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Quality Assurance Associate - Investigation CoordinatorElanco Animal Health • United States
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Quality Assurance Associate - Investigation Coordinator

Elanco Animal Health
  • US
    United States
  • US
    United States
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Quality Assurance Associate – Investigation Coordinator
At Elanco – 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: Quality Assurance Associate – Investigation Coordinator As the Quality Assurance Associate – Investigation Coordinator, you'll partner cross-functionally with Manufacturing, Warehouse, Facilities, Quality Control, and Quality Assurance teams to support and oversee the site deviation and investigation management processes. You'll help drive investigations, root cause analysis, and corrective actions to timely closure while ensuring compliance with GMP and regulatory expectations. This role serves as a key partner in maintaining site quality standards, supporting continuous improvement initiatives, and strengthening operational compliance across the facility. Your Responsibilities: Coordinate and oversee daily activities within the site deviation management system Lead and support deviation investigations to timely and compliant closure Facilitate or support Deviation Review Board (DRB) activities and cross-functional collaboration Drive and coach root cause analysis (RCA) activities using tools such as 5 Whys and Ishikawa/6M Ensure appropriate CAPAs are identified and implemented to reduce recurrence of deviations Communicate investigation status updates and timelines across departments Lead or assist customer complaint investigations as needed Support site change controls, including impact assessments and quality reviews Provide technical review and guidance for investigations, documentation, and quality records Write, revise, and maintain QA procedures and controlled documents Support site quality metrics related to deviations, investigations, and complaint management Identify trends and support continuous improvement initiatives Promote a strong safety and quality culture through collaboration, mentorship, and technical coaching What You Need to Succeed (minimum qualifications): Education: Bachelor's degree in a scientific discipline preferred Experience: 6 years of Quality Assurance experience within a regulated industry (FDA, USDA, ISO, etc.) Top 2 Skills: Strong investigation and root cause analysis expertise combined with the ability to independently manage cross-functional quality initiatives in a GMP-regulated manufacturing environment. What Will Give You a Competitive Edge (preferred qualifications): 5+ years of experience with investigations, deviation management, and RCA tools (5 Whys, Ishikawa/6M, etc.) Experience reviewing and approving GMP documentation, investigations, and CAPAs Strong technical writing and communication skills Experience with risk assessment tools and quality metrics reporting Experience with electronic Quality Management Systems (eQMS) Demonstrated proficiency in Microsoft Office applications (Word, Excel, PowerPoint) Ability to manage multiple priorities with strong organizational skills Experience working collaboratively across manufacturing and quality functions Strong coaching and mentorship capabilities Experience within animal health or pharmaceutical manufacturing environments Additional Information: Travel: Occasional
Location: Elwood, KS The Elwood manufacturing facility is a 24/7/365 operation. This role primarily supports standard business hours but may occasionally require off-hour support to meet operational or compliance needs. Don't meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles! Elanco Benefits and Perks: We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include: Multiple relocation packages 8-week parental leave 9 Employee Resource Groups Annual bonus offering Flexible work arrangements Up to 6% 401K matching Elanco 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
  • United States

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  • English
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