Parenteral Operations Senior Director — Global Impact

Eli Lilly and Company; Pleasant Prairie (WI); On-site; USD 168,000 - 246,000; Full time

Benefits offered by this job

Bonus potential

401(k) plan

Medical, dental, vision benefits

Well-being programs

Job summary

Lilly in Wisconsin is seeking a Sr. Director, Parenteral Operations to lead the Parenteral Flow Team and ensure safety, quality and operational excellence in manufacturing. You will work with cross-functional groups to align on strategy and deliverables in a GMP environment.

The role reports to the Site Head, contributes to site planning, and mentors a diverse team while driving continuous improvement and regulatory compliance in parenteral production.

Qualifications

• Bachelor's degree in Engineering, Life Science, or Business/Operations.
• At least 10 years of experience at a pharmaceutical manufacturing site.
• At least 5 years of previous management or cross-functional leadership.
• Strong leadership, interpersonal and communication skills.
• Experience supervising cross-functional teams within Parenteral production.
• Solid understanding of FDA, EMEA, OSHA, and EPA requirements.
• Commitment to safety and adherence to HSE goals.

Responsibilities

• Lead Parenteral Flow Team and ensure safety, quality and efficiency.
• Develop and implement site strategic and business plans.
• Provide leadership and development to direct reports and team members.
• Maintain a state of control for resources and processes used in medicine production.
• Collaborate with Regulatory agencies during site inspections.
• Drive continuous improvement and Lean/OSSCE initiatives.

Skills

Leadership

Interpersonal skills

Cross-functional leadership

Regulatory awareness

Safety culture

Education

Bachelor's Degree in Engineering/Life Science/Business

Job description

Lilly in Wisconsin is seeking a Sr. Director, Parenteral Operations to lead the Parenteral Flow Team and ensure safety, quality and operational excellence in manufacturing. You will work with cross-functional groups to align on strategy and deliverables in a GMP environment.

The role reports to the Site Head, contributes to site planning, and mentors a diverse team while driving continuous improvement and regulatory compliance in parenteral production.