validation.
• Ensure all changes to processes and equipment are properly assessed and documented.
• Maintain and review technical documentation such as process flows, specifications, and validation protocols.
• Collaborate with Manufacturing, Quality, Engineering, and other teams to resolve technical challenges.

• Employees at Elanco are often offered competitive compensation with annual bonus and equity eligibility, retirement plans (including a U.S. 401(k)), and comprehensive health coverage—medical, dental, vision, company-paid life and disability—and even pet insurance. Time-off and flexibility typically include generous PTO, U.S. mid-year and year-end paid shutdown weeks, parental leave, and flexible/remote work options. Employees also benefit from strong development programs (onboarding, course libraries, mentorship, nine ERGs, and tiered leadership programs) that support both professional growth and community involvement.