Senior Bioprocess Engineer — Transfer & Optimization

Eli Lilly and Company; Indianapolis (IN); On-site; USD 66,000 - 172,000; Full time

Benefits offered by this job

Company sponsored 401(k)

Pension

Vacation benefits

Medical, dental, vision benefits

Job summary

Eli Lilly and Company in Indianapolis, IN seeks an engineer for the Process Engineering group to support the manufacture of bulk drug substance (API) for development and clinical trials. The role bridges development and operations during technology transfer and serves as the primary contact for equipment troubleshooting.

You will monitor equipment performance, drive continuous improvement, and ensure qualification and compliance. A BS in engineering and 3+ years GMP experience are required.

Qualifications

• Bachelor of science in engineering (Chemical/Biomedical/Mechanical preferred).
• 3+ years in a manufacturing environment supporting GMP operations.
• Authorized to work in the United States without sponsorship.

Responsibilities

• Monitor equipment and process performance to identify risks and optimization opportunities.
• Provide input for technical transfer of new processes from development to manufacturing.
• Lead continuous improvement initiatives related to equipment performance and process capability.
• Ensure equipment remains qualified through maintenance and documentation.
• Develop and deliver training materials for equipment knowledge transfer.

Skills

Change Management

Root Cause Analysis

GMP operations

Industrial automation

Education

Bachelor of Science in Engineering

Tools

UNICORN

DeltaV

OSI PI

Job description

Eli Lilly and Company in Indianapolis, IN seeks an engineer for the Process Engineering group to support the manufacture of bulk drug substance (API) for development and clinical trials. The role bridges development and operations during technology transfer and serves as the primary contact for equipment troubleshooting.

You will monitor equipment performance, drive continuous improvement, and ensure qualification and compliance. A BS in engineering and 3+ years GMP experience are required.