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Molecule Steward at Eli Lilly and Company - ApplyBlast

Molecule Steward

Eli Lilly and Company

3 months ago

4.0 on Glassdoor

Concord, NC

Onsite

Full Time

Senior

1 applicant

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About this role

The Site Molecule Steward serves as a technical subject matter expert for drug product manufacturing at the Concord site, providing scientific leadership and support for manufacturing operations. This role involves owning control strategy implementation, collaborating with cross-functional teams across the parenteral network, and offering technical direction on deviations and change controls. The position requires influencing technical capability building and ensuring strategies align with quality and regulatory guidance.

Responsibilities

Assume ownership of control strategy implementation and execution
Provide technical direction on deviations and production challenges
Collaborate with peers across the parenteral network
Support technical capability building and coaching at the site
Represent the TS/MS function in regulatory interactions

Skills

Qualifications

Bachelor's degree in science or engineering5 years in parenteral product manufacturing

About Eli Lilly and Company

lilly.com

Headquarters

Indianapolis, Indiana, United States

Company Size

10001+ employees

Founded

1876

View Profile

Eli Lilly and Company is a global biopharmaceutical company headquartered in Indianapolis, Indiana. It discovers, develops, manufactures and commercializes prescription medicines across therapeutic areas including diabetes, oncology, immunology, neuroscience and pain, and has a longstanding history in insulin and other major drug discoveries. Lilly invests heavily in research and clinical development and partners with biotech, academic institutions, and industry collaborators to advance biologics, small molecules, and precision medicines. The company operates global manufacturing and commercial networks and provides patient-support programs to improve access to its therapies.