Director, Analytical Chemistry – Genetic Medicines; Analytical Development - BR&D

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 Overview:The Bioproduct Research and Development (BR&D) organization delivers new medicines to patients through the development and commercialization of insulins, peptides, oligonucleotides, monoclonal antibodies, novel therapeutic proteins, and genetic medicines systems. BR&D is a multidisciplinary group with deep technical expertise that works collaboratively with our discovery and manufacturing colleagues. Located in Indianapolis, IN, scientists have full access to Lilly’s deep pharmaceutical development expertise and engineering capabilities.  In this role, we are seeking experienced, innovative, and motivated candidates to apply their strong foundation in analytical sciences and experience in pharmaceutical development to enable clinical trials, regulatory submissions, and new product commercialization.  This role sits at the intersection of late-phase analytical execution and cross-functional control strategy leadership, operating in one of the most scientifically complex and rapidly evolving therapeutic areas in our pipeline.Position Responsibilities:Possess prior experience leading analytical efforts focused on genetic medicine (e.g., AAV-based gene therapy, gene editing, cell-based gene therapy, and RNA-based therapies) drug substance and drug product development and commercialization, as well as demonstrate familiarity with applicable regulatory requirements and emerging trends in the industry.Demonstrate a depth of knowledge in concepts relevant to genetic medicine drug substance and drug product commercialization, including developing analytical methods, justifying specifications, designing stability studies, authoring regulatory submissions, and addressing questions from global regulatory agencies.Drive the implementation of technical solutions and analytical strategies to enable process development and product understanding, delivering robust control strategies for genetic medicine drug substance and drug products. Collaborate within project teams, partner organizations, and across Discovery, Development, and Manufacturing to deliver material and information for clinical trials and regulatory submissions.Have experience authoring IND/CTA, BLA/NDA/MAA, and country-specific Response to Questions (RtQ). Monitor and assess emerging regulatory guidance and precedents to proactively shape Lilly's regulatory strategy for ATMP programs.Provide technical guidance for analytical activities executed within the external network. Ensure methods are technically sound, well developed and fit-for-purpose. Execute technology transfer to CRO/CMO organizations and Lilly manufacturing sites.Demonstrate high learning agility and the ability to understand and exploit effective scientific concepts and methods across multiple subject areas. Drive adoption of fit-for-purpose and novel analytical technologies that strengthen control strategy robustness for genetic medicine programs.Embrace diverse thought, background, and experience, and actively engage with the external environment to recognize and apply external innovation across the Lilly genetic medicine portfolio.Ensure continued technical and professional growth of group members, encourage efforts towards excellence and knowledge sharing.Plan and manage short-term and long-term development activities including developing/reviewing technical agendas and timelines for project work. Recommend resource allocation to accomplish projects according to plans, communicate progress and propose changes in timeline, objectives, or direction.Possess strong communication (oral, written), organizational, and leadership skills.Basic Qualifications:Ph.D. in Analytical Chemistry, Molecular Biology, Biochemistry, or Biology with 5+ years of experience in the pharmaceutical industry after earning degree; orM.S. in Analytical Chemistry, Molecular Biology, Biochemistry, or Biology; with 10+ years of relevant pharmaceutical or biotech industry experience; orB.S. in Analytical Chemistry, Molecular Biology, Biochemistry, or Biology; with 15+ years of relevant pharmaceutical or biotech industry experience.Demonstrated experience with analytical control strategy development for late-phase genetic medicine drug substances and drug products is required in a pharmaceutical or biotech development context.Prior experience developing global regulatory strategies including authoring regulatory submissions, responding to regulatory questions, and/or registering products across global markets in a pharmaceutical or biotech development context.Experience with technical transfer of analytical methods into internal or external GMP manufacturing facilities in a pharmaceutical or biotech development context.Additional Skills/Preferences:Strong technical depth that translates scientific innovation into measurable business value and a forward-looking approach to shaping future work plans.Proven experience managing complex technical projects from planning through delivery.Demonstrated leadership in collaborative, cross-functional team environments, with the ability to drive change and adapt quickly in a dynamic environment.Strong persuasion, influencing, and negotiation skills.Excellent interpersonal skills with a consistent orientation toward collaboration and fostering a positive, inclusive work environment.Ability to prioritize competing demands and operate effectively amid ambiguity.Additional Information:Travel: 0 to 15%Potential expo