Senior Scientist - TSMS

Job ID: R-110862Company: LillyLocation: Indianapolis, Indiana, United States of AmericaJob Type: Full TimeCategory: Manufacturing/QualityPosted Date: 2026-08-28At 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. Organization Overview:Join the energetic and growing Active Pharmaceutical Ingredient - External Manufacturing Organization (API-EM) that delivers a diverse portfolio of medicines essential to our patients around the world. The API EM TS/MS Sr. Scientist will provide technical and scientific expertise within a dynamic external manufacturing environment. The Sr. Scientist is responsible for providing technical support to achieve the reliable and compliant manufacture of API drug substance at external contract manufacturing groups to predetermined global quality standards. This person interacts daily with a wide variety of people, primarily external partners team members and site management.The candidate will be responsible for process monitoring, response to issues, and improvements where necessary. A strong understanding of manufacturing principles and Lilly systems is required to ensure those same standards are applied to the external contract manufacturers.The position requires knowledge of cGMPs, applicable global regulatory manufacturing guidance, and the corporate/industry standards. The position requires working cross-functionally within the site and other functions to deliver on technical objectives.Key Objectives/Deliverables:Provide technical oversight and stewardship for peptide manufacturing processes.Leads resolution of technical issues including those related to control strategy and manufacturing.Employ excellent communication skills to manage internal and external relationships.Build and maintain relationships with development and central technical organizations.Ensure proper characterization of processes and products and ensure effective documentation of the process description, measures, acceptable ranges, and specifications (and the justification of these measures, acceptable ranges, and specifications).Ensure that processes are compliant, capable, in control, and maintained in a validated or qualified state.Understand, justify and document the state of validation with data that evaluate the capability of the manufacturing process to meet its stated purpose.Influence and implement the network technical agenda and drive continuous improvement.Maintaining peptide processes in a state of compliance with US and global regulationsUnderstanding the scientific principles required for manufacturing intermediates and drug substances, including the interaction of chemistry and equipment.Operate with ‘Team Lilly’ in mind - including coaching and mentoring of peers and other scientists.Basic Requirements:Bachelors in scientific disciplines of Chemistry, Biochemistry, Biology, Pharmacy, or Engineering (Chemistry/Biochemistry strongly preferred)3+ years of demonstrated experience and proficiency with pharmaceutical manufacturing and working knowledge of regulatory expectations.Additional Preferences:Knowledge and experience with Regulatory requirementsKnowledge of data management practices across manufacturingEnthusiasm for changes, team spirit and flexibilityAbility to influence and communicate to diverse groups on business, or technical issues within the site and functionProficiency in delivering complex tasks and/or tasks that are cross-functionalDemonstrated Project Management skills and ability to coordinate complex projectsAdditional InformationSome travel (<25%) is requiredSome off-shift work (night/weekend) may be required to support 24/7 operationsQualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status).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.Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (View email address on click.appcast.io), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is$66,000 - $171,600Full-time equivalent employees also will 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 eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for 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.#WeAreLillySkillspharmaceutical manufacturingcgmp compliancepeptide manufacturingprocess validationprocess monitoringtechnical issue resolutionregulatory manufacturing guidancecross-functional collaborationproject managementdata managementdocumentationchemistrybiochemistrybiologypharmacyengineeringcoaching and mentoringcontinuous improvementstewardship