Manufacturing Documentation Coordinator

At Elanco (

NYSE:

ELAN) - it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People. At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights. Making animals' lives better makes life better - join our team today!

Your Role:

Manufacturing Documentation Coordinator As the Manufacturing Documentation Coordinator you'll partner with cross functional teams to ensure manufacturing documentation is effectively reviewed and forward processed downstream teams. You'll represent operations as a partner for quality and floor-operations document completion, and ensure the timely, effective submission of

Your Responsibilities:

Review manufacturing documentation for accuracy and completeness Coordinate updates to documentation as needed by floor operation staff Investigate and improve process inefficiencies to timely fulfillment of documentation Steward batch documentation lifecycle through operations, including chain-of-custody Support process teams through floor scheduling and documentation review Uphold strong safety and quality culture Support manufacturing through operational mentorship and technical coaching What You Need to Succeed (minimum qualifications):

Education:

High school Diploma or greater

Experience:

3 years of experience within GMP manufacturing Top 2

Skills:

Strong GMP documentation expertise combined with the ability to review, improve, and ensure accuracy of batch records, along with effective cross-functional collaboration to support manufacturing operations and resolve documentation issues. What will give you a competitive edge (preferred qualifications): Proven technical writing capability 3+ years experience within animal health pharmaceutical manufacturing SAP experience Familiarity with Veeva Cross-functional team work Strong coaching/mentorship skills Cradle to grave understanding of biologic manufacturing operations

Additional Information:

Travel:

occasional