Sr. Director - BRD Analytical Development

Eli Lilly and • Indianapolis, IN

75d • $151,500 - $222,200

About The Position

This leadership role within the Bioproduct Research & Development (BRD) organization is responsible for managing a team of technical experts focused on developing and executing comprehensive analytical strategies to support a diverse portfolio of bioproducts. These include antibodies, proteins, cell and gene therapies (CGT), non-viral gene delivery platforms, parenterally administered synthetic peptides and oligonucleotides, and their conjugates. The role encompasses accountability for pipeline project delivery, scientific and technological advancement, talent development, organizational growth, and execution of functional strategy. The incumbent ensures robust systems and a well-trained workforce-including internal staff, insourced personnel, and external partners-are in place to meet pipeline demands. Any GMP testing laboratories under this leader's oversight must maintain a state of continuous inspection readiness and full compliance with applicable regulatory guidelines, including ICH Q-series and 21 CFR Parts 11, 210, and 211.

Requirements

• Ph.D. in Biology, Chemistry, Pharmacy, or a related life science discipline is strongly preferred.
• Minimum of 8 years of relevant pharmaceutical industry experience.
• Strong communication, interpersonal, and leadership skills.
• Solid understanding of Good Manufacturing Practices (GMPs) and the drug development lifecycle.

Responsibilities

• Lead a team of scientists in phase-appropriate analytical development from preclinical stages through commercialization.
• Align integrated development plans across key functions (Drug Substance, Drug Product) and interfaces (device, discovery, manufacturing, quality).
• Set and implement strategic direction for science, technology, and business operations to support pipeline delivery and organizational goals.
• Allocate resources and assign personnel to new projects based on scope and priority.
• Monitor project progress, ensure timely execution, and mobilize resources to address technical challenges.
• Oversee laboratory operations with a strong emphasis on safety, compliance, and inspection readiness.
• Ensure the team remains current with scientific advancements, emerging technologies, and evolving regulatory requirements, and integrates them appropriately.
• Maintain compliance with all applicable laws, regulations, and industry standards governing drug development.
• Provide technical consultation to manufacturing sites as needed to support product development and troubleshooting.
• Foster a high-performance culture through effective performance management, coaching, mentoring, and career development; contribute to talent assessment and succession planning.
• Uphold and promote adherence to company policies and values.

Benefits

• 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.
• Well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Industry: Chemical Manufacturing
• Education Level: Ph.D. or professional degree