Gene Therapy Drug Product Scientist – TS/MS (Startup)

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

Benefits offered by this job

Company bonus

Medical, dental, vision benefits

401(k)

Job summary

Lilly, headquartered in Indianapolis, IN, is seeking a Drug Product Manufacturing Scientist – TS/MS to support final formulation, parenteral manufacturing, and visual inspection of gene therapy products at a cutting-edge Lebanon, Indiana site.

You will join a team responsible for tech transfer, process validation, and regulatory documentation, guiding startup through validation and commercial production with a focus on quality and safety.

Qualifications

• Bachelor-level degree in a chemical engineering, biochemical engineering, chemistry, biochemistry or related field.
• 3+ years in parenteral or sterile drug product manufacturing, including formulation, aseptic fill-finish, visual inspection or packaging.
• 3+ years in cGMP manufacturing with exposure to drug product operations.

Responsibilities

• Provide technical support for drug product operations including tech transfer and process validation.
• Oversee formulation buffer/excipient preparation and visual inspection activities.
• Develop and review technical documents such as change controls, protocols, and reports.
• Lead or support cross-functional TS/MS projects to ensure startup success and process improvements.
• Monitor metrics to assess process variability and capability.
• Interface with Lebanon site and support audit activities.

Skills

Parenteral manufacturing

Aseptic processing

cGMP awareness

Drug product formulation

Education

B.S. in Chemical Engineering or related field

Tools

Filling equipment

Isolator technology

Serialization systems

Job description

Lilly, headquartered in Indianapolis, IN, is seeking a Drug Product Manufacturing Scientist – TS/MS to support final formulation, parenteral manufacturing, and visual inspection of gene therapy products at a cutting-edge Lebanon, Indiana site.

You will join a team responsible for tech transfer, process validation, and regulatory documentation, guiding startup through validation and commercial production with a focus on quality and safety.