Scientist, TS/MS - Device Assembly

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. This opportunity is at our new state‑of‑the‑art Parenteral, Device Assembly, and Packaging Facility in Concord, North Carolina. Organization Overview Lilly’s mission is to discover, develop, and deliver medicines that help people live longer, healthier, and more active lives. The company is a Fortune 500 leader with a 140‑year history of safety‑first, quality‑first, and ethical values. Responsibilities Support the Device Assembly Process Team as TS/MS representative. Serve as floor‑level technical interface for device components, equipment, and operations for the TSMS team. Provide technical support to non‑routine investigations, including consultation on quality and stability issues. Represent the Concord TSMS team for internal and external communications. Lead risk management activities as it pertains to product/process. Prepare and review relevant technical documents such as change controls, regulatory submissions, deviations, validations, protocols, procedures, PFDs, pFEMAs, etc. Develop, monitor, and react to statistically based metrics in real time to assess process variability and capability. Identify opportunities and lead technical projects to improve process control and/or productivity. Serve as interface with upstream suppliers and global device/drug product networks. Drive stability strategy for Concord products. Provide audit support as needed. Basic Requirements Bachelor’s or equivalent (Science or Engineering related degree preferred). 2+ years’ experience in a manufacturing organization. Additional Preferences Pharmaceutical and/or medical device manufacturing experience. Root cause investigation experience. Proven ability to work independently or as part of a team to resolve an issue. Strong attention to detail. Proficiency with computer systems including Microsoft Office, Veeva Vault, TrackWise, electronic batch records, and SAP. Knowledge and understanding of manufacturing processes. Strong interpersonal and teamwork skills. Strong self‑management and organizational skills. Additional Information Role is Monday through Friday. Flexibility to support production schedules, shutdowns, and other inputs is required. Occasional extended hours or off‑hour work may be required. Position will be based out of Concord, NC with ability to travel to Indianapolis and other Lilly sites as required. Compensation & Benefits Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage range for this position is $66,000–$171,600. Full‑time employees may also be eligible for a company bonus (dependent on company and individual performance). Lilly offers a comprehensive benefit program that includes a company‑sponsored 401(k), pension, vacation benefits, medical, dental, vision, prescription drug coverage, flexible benefits, life insurance, and well‑being benefits such as an employee assistance program, fitness benefits, and employee clubs. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. #J-18808-Ljbffr BioSpace