Job Title
Senior Director, Global Regulatory Affairs CMC – Synthetic Molecules
Location
Indianapolis, Indiana, United States
Company
Eli Lilly and Company
Category
Research & Development
Job Type
Full Time | Regular
Job ID
R-82502
Position Summary
Eli Lilly is seeking a Senior Director for Global Regulatory Affairs CMC (GRA-CMC) to lead regulatory activities for global submissions related to synthetic molecules. This individual will manage the regulatory strategy for development and commercial products, supervise personnel, ensure on-time regulatory submission deliveries, and foster continuous improvement within the GRA-CMC organization. The Senior Director will provide scientific leadership and influence internal and external stakeholders while ensuring compliance with global CMC regulatory requirements.
Key Responsibilities
People Excellence - Supervision of Personnel:
Ensure staff have the necessary qualifications and align with leadership expectations.
Oversee recruitment and performance management for the team.
Develop and implement training curricula, ensuring appropriate resource allocation for projects.
Technical and Regulatory Functional Excellence:
Lead regulatory strategies and ensure they integrate scientific and technical principles.
Oversee preparation and finalization of CMC documents for global regulatory submissions (CTAs, MAAs, post-approval supplements).
Maintain knowledge of global CMC regulatory requirements and provide expertise to the team.
Oversight of CMC Project Deliverables:
Approve regulatory strategies for global CMC development and manufacturing changes.
Ensure on-time delivery of regulatory documents and manage submissions to health authorities.
Provide regulatory leadership and communicate strategies across teams to ensure compliance.
Internal and External Influence:
Mentor and influence internal teams, including cross-functional areas.
Participate in industry technical organizations and regulatory bodies to shape the external environment.
Influence internal governance committees and ensure departmental objectives are met.
Department Communications:
Stay informed of GRA initiatives and communicate information to the department.
Address and communicate issues to upper management as necessary.
Operational Excellence and Process Management:
Collaborate with other Senior Directors to evaluate and improve internal processes.
Ensure adherence to the Regulatory Quality System (RQS) and document key business practices.
Education Requirements
BS, MS, or PhD in Chemistry, Biology, Engineering, or a closely related science.
10+ years of experience in CMC development and/or technical support for commercial products.
3+ years of demonstrated team leadership experience.
Proven expertise in drug development, API, Drug Product, or Analytical areas.
Additional Skills/Preferences
In-depth knowledge of CMC regulatory experience.
Experience in synthetic molecule portfolio regulatory affairs.
Strong leadership, communication, and mentoring skills.
Familiarity with global regulatory processes and health authority interactions.
Compensation
Anticipated Salary Range: $162,000 – $237,600 annually.
Eligible for company bonus program (based on company and individual performance).
Benefits
401(k) plan and pension
Vacation and paid time off
Medical, dental, vision, and prescription drug benefits
Flexible spending accounts (healthcare, dependent care)
Life insurance and death benefits
Wellness programs (EAP, fitness benefits, clubs and activities)
Other leave of absence benefits
Travel
10-15% travel required.
On-Site Position
Located at Lilly Corporate Center in Indianapolis, Indiana.
Equal Opportunity Employer
Lilly is an equal opportunity employer dedicated to diversity and inclusion.
Employee Resource Groups (ERGs)
Includes groups such as Black Employees at Lilly, Organization of Latinx at Lilly (OLA), Lilly India Network, PRIDE (LGBTQ+ Allies), Women’s Initiative for Leading at Lilly (WILL), and others.
Accommodation
Applicants needing accommodations during the application process can request assistance via the Accommodation Request Form.
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