Role Summary
Associate Director – Biologics Operations – Lilly Medicine Foundry. Directly responsible for managing day-to-day manufacturing operations in the Biologics building, overseeing operational resources for the execution team, and leading frontline leaders to safely and compliantly manufacture high-quality medicine. Acts as the key integrator of the cross-functional team to drive safety, quality, and continuous improvement in pursuit of Operational Excellence. Supports project delivery and startup phases with systems, processes, and staffing to enable GMP operations.
Responsibilities
- Build and promote a strong Safety and Quality culture; maintain a safe working environment and conduct production activities to protect safety, environment, and quality.
- Ensure consistency of operations across shifts through active engagement on the production floor.
- Own the implementation of the change and improvement agenda for the assigned area, ensuring cross-functional support and integration.
- Set objectives and development plans for Operations staff, including Operations Leaders and Operators.
- Manage events, ensuring appropriate communication within the team and with external teams; provide input and approve investigations.
- Ensure team members are appropriately trained, and that operating procedures and training material are available and current.
- Ensure regulatory compliance and operational excellence by supporting lean principles.
- Participate in development and delivery of the medium- and long-term strategic direction for the site.
- Ensure Biologics operations remain compliant with applicable regulatory requirements (Safety, Quality/cGMP, Environmental, Financial, Legal, HR).
- Support site governance through participation, influence and leadership in cross-functional meetings and initiatives.
Qualifications
- Required: Minimum of a bachelor's degree in a relevant scientific, engineering or operations discipline and a minimum of 5 years of experience in a leadership role managing operations or relevant experience within the pharmaceutical industry.
- Preferred: Ability to work with a team, make independent decisions, influence diverse groups; strong interpersonal skills; ability to provide innovative solutions and leverage ideas from other functional areas; strong verbal and written communication; ability to function in a cross-functional team environment as a leader.
Skills
- Leadership and people development
- Safety, quality, and regulatory compliance
- Operational excellence and lean principles
- Cross-functional collaboration and stakeholder management
- Process improvement and change management
Education
- Bachelor’s degree in a relevant scientific, engineering, or operations discipline
Additional Requirements
- Initial location at Lilly Technology Center, Indianapolis; permanent location at the Lilly Medicine Foundry in Lebanon, Indiana.
- Experience or ability to contribute during startup phase (2025–2027) including talent acquisition and building organizational capability to operate at high safety, quality, and operational excellence standards.