Associate Director
3 months ago
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.
Organization Overview:
Indianapolis Parenteral Manufacturing (IPM) manufactures, fills, and inspects sterile injectable medicines with safety first and quality always. This role will lead the Engineering organization for a filling, formulation, or inspection manufacturing process within the site. Reports to this role include primary and secondary loop Process Engineers, Automation Engineers, and technicians supporting the designated manufacturing process.
Key Objectives/Deliverables:
Work safely and continually look for improvements to both people and equipment safety.
Provide site engineering leadership of safety, quality and continuous improvement as well develop best practices and standards to support manufacturing and reliability.
Develop, mentor, coach and recognize their team
Implement business plan objectives
Own the reliability program supporting the manufacturing process to eliminate unplanned downtime and ensure the supply of medicine.
Support regulatory inspections, Data Integrity initiatives, and overall continuous improvement of quality systems.
Own and improve processes associated with project management, financial planning, shutdown coordination, commissioning and verification, and project startups.
Minimum Requirements:
Bachelors Degree in Engineering required.
Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.
Recognized strong team leadership skills
Strong problem-solving and analytical skills
Ability to communicate effectively at all levels (both oral and written)
Strong talent development skills, especially coaching and people development
Solid regulatory compliance knowledge (GMP, OSHA, etc.)
Understanding of reliability and project management principles
Additional Preferences:
Previous supervisory/leadership experience
Experience with regulatory inspections
Previous pharmaceutical experience, preferably Parenteral Manufacturing
Other Information:
Occasional travel may be required.
Off-hours work and phone calls may be required.
Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly_Recruiting_Compliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.
Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.
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