Director, Global Regulatory Affairs - CMC, Lifecycle Innovation

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.

The Director, GRA-CMCD Lifecycle Innovation provides scientific, strategic, tactical and operational regulatory leadership for post-approval CMC activities across Lilly's parenteral product commercial portfolio.  This role leads complex global lifecycle regulatory strategies across products and manufacturing sites, enabling high-quality, timely execution of post-approval changes while improving submission efficiency and simplifying regulatory processes.

This is accomplished with a strong working knowledge of global regulations, guidelines, and regulatory precedence, coupled with a strong technical knowledge of development, technology transfers and manufacturing processes. The Director develops collegial and mutually productive relationships with regulatory peers, across Lilly components, partner company components, and global regulatory agency personnel - partnering closely with sites and cross-functional teams to ensure high-quality, timely execution of post-approval regulatory activities.

** Key Responsibilities*
* + Deep technical knowledge and understanding of CMC molecule drug development and manufacturing science(s); broad technical knowledge of global CMC regulatory requirements and guidelines for reporting post-approval changes and updating global product registrations.

+ Provide high-quality, timely, and decisive regulatory advice to allow project teams to make well-informed decisions on product lifecycle planning; anticipate and resolve technical or operational issues that could impact submission timing.

+ Serve as regulatory lead for site additions and technology transfers, managing regulatory relationships with Lilly sites and external contract manufacturing organizations (CMOs) to ensure alignment on data packages and submission timelines.

+ Develop and implement post-approval regulatory strategies for assigned products and sites, defining filing approaches and data expectations for site changes, analytical updates, specification changes, site additions, and related lifecycle activities.

+ Lead preparation, review, and execution of variations, supplements, annual reports, DMFs, and related submissions; review and approve CMC documents for global submissions, including manufacturing changes, annual reports, and renewals.

+ Lead regulatory assessments for change controls and deviations for assigned products/sites, applying risk-based principles to categorize and prioritize post-approval changes.

+ Work closely with Manufacturing and Quality to develop compliant and scientifically sound data packages; coordinate with sites to ensure readiness and alignment on regulatory expectations and timelines.

+ Monitor emerging regulatory guidance related to lifecycle management and apply it strategically to current and future submissions; identify opportunities to simplify lifecycle processes or accelerate submissions.

+ Network with GRA, M&Q, and Business Unit leadership, as appropriate, to build awareness and alignment on complex CMC regulatory strategies; serve as a regulatory point of contact for assigned manufacturing sites.

+ Contribute to implementation of digital tools supporting lifecycle management, including automated templates, digital submissions, and AI/ML applications. Experience or interest in digital enablement and process simplification is especially valued in this role.

+ Communicate lifecycle strategies, risks, and timelines clearly to sites and cross-functional partners; translate regulatory implications for operational and business stakeholders.

+ Supervision and/or mentoring of global regulatory affairs scientists, regulatory associates and teams as needed.

** Basic Qualifications/Requirements*
* + B.S. degree in a STEM field.

+ 7 + years of Regulatory CMC or technical CMC experience supporting post-approval lifecycle management of biologics, parenteral products, combination…