Cleanroom GMP Operator – Advanced Therapies

BioSpace; Lebanon (IN); On-site; USD 24,000 - 47,000; Full time

Benefits offered by this job

401(k) plan

Pension plan

Vacation benefits

Medical, dental, vision benefits

Flexible benefits

Job summary

Lilly in Indianapolis, Indiana, is launching a cutting-edge manufacturing site for advanced therapies. The Manufacturing Operator will support startup activities, coordinate with QA and maintenance, and perform routine GMP manufacturing across cell culture, purification, and fill/finish processes.

This role starts in the startup phase with day shifts and transitions to full operations. The position emphasizes strict adherence to GMP, quality documentation, and the use of digital systems, with

Qualifications

• Strong communication skills, both oral and written.
• Ability to work in a fast-paced team environment.
• Willingness to learn and follow GMP regulations and digital systems.
• Experience with manufacturing environments is preferred.

Responsibilities

• Work in a cleanroom environment to produce advanced therapies in a safe and quality manner.
• Coordinate production activities with Quality Control, Quality Assurance, and Plant Maintenance to facilitate on-time release of advanced therapies.
• Participate in equipment commissioning and qualification testing and process validation activities.
• Safely work with BSL-2 materials under the biologics safety program.
• Document production following batch records and SOPs.
• Maintain electronic records and logbooks per cGLP/cGMP.

Skills

Good communications

Team collaboration

Problem-solving

Attention to detail

Education

High School diploma or equivalent

Job description

Lilly in Indianapolis, Indiana, is launching a cutting-edge manufacturing site for advanced therapies. The Manufacturing Operator will support startup activities, coordinate with QA and maintenance, and perform routine GMP manufacturing across cell culture, purification, and fill/finish processes.

This role starts in the startup phase with day shifts and transitions to full operations. The position emphasizes strict adherence to GMP, quality documentation, and the use of digital systems, with