Sr. Principal Scientist - TS/MS - Eli Lilly and Company : Job Details

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

Organization Overview:

The TS/MS Parenteral Pilot Plant is a group of skilled engineers and scientists who possess deep technical expertise in the manufacture of parenteral products. The pilot plant partners with site process engineers, TS/MS scientists, and development engineers and scientists to drive process improvements, troubleshoot process issues, evaluate new technologies, and ensure compliance with quality standards.

Responsibilities:

• Collaborate with cross-functional teams in manufacturing and development to troubleshoot process issues, scale-up new development processes, aid in technology transfer, and evaluate new technologies.
• Partner with development scientists and engineers to develop process operations and manufacturability of different molecules and platforms.
• Partner with manufacturing sites (internal and external) to solve current manufacturing issues and work on long term solutions. Lead and support efforts to drive optimization and reliability of unit operations.
• Participate in technology transfer activities from development to commercial site or between commercial sites, ensuring successful scale-up and process validation.
• Prepare study protocols and tickets that align with pilot plant processes and procedures to meet customer needs.
• Actively seek and engage in discussions and decisions regarding emerging technologies that may be applied to develop and control processes.
• Prepare technical reports and summary packages as necessary to ensure appropriate retrievable documentation of study conclusions.

Basic Requirements:

• Bachelor of Science Degree in Chemical Engineering or degree in scientific field with good understanding of engineering first principles.
• Minimum 5+ years of experience in parenteral manufacturing, pilot plants, or process development.
• Fluent in written and spoken English.

Additional Skills/Preferences:

• Understand regulatory requirements.
• Ability to work well independently and in teams.
• Experience with isolator technologies.
• Understanding of statistical concepts and experimental design.

Additional Information:

• The position is based out of Greenfield, IN.
• Flexible schedule as some activities may require occasional support outside normal hours.
• Ability to travel (< 10%) supporting US and OUS projects.
• Business title will vary depending on level.