PRD - Early Phase QA - Advisor/Sr. Advisor

Company: Eli Lilly and Company
Location: Indianapolis
Posted on: January 3, 2026

Job Description:

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. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. About the Job 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. Our employees around the world work to discover and bring life changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Position Brand Description: Early Phase Quality Assurance is accountable for GMP Quality dedicated to the PR&D Early Phase Team. This position is responsible for providing technical leadership to the Early Phase Quality Unit and as well as providing day to day Quality oversight to the Early Phase teams and external partners in support of executing the portfolio of both early phase development assets within PR&D, SMDD and BRD. Key Objectives/Deliverables: Support delivery of early phase Pre-Commercialization Information and Materials within the Early Phase portfolio (typically through Phase II); ensuring quality expectations/requirements are consistently met. Ensure appropriate execution of the Early Phase Quality System to sustain compliance with regulatory requirements and good manufacturing practices Review and approve manufacturing documentation Disposition API, in-process materials, dosage forms and finished drug product to be used in Clinical Trials including management and review of GMP documentation, analytical results and regulatory commitments. Coordinate deviation and complaint investigations, as needed Review and approve deviations, change documents, and specifications for Early Phase materials Provide QA input to CM&C Development Plans as part of Early Phase deliverables. Ensure contract manufacturers and packagers, testing laboratories, vendors, and suppliers are qualified to assure compliance and integrity of the supply chain and oversee partner activities within a manner that optimizes compliance as well as efficiency. Collaborate with internal business and quality partners (SMDD, BR&D, PD, ELECTS) to ensure appropriate Lilly oversight of Early Phase activities at external partners Maintain and execute a Quality System aligned with LQS, GQS, and PR&D QS commensurate with Early Phase scope and phase of development. Provide on-site support at partners/CMO’s for manufacturing, packaging and labeling activities of investigational medicinal products, and materials used to produce IMPs as necessary. Provide on-site support for internal manufacturing, packaging, labeling and distribution activities of investigational medicinal products, and materials used to produce IMPs as necessary. Identify opportunities for, and participate in, continuous improvement Ensure inspection readiness through site self-assessments, GMP education, monitoring, establishing and enhancing Quality systems and provide support for internal and regulatory site inspections Influence PR&D QA management via identification and/or implementation of process improvement opportunities for external party governance within PR&D Early Phase. Actively monitor changes to global compliance environment, and industry developments, assess impact/compliance of Early Phase Quality system and quality strategy, and implement necessary changes. Mentor, coach and develop Early Phase QA Team Members. Minimum Requirements: Demonstrated relevant experience in global clinical trial cGMP regulations Breadth of technical and quality knowledge including API, drug product manufacturing, clinical trial packaging, analytical laboratories. Demonstrated expertise of cGMP and Quality Systems with a minimum of 5 years internal Lilly and external experience in any of QA, QC, Manufacturing MS&T, or Regulatory Ability to interpret/apply phase-appropriate GMP standards Proficiency with applicable computer systems. Demonstrated strong oral and written communication skills. Critical thinking and technical problem-solving skills, including root cause analysis/troubleshooting skills. Demonstrated attention to detail. Additional Preferences: Proven ability to work independently or as part of a team to resolve an issue. Previous experience in QA, QC, Operations, TS/MS, Engineering, or Regulatory is desirable. Knowledge of PR&D Quality Systems and/or CT Operations is preferred Experience in cGMP Auditing Education Requirements: Bachelor’s degree in Science-related field or Engineering, or equivalent years of experience. Other Information: Travel US and OUS (including India and China) is required (15-25%) for collaboration partner oversight, training, conferences, etc. 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 ( https://careers.lilly.com/us/en/workplace-accommodation ) 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 Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $126,000 - $204,600 Full-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. WeAreLilly

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