Peptide Process Scientist

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Job description

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.

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 35,000 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.

Lilly is currently constructing an advanced manufacturing facility for production of API molecules located in Lebanon, IN. This facility is Lilly's largest investment in manufacturing capacity and is intended to provide APIs for current and future products. This is a unique opportunity to be a part of the leadership team for the startup of a greenfield manufacturing site, and the successful candidate will help to build the organization, the facility and the culture to enable a successful startup into GMP manufacturing operations.

Main Purpose and Objectives:

Lilly is seeking a peptide process scientist to join its Lebanon API TS/MS (Technical Services/Manufacturing Science) team. This position is responsible for designing and executing lab experimentation aimed to transfer processes, characterize processes, troubleshoot process upsets, and provide recommendations for process improvements for peptide manufacturing processes.

The TS/MS Process Scientist is part of the Lilly Lebanon API TS/MS laboratory team. This position will be peptide focused and will require interaction with Quality Assurance, Quality Control, Procurement, Warehouse, Regulatory departments, and other Lilly sites. Knowledge of chemistry and understand the scientific principles required for the manufacturing and testing of intermediates and bulk drug substances is required. Knowledge of organic synthesis and experience in peptide manufacturing are a plus. Knowledge of small molecule synthesis is a plus.

Key Responsibilities:

• Complete laboratory experimentation aimed at achieving the successful process development and transfer
• Developing experimental studies to address process upsets in routine manufacturing
• Design and perform range finding studies to enable effective process characterization
• Identify potential for process optimization to improve yield and throughput
• Coordinate with TS/MS team to setup models to support manufacturing as required.
• Accurately record data in accordance with TS/MS laboratory procedures
• Adhere to all Environmental, Health, and Safety standards.
• Effective management of multiple projects.
• Utilize technical skills to lead or perform in-depth investigations for out of specification results and aberrant data. Draw conclusions and perform root cause analysis investigations and recommend solutions to prevent reoccurrence.
• Communicate effectively in both written and oral formats.
• Participate in internal/external audits as needed.

Basic Requirements:

• Bachelor degree (4 year College) in a science field related to the lab (e.g. Chemistry, Biochemistry, Pharmaceutical Science). Advanced degree (MS or PhD) preferred but not required.

Additional Preferences:

• Excellent communication skills, both oral and written.
• Ability to independently master assigned processes and to coordinate activities with internal and external partners.
• Advanced science degree.
• Experience with peptide pharmaceutical development and characterization.
• Experience in API manufacturing.
• An understanding of cGMP and regulatory requirements.
• Experience with continuous processing is a plus
• Experience with process characterization is a plus
• Experience transferring processes into GMP manufacturing is a plus

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities. Learn more about all of our groups.

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