Director​/Senior Director, CMC, Drug Product Development

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.

The Director/Senior Director, CMC, Drug Product Development will lead formulation development activities across multiple dosage forms and therapeutic modalities, with a focus on developing and incorporating digital solutions and tools into drug product workflows. The ideal candidate will bring expertise in both parenteral and solid oral dosage forms, combined with emerging capabilities in computational and AI-driven formulation approaches. Success in this role requires cross‑function collaboration and leadership as well as a strategic vision for how technology can be leveraged to transform traditional drug development activities.

• Lead formulation design, development and external manufacturing for both parenteral (IV, SC, IM) and solid oral (tablets, capsules) drug products across diverse therapeutic programs and modalities.
• Develop robust formulation strategies that address in vivo performance, stability, bioavailability, manufacturability, and patient‑centric considerations.
• Manage a network of external providers (CROs, CDMOs) with capabilities in drug product development and manufacturing.
• Author CMC sections of regulatory submissions (IND, CTA) related to drug product development and manufacturing.
• Support regulatory interactions and respond to health authority questions.
• Ensure compliance with cGMP standards and ICH guidelines.

• Lead the development, testing and implementation of digital solutions related to drug product development.
• Partner with IT and other internal drug product subject matter experts to translate drug product workflows into requirements that can be incorporated into technology solutions.
• Lead the evaluation of in silico modeling tools and AI/ML platforms that predict formulation performance and accelerate development timelines.
• Continuously monitor the industry trends, competitive landscape and emerging technologies to identify future tools and technology platforms of interest.

• Education:
  
  PhD in Pharmaceutical Science or related field (Chemistry, Chemical Engineering, Pharmacy).
• 8+ years of pharmaceutical industry experience.
• 3+ years of prior experience with application of in silico tools or AI/ML solutions in drug product development.

• Experience working with multiple therapeutic modalities (small molecules, biologics, peptides, oligonucleotides).
• Experience with both parenteral and solid oral formulations.
• Knowledge of emerging modalities including cell & gene therapy, RNA‑based medicines.
• Strong analytical and problem‑solving skills.
• Experience working with biotechs/emerging companies and/or early‑stage development programs where speed to clinic is a critical success factor.
• Demonstrated ability to operate effectively in fast‑paced environments where rapid decision‑making and pragmatic problem‑solving are essential to maintain program momentum.
• Track record of supporting multiple concurrent programs with varying levels of technical maturity, demonstrating agility in shifting priorities and creative approaches to address emerging challenges.

• Remote options may be considered based on business needs.
• Travel up to 10%.

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