Quality Assurance Associate - Supplier Management

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: Quality Assurance Associate - Supplier Management As a Quality Assurance Associate - Supplier Management, you will support quality and compliance activities at our Elwood, Kansas facility. In this role, you will be responsible for material and packaging release activities, specification management, audit support, quality system records, and cross-functional collaboration with Manufacturing, Warehouse, and Supply Chain teams to ensure compliance with regulatory and quality standards. Your Responsibilities: Manage quality assurance activities related to material movement, including disposition, hold, rejection, and release of incoming materials. Support Manufacturing and Warehouse teams by promoting compliance through leadership, collaboration, and day-to-day quality oversight. Own the lifecycle management of material and packaging specifications, including drafting, annual review, and revision updates. Conduct gap assessments for material, packaging, labeling specifications, and Standard Operating Procedures (SOPs). Draft, route, and complete quality system records including change controls, deviations, CAPAs, and investigations within the Veeva Quality Management System. Participate in and lead internal and supplier audits while supporting documentation requests for external regulatory audits. Analyze quality events, investigations, and projects to determine appropriate actions and independently resolve complex technical and compliance issues. Represent Quality Assurance on cross-functional project teams and provide quality guidance to support business objectives. Author and revise quality documents, procedures, and records to maintain compliance with applicable regulations and internal standards. Conduct SAP transactions to support material release activities and verify data accuracy within the system. Support records management and archival activities while assisting other Quality Assurance team members as needed. What You Need to Succeed (minimum qualifications): Education: Bachelor's degree in a Life Science discipline preferred, or equivalent combination of education and experience. Experience: Minimum of 5 years of experience in a regulated industry (USDA, FDA, ISO, GMP, or similar) with direct Quality Assurance experience. Strong understanding of quality systems, GMP principles, and applicable regulatory requirements. Experience reviewing and approving quality documentation, investigations, deviations, CAPAs, and change controls. Demonstrated ability to make sound independent decisions and manage multiple priorities simultaneously. Strong technical writing, analytical, and problem-solving skills. Excellent verbal and written communication skills. Proficiency with Microsoft Office applications including Word, Excel, and PowerPoint. Ability to work effectively in a collaborative team environment. What Will Give You a Competitive Edge (preferred qualifications): Bachelor's degree in Biology, Microbiology, Chemistry, Biochemistry, or another Life Science field. Experience with Veeva Quality Management Systems and SAP. Knowledge of risk management tools and basic statistical analysis. Experience conducting supplier, internal, and regulatory audits. Familiarity with USDA, FDA, ISO, and GMP requirements within pharmaceutical, biotechnology, or veterinary biologics manufacturing environments. Demonstrated project management experience and ability to lead quality initiatives across functional teams. Experience supporting continuous improvement and compliance-focused programs. Additional Information: Travel: 0–5% Location: Elwood, Kansas 24/7 Manufacturing Facility 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% 401(k) 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 Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.