Senior Bioprocess Engineer - Tech Transfer

BioSpace; Indianapolis (IN); On-site; USD 66,000 - 172,000; Full time

Benefits offered by this job

401(k) plan

Pension

Vacation benefits

Job summary

Lilly in Indianapolis is seeking a Process Engineer in the Bioprocess Clinical Trials Manufacturing Facility. You will support API production, interface between development and operations, and lead equipment qualification activities.

Responsibilities include monitoring equipment, driving CIP and continuous improvement, and ensuring compliance with HSE and Quality requirements. Strong GMP experience and a BS in engineering are required.

Qualifications

• Bachelor's degree in engineering (Chemical, Biomedical, or Mechanical preferred).
• 3+ years of experience in a manufacturing environment supporting GMP operations.
• Authorized to work in the United States on a full-time basis.

Responsibilities

• Monitor equipment and process performance to identify risks and optimization opportunities.
• Provide engineering input for technology transfer from development to manufacturing.
• Lead continuous improvement initiatives related to equipment performance and process capability.
• Maintain knowledge of manufacturing processes, equipment, facilities, and computer systems.
• Lead multi-disciplinary projects to scope, design, and implement goals.
• Serve as the primary resource for safety issues and CAPA related to supported processes.

Skills

Change management

Deviation management

Root cause analysis

Pharmaceutical experience

Safety and regulatory compliance

Education

Bachelor's degree in engineering (Chemical/Biomedical/Mechanical)

Tools

UNICORN

DeltaV

OSI PI

Job description

Lilly in Indianapolis is seeking a Process Engineer in the Bioprocess Clinical Trials Manufacturing Facility. You will support API production, interface between development and operations, and lead equipment qualification activities.

Responsibilities include monitoring equipment, driving CIP and continuous improvement, and ensuring compliance with HSE and Quality requirements. Strong GMP experience and a BS in engineering are required.