TSMS- Sr. Scientist

Senior Scientist - Technical Services/Manufacturing Sciences (TS/MS) Cleaning At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life‑changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. As our biologics pipeline continues to expand, Eli Lilly & Company has invested in a state‑of‑the‑art new facility in Richmond, VA. To support this exciting new GMP manufacturing facility and ensure a safe and successful start‑up, we are seeking talented individuals to contribute to establishing Lilly Richmond as a reliable supplier of our innovative medicines and furthering our goal of making a difference to people’s lives. The TS/MS Sr. Scientist is responsible for supporting the cleaning program for process equipment and ancillary components in the manufacturing facility. The role will provide technical support for introducing and supporting biologics manufacturing processes from start‑up through routine operations. Key Responsibilities Develop cleaning strategy in collaboration with Engineering and Quality counterparts for Lilly Limerick Monoclonal Facility Author and own the Cleaning Validation Master Plan for the facility Generate cleaning validation protocols and summary reports Execute cleaning validation protocols, including visual inspection and sampling and coordination with other support groups (e.g., operations, maintenance, lab, etc.) Author cleaning procedures and associated work instructions for all equipment Develop cleaning batch records or appropriate documents to enable execution of cleaning activities on the production floor Complete review of executed cleaning batch records/documentation Troubleshoot issues with and optimize cleaning cycles and/or cleaning equipment Provide technical support on cleaning deviations/events and assist in root cause analysis Complete changes associated with cleaning equipment, cleaning cycles and cleaning program Complete periodic review reports for key components to ensure cleaning equipment remains in a qualified state Basic Requirements BS in Biochemistry, Biotechnology, Chemical Engineering or related discipline A minimum of 3 years of experience within the biopharmaceutical or GMP industry Qualified applicants must be authorized to work in the United States on a full‑time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F‑1 CPT, F‑1 OPT, F‑1 STEM OPT, J‑1, H‑1B, TN, O‑1, E‑3, H‑1B1, or L‑1 Additional Preferences MS in Biochemistry, Biotechnology, Chemical Engineering or related discipline Technical knowledge of cleaning equipment (CIP skids, parts washers, etc.) and cleaning regimes (chemical, recirculated washing, etc.) Knowledge of qualification/validation requirements and good documentation practices Knowledge of biologics manufacturing processes and understanding of production schedules Strong written and verbal communication skills Ability to work on own initiative and as part of a process team consisting of a diverse group of management, production/science and engineering professionals Demonstrated technical capability with high productivity Self‑starter with high initiative and a data‑driven approach to problem‑solving Demonstrated strong interpersonal skills Demonstrated adaptability and flexibility to working in different environments and teams Work Environment Onsite 8‑hour day role. As a manufacturing support function, occasional evening or weekend support may be required 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 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. Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $79,500 – $171,600. Full‑time equivalent employees will also be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including participation in a company‑sponsored 401(k), pension, vacation benefits, medical, dental, vision and prescription drug benefits, flexible benefits (e.g., healthcare and/or dependent day‑care flexible spending accounts), life insurance and death benefits, certain time off and leave of absence benefits, and well‑being benefits (e.g., employee assistance program, fitness benefits and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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