Process Engineer (R2-R4)

Lilly • Indianapolis, IN

2d • $113,360 - $130,364 • Onsite

About The Position

Eli Lilly and Company seeks a Process Engineer (R2-R4) to support and continuously improve delivery devices, sub-assemblies, and components for packaging and manufacturing sites. Ensure compliance with current Good Manufacturing Practices (cGMPs), Health, Safety, and Environment (HSE) guidelines and regulations, company standards, and regulatory requirements. Develop, monitor, and provide technical oversight for control systems for process indicators to identify and address performance issues. Lead investigations concerning process and equipment safety incidents. Perform and summarize improvement opportunities in technical studies, reports, investigations, data analysis, and process modeling. Provide technical assessments of Original Equipment Manufacturer (OEM) technical proposals and make recommendations related to suitability. Support all aspects of tool and process qualification, including computer system validation.

Requirements

• Bachelor’s degree in Industrial Engineering, Mechanical Engineering, Chemical Engineering, or a closely related STEM field and 4 years of experience with process and equipment requirements in pharmaceutical manufacturing.
• Master’s degree in Industrial Engineering, Mechanical Engineering, Chemical Engineering, or a closely related STEM field and 3 years of experience with process and equipment requirements in pharmaceutical manufacturing.
• 3 years of experience with programming and debugging Programmable Logic Controllers (PLCs) and Human Machine Interfaces (HMIs).
• 3 years of experience with leading resolution of manufacturing-related issues, including deviations, data review, and supply chain coordination using Root Cause Analysis tools.
• 3 years of experience with computer-aided design tools.
• 3 years of experience with identifying and implementing process and product changes to improve manufacturing processes.
• 3 years of experience with using DOE, Six Sigma, and statistical methods as applied to engineering studies and reports.

Responsibilities

• Support and continuously improve delivery devices, sub-assemblies, and components for packaging and manufacturing sites.
• Ensure compliance with current Good Manufacturing Practices (cGMPs), Health, Safety, and Environment (HSE) guidelines and regulations, company standards, and regulatory requirements.
• Develop, monitor, and provide technical oversight for control systems for process indicators to identify and address performance issues.
• Lead investigations concerning process and equipment safety incidents.
• Perform and summarize improvement opportunities in technical studies, reports, investigations, data analysis, and process modeling.
• Provide technical assessments of Original Equipment Manufacturer (OEM) technical proposals and make recommendations related to suitability.
• Support all aspects of tool and process qualification, including computer system validation.

Benefits

• company bonus (depending, in part, on company and individual performance)
• company-sponsored 401(k)
• pension
• vacation benefits
• medical, dental, vision and prescription drug benefits
• flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
• life insurance and death benefits
• certain time off and leave of absence benefits
• well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level