The role at Elanco focuses on supporting the operation, control, and optimization of manufacturing assets and technical processes at the monoclonal antibody manufacturing facility in Elwood, Kansas. The position requires acting as a subject matter expert in process and equipment, engaging in development, data analysis, troubleshooting, and continuous improvement activities. The successful candidate will provide technical support and engineering solutions for process-related issues while ensuring compliance with regulatory commitments and quality standards. This role emphasizes collaboration and innovation within a diverse and inclusive work environment.

• Master's degree in Engineering Management, Mechanical Engineering, or a related field, or a foreign equivalent plus 1 year of post-baccalaureate experience in the job offered or any research scientist related job titles.
• 1 year of experience in the medical device, pharma, or biotechnology industry.
• Experience with Installation Qualification (IQ), Operational Qualification (OQ), Validation, and Installation.
• Familiarity with cGMP standards and experience working in a regulated environment.
• Knowledge of GMP documentation, Safety, Standard Operating Procedures (SOP), Batch Documents, Change Control, Protocol Execution, and Deviation investigation.
• Experience with Statistical Process Control (SPC) to monitor and control process parameters.
• Experience in the development and analysis of design scope for manufacturing equipment.
• Experience providing maintenance guidance for manufacturing equipment.

• Support the operation, control, and optimization of manufacturing assets and technical processes.
• Act as a subject matter expert for process and equipment.
• Engage in development, data analysis, troubleshooting, and continuous improvement activities.
• Provide technical support and engineering solutions for process and equipment-related issues.
• Ensure compliance with regulatory commitments, GMPs, and Elanco standards.
• Document changes appropriately through the change management system.
• Participate in design, development, execution, commissioning, qualification, and validation activities for major projects.
• Collaborate with team members to identify potential risks and improvement opportunities.
• Create, review, and revise relevant documentation including user requirement specifications and commissioning documents.
• Manage Quality events such as Deviation, Change Control, and CAPA.

• 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.