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 position is responsible for working with the Contract Manufacturer(s) (CM) to support supply, quality, and continuous process improvement of delivery devices, sub-assemblies, and components that are supplied to Lilly packaging and manufacturing sites.
Responsibilities

• Facilitate the Joint Process Team between Lilly and the Contract Manufacturer
• Supervise and communicate monthly JPT metrics
• Foster and support strong Safety and Quality Cultures at the CMs
• Provide day to day oversight of activities and resolve issues occurring between the CMs and Lilly sites
• Lead the resolution of manufacturing related issues, including deviations, evaluation of manufacturing data and supply chain daily/weekly issues
• Trained to perform TrackWise activities such as Lead investigator and Change Owner
• Provide operations project management input and oversight for capital projects at CMs
• Work with engineering, product stewards and others in the development/leading of process/product improvements. This may include project planning activities, development of protocols, coordination of internal and external lab based testing, documentation of the data and completion of technical reports
• Track completion of documentation and process updates resulting from local and global procedural changes, audits, complaint investigations, documentation reviews, product reviews, process reviews and equipment reviews
• Develop effective and productive working relationships with colleagues at CM sites
• Lead multi-functional/cross-site/cross-company project teams as needed
• Provide backup, as appropriate, for the Manager – CMO Operations

Basic Qualifications

• Bachelor’s Degree required
• 2 or more years manufacturing experience preferred
• Demonstrated high degree of ownership / accountability
• Strong communication (written and oral) skills, teamwork, and influence
• Solid technical writing skills
• Ability to organize and prioritize multiple tasks

Additional Preferences

• Previous Leadership/supervisory experience
• Career interest in operations or functional leadership
• Previous engineering or project management experience in medical devices

Other Information

• Travel required for CM (25%-100%) with possible 6 month STA.
• This position is planned to support US Reach CMs

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