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Sr. Associate, Quality Assurance Validation

External
elanco logoElanco · Elwood, KS
Full-timeOn-siteToday
ComplianceDocumentationExcelLessSAP
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Responsibilities

  • Support and oversee computer system validation (CSV) activities and contribute to maintaining and improving data integrity processes across the site. Drive continuous improvement and standardization of equipment and system lifecycle documentation aligned with Elanco operational standards.
  • Ensure compliance with cGMP and regulatory requirements by performing Quality review and oversight of site documentation. Support internal audits and regulatory inspections as needed, and promote a "Safety First and Quality Always" culture across all activities.
  • What You Need to Succeed (minimum qualifications):
  • Education: Bachelor's degree in a science or engineering discipline.
  • Experience: 5+ years of experience in quality, engineering, or validation roles within the biologics or pharmaceutical industry. Experience in equipment lifecycle management and computer system validation (CSV).
  • Top 2 Skills: Strong organizational and communication skills with high attention to detail; ability to collaborate effectively across cross-functional teams and multiple organizational levels. Proficiency with Microsoft Office (Word, Excel, PowerPoint, Outlook).
  • What will give you a competitive edge (preferred qualifications):
  • Experience in materials management within USDA, FDA, or EMA regulated environments. Demonstrated success leading cross-functional teams or projects. Experience with SAP, JMP, and Veeva Vault systems. Working knowledge of VICH, USDA, and/or EU GMP regulations for veterinary biologics.
  • Additional Information:
  • Location: Elwood, Kansas (Onsite).
  • Day shift position. Weekend or evening work may occasionally be required to support operations.
  • Minimal travel required ( Full-time, permanent, salaried position.
  • Don't meet every single requirement?
  • 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 for eligible roles
  • 8-week parental leave
  • 9 Employee Resource Groups
  • Annual bonus offering
  • 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 le

Benefits

Health insuranceVision insurance401(k)Performance bonusParental leave

Additional Information

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: Sr. Associate, Quality Assurance Validation The Sr. Associate, Quality Assurance Validation serves as a key Quality representative supporting capital projects, commissioning, qualification, and computer system validation (CSV) activities at the Elwood, Kansas monoclonal antibody (mAb) manufacturing facility. This role partners closely with engineering, validation, and cross-functional teams to ensure facilities, utilities, equipment, and systems are designed, qualified, and maintained in compliance with regulatory requirements. The position plays a critical role in ensuring data integrity, regulatory readiness, and adherence to cGMP standards while supporting the full lifecycle of capital and validation projects.


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