Senior Director - Parenteral Operations

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 Parenteral Operations Sr. Director is responsible for providing leadership to the cross-functional Process Teams and Flow Teams supporting the parenteral production areas. Utilizing the various teams and functions as described in the Manufacturing Standards for Operational Excellence (MSOEs) to ensure that all people, processes, facilities, and equipment are capable and compliant with the requirements of GMPs, OSHA, and any process and practice designated by the company site or plant as necessary in executing or supporting the making of medicine for our patients.

The Parenteral Operations Sr. Director will be reporting to the Site Head and is a member of the Kenosha Site Lead Team.

• Active member of the Kenosha Site Lead Team ensuring safety, quality, and operational excellence.
• Participate in the development and implementation of site strategic and business plans.
• Lead the Parenteral Flow Team, in accordance with the Manufacturing Standards for Operational Excellence.
• Provide leadership and development to direct reports and members of the Flow Lead Team and be a resource to mentor and coach others as circumstances require.
• Meet performance objectives established for the area of responsibility.
• Responsible for maintaining a safe work environment, leading safety initiatives, and working safely and accountable for supporting all HSE Corporate and Site Goals.
• Make medicine safely.
• Make medicine within all quality and compliance guidelines that pharma operations are subject to.
• Ensure that the area is capable in respect to key corporate best practices including, but not limited to OSSCE, CAPA, and Lean.
• Support site commercialization and new molecule pipeline plan.
• Understand and participate in the design of the manufacturing control strategy for formulation, filling, visual inspection Understand process variability.
• Achieve and maintain a state of control for resources and processes used in the making of medicine.
• Ensure that occasions when resources or processes are not capable, compliant, or in control are identified, investigated, and corrected.
• Where possible and consistent with business needs and objectives, take action to reduce variability and continuously improve performance within the area of responsibility.
• Partner with the Operational Excellence/Continuous Improvement organization in the delivery of MSOE training / education programs and drive Operational Excellence in day-to-day management of the operation.
• Lead and / or facilitate the implementation of projects and initiatives as identified and sanctioned by the site.
• Work with external parties such as Regulatory Agencies during site inspections, other Lilly Parenteral Network Sites, etc.
• Utilizing OSSCE, meet patents and other customer supply demands.
• Make the workplace more productive by taking advantage of diversity, inclusion, and engagement.

• Bachelor's Degree in Engineering, a Life Science, or Business/Operations
• At least 10 years of experience at a pharmaceutical manufacturing site
• At least 5…