Advisor/ Sr. Advisor - Regulatory CMC

100 Eli Lilly and Company; United States; Hybrid; USD 168,000 - 268,000; Full time

Benefits offered by this job

401(k) plan

Pension

Vacation benefits

Medical, dental, vision benefits

Job summary

Lilly in Indianapolis/Boston (hybrid) seeks a Regulatory Scientist to provide strategic CMC regulatory support for clinical trials, market registrations, and post-approval activities. The role requires strong cross-functional collaboration across research, development, manufacturing, and regulatory teams to ensure successful global submissions.

Expected to lead global CMC strategies, contribute to risk-based regulatory solutions, and mentor junior staff.

Qualifications

• Bachelor’s degree in sciences discipline; minimum of 5 years regulatory CMC experience in pharma/biotech.
• Strong written, spoken and presentation communication skills.
• Demonstrated negotiation and influence skills; attention to detail.
• Effective teamwork; able to adapt to diverse interpersonal styles.

Responsibilities

• Lead preparation, review, and finalization of global CMC submissions (CTAs, marketing applications, variations, responses to health authority questions).
• Provide high-quality regulatory advice to enable development, manufacturing, and lifecycle planning decisions.
• Develop and maintain global CMC regulatory strategies in response to evolving expectations.

Skills

CMC knowledge

Regulatory strategy

Cross-functional

Written communication

Submission content

Education

Bachelor's degree in sciences

Job description

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 purpose of the Advisor/Sr. Advisor - Global Regulatory Affairs (GRA) –CMC Platform Regulatory Scientist role is to provide strategic, tactical, and operational regulatory CMC support across therapeutic modalities and manufacturing technologies in support of clinical trials, market registrations, and post-approval activities. This role applies CMC technical knowledge and regulatory expertise to develop and execute sound global regulatory strategies, ensuring internal consistency, effective change management, and predictable regulatory outcomes. Success in this role requires building collegial and productive relationships across research, development, development, manufacturing, quality, regulatory, and partner organizations.

Location: Indianapolis or Boston (hybrid)

Regulatory & Scientific Expertise

• Apply strong technical knowledge of CMC drug development and pharmaceutical manufacturing sciences across drug substance, drug product, and analytical areas.
• Demonstrates broad knowledge of global CMC regulatory requirements and guidelines for conducting clinical trials, obtaining global product registrations, and maintaining approved registrations.
• Develops, implements, and maintains global CMC regulatory strategies in response to evolving regulatory expectations and program needs.
• Provides high-quality, timely regulatory advice to enable informed development, manufacturing, and lifecycle planning decisions.
• Evaluates the regulatory impact of proposed CMC development, manufacturing, or change strategies and identifies risks and mitigation options.
• Leads preparation, review, and finalization of CMC documents for global regulatory submissions, including clinical trial applications, marketing applications, variations/supplements, and responses to health authority questions.
• Anticipates and resolves technical or operational issues that could impact submission timing, regulatory compliance, or product supply.
• Independently manages technically challenging or complex issues and proposes practical, risk-based regulatory solutions.

Influence

• Build strong working relationships across Global Regulatory Affairs, research and development, manufacturing, quality, and regional/affiliate regulatory teams to drive alignment on CMC regulatory strategies.
• Provides regulatory guidance and subject matter expertise to CMC teams and stakeholders to support successful submissions and approvals.
• Exhibits strong leadership behaviors and is recognized as a trusted mentor and resource within the regulatory CMC community.
• Incorporates new regulations, guidance, and company positions into processes, tools, templates, and training materials to support consistent execution.
• Provides input into internal policy development and contributes to internal discussions on emerging global CMC regulatory trends.
• Participates in industry forums or working groups, as appropriate, to maintain awareness of evolving regulatory expectations.

Lead / Partner

• Leads or supports cross-functional teams in the development and execution of global CMC regulatory strategies.
• Takes an active role in the critical review of CMC development strategies, control strategies, and submission content to ensure regulatory robustness.
• Collaborate effectively with manufacturing sites, technical experts, and quality organizations to resolve regulatory issues and support timely delivery of commitments.
• Supports health authority interactions for CMC topics, including preparation of briefing materials and responses to questions, as appropriate.
• Communicate regulatory strategies, risks, and recommendations clearly and effectively to team members and stakeholders.
• Participates in forums that share regulatory knowledge, lessons learned, and best practices across the organization.
• Contributes to the development of corporate positions and responses to proposed agency regulations and guidelines relevant to CMC.

Basic Qualifications

Bachelor’s degree in sciences discipline (e.g. chemistry, biology, biochemistry, pharmacy or related scientific discipline) Minimum of 5 years regulatory CMC experience within pharma or biotech industry Additional Preferences 7 + years pharmaceutical industry experience in CMC technical drug development Prior experience authoring CMC submission content Demonstrated strong written, spoken and presentation communication skills. Demonstrated negotiation and influence skills. Demonstrated attention to detail. Demonstrated effective teamwork skills; able to adapt to diverse interpersonal styles.

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 (AMECA), Black Employees at Lilly (BE@Lilly), 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 $168,000 - $268,400 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 At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people. We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe! #WeAreLilly