Lead - Manufacturing Operations Systems
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. The Manufacturing Operations Systems specialist role will report to an Associate Director of Packaging Operations. The Manufacturing Operations Systems specialist will be responsible for owning initiatives and process improvements, acting as a liaison between operations and multiple functional groups to support event management, change controls, etc. The Manufacturing Operations Systems specialist will also assist the operations team in the day to day management of the production floor and lead investigations and drive implementation of actions associated with deviations. Key Objectives/Deliverables: Support Site Leadership to build a capable site organization by delivering area operational procedures, quality processes and controls for the Packaging areas. Monitor and build a strong safety culture Ensure consistency of operations across shifts through active engagement on the shop floor and through Gemba walks and Practice vs. Procedure evaluations. Participates and/or lead cross functional teams in the development and implementation of strategies associated with the area for the following initiatives: Continuous Improvement, Root Cause Analysis (RCA), Failure Modes Effect Analysis (FMEA), Operational Standards for Supply Chain Excellence (OSSCE). Identify changes required for MES and ensure they are implemented consistently with operational practices. Work with EWM, IDS and Master Data Team to support launch and ticket builds Lead training and troubleshooting for operations. Work closely with Logistics on the release of orders Understand and influence the manufacturing control strategy for their area. Trained as a Deviation Investigator Development and monitoring of metrics for the area Aid in issue resolution, batch/product approvals, and production schedule execution. Lead specific activities of the process teams. Key Objectives/Deliverables:
Requirements
- High School Diploma or equivalent
- 2 to 5 years Operations or Manufacturing Support in Pharmaceuticals
- Understanding of basic requirements of regulatory agencies such as the FDA, EMEA, DEKRA, and OSHA
- Excellent interpersonal, written and oral communication skills
- Responsible for maintaining a safe work environment, working safely, and accountable for supporting all HSE Goals
- Must be flexible to attend meetings or support off-shifts (operations is 24/7)
- Ability to travel up to 10%
Nice To Haves
- Technical or Science degree preferred
- Experience with cGMP environment
- Experience with EWM and SAP environments and transactions
- Career interests in Operations Leadership
- Device Assembly or Packaging experience
Responsibilities
- Owning initiatives and process improvements
- Acting as a liaison between operations and multiple functional groups to support event management, change controls, etc
- Assist the operations team in the day to day management of the production floor
- Lead investigations and drive implementation of actions associated with deviations
- Support Site Leadership to build a capable site organization by delivering area operational procedures, quality processes and controls for the Packaging areas
- Monitor and build a strong safety culture
- Ensure consistency of operations across shifts through active engagement on the shop floor and through Gemba walks and Practice vs. Procedure evaluations
- Participates and/or lead cross functional teams in the development and implementation of strategies associated with the area for the following initiatives: Continuous Improvement, Root Cause Analysis (RCA), Failure Modes Effect Analysis (FMEA), Operational Standards for Supply Chain Excellence (OSSCE)
- Identify changes required for MES and ensure they are implemented consistently with operational practices
- Work with EWM, IDS and Master Data Team to support launch and ticket builds
- Lead training and troubleshooting for operations
- Work closely with Logistics on the release of orders
- Understand and influence the manufacturing control strategy for their area
- Trained as a Deviation Investigator
- Development and monitoring of metrics for the area
- Aid in issue resolution, batch/product approvals, and production schedule execution
- Lead specific activities of the process teams
Benefits
- Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance).
- Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for 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; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
Number of Employees
5,001-10,000 employees
