About the position
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. Lilly is entering an exciting period of growth, and we are committed to delivering innovative medicines to patients around the world. Lilly is investing over $300 Million to create a new state-of-the-art manufacturing site for Gene Therapy, in Lebanon, Indiana. The brand-new facility will utilize the latest technology for Gene Therapy Manufacturing and Technology. This is an exciting once-in-a-lifetime opportunity to help build and operate a new site. The Lilly Lebanon Advanced Therapeutic site will be built using the latest high-tech equipment, advanced highly integrated and automated manufacturing systems, and have a focus on minimizing the impact to our environment.
Responsibilities
- Collaborate with app developers to deliver functional apps within a specific time frame
- Translate business requirements and specifications into user stories and maintain the backlog
- Be a point of contact between the business and the TECH@Lilly development team to help identify priorities
- Help work across support when issues are identified and determine the impact
- Partner cross functionally locally and globally to deliver GMP based apps for the MES
- Influence the roadmap and provide input to the MES architecture based on business knowledge and expertise
Requirements
- Bachelor's Degree in IT, Engineering, or related technical field, or High School Diploma/GED with 5+ years IT leadership experience working in Pharma and Manufacturing and Quality, especially API Manufacturing or Gene Therapy manufacturing.
- 5+ years of strong experience with DevOPs and Product Ownership.
- Scrum Certification and/or Agile Certification
Nice-to-haves
- Experience with creating and maintaining user stories
- Experience with maintain a backlog and working in an agile framework
- Pharmaceutical Manufacturing Regulatory compliance knowledge and experience (GMP)
- Effective people and team leadership skills
- Ability to manage and contribute to multiple concurrent activities and adapt to changes in priorities.
- Ability to collaborate cross functionally
- Excellent written and oral communication skills.
- Demonstrate creativity, analytical thinking, and the ability to troubleshoot and solve problems.
- Knowledge of cloud solutions and architecture
- History of promoting safety and maintaining a safe work environment
- Establish a strong site culture based on Lilly values, expectations, and operational excellence standards.
- Demonstrated adherence to compliance for internal and external quality guidance.
- Demonstrated and promoted Operational Excellence
- Effectively encourage knowledge sharing and education
- Evaluate and translate functional requirements into technical solutions.
- Ability to solve problems and work through manufacturing situations. Have experience serving as an escalation contact with vendor(s)
Benefits
- 401(k)
- Pension
- Vacation benefits
- Medical, dental, vision and prescription drug benefits
- Flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
- Life insurance and death benefits
- Certain time off and leave of absence benefits
- Well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)
