Peptide Manufacturing Science Leader

Eli Lilly and Company; Indianapolis (IN); On-site; USD 123,000 - 180,400; Full time

Benefits offered by this job

Comprehensive benefit program

Company bonus

401(k) and pension benefits

Vacation benefits

Medical, dental, and vision benefits

Job summary

Eli Lilly and Company is seeking an experienced Associate Director for their Technical Services team in Indianapolis, Indiana. This role focuses on providing critical technical leadership and expertise in peptide manufacturing processes to ensure compliance and optimize production.

Qualified candidates should have a B.S. in a relevant field and 8+ years in the pharmaceutical or biotechnology industry. Key responsibilities include leading a team, overseeing process validations, and collaborating with various departments to drive continuous improvement.

Qualifications

• 8+ years of relevant experience in manufacturing within the pharmaceutical or biotechnology industry.
• Proven leadership experience, including direct supervision and mentorship of scientific and technical staff.

Responsibilities

• Lead and manage a team of scientists to achieve departmental goals.
• Serve as the primary technical leader for peptide manufacturing processes.
• Oversee the transfer of new peptide processes from development to manufacturing.
• Design and execute experiments to optimize peptide manufacturing processes.
• Collaborate cross-functionally with R&D, Quality, and Manufacturing teams.
• Present technical findings to senior leadership.

Skills

Leadership

Analytical skills

Problem-solving

Communication

Education

B.S. in Chemistry, Biochemistry, Chemical Engineering, or related discipline

Job description

Eli Lilly and Company is seeking an experienced Associate Director for their Technical Services team in Indianapolis, Indiana. This role focuses on providing critical technical leadership and expertise in peptide manufacturing processes to ensure compliance and optimize production.

Qualified candidates should have a B.S. in a relevant field and 8+ years in the pharmaceutical or biotechnology industry. Key responsibilities include leading a team, overseeing process validations, and collaborating with various departments to drive continuous improvement.