Quality Assurance Assistant

ElancoClinton, IN
Onsite

About The Position

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 Assistant As a Quality Assurance Assistant, you will support site quality systems to ensure products and packaging meet all applicable cGMP standards and regulatory requirements. In this role, you’ll be responsible for reviewing and analyzing data, maintaining documentation, and partnering cross-functionally to enable timely batch release and production support.

Requirements

  • High School Diploma / GED Required
  • Experience in a manufacturing, quality, or regulated environment (cGMP preferred)
  • Attention to detail
  • Ability to manage multiple priorities in a fast-paced environment

Nice To Haves

  • Experience working in a cGMP-regulated manufacturing environment
  • Hands-on experience with batch record review, material release, or quality documentation
  • Familiarity with document management systems (e.g., Veeva Vault) and ERP systems such as SAP
  • Experience supporting quality activities for packaging, labeling, or certificates (COAs, permits, etc.)
  • Strong communication skills with ability to collaborate across Quality, Operations, and Supply Chain

Responsibilities

  • Review, organize, and maintain manufacturing records, ensuring accuracy, completeness, and compliance with GMP standards
  • Support quality systems, including document management, SOP creation/revision, and routing documents through systems such as Veeva Vault
  • Partner with Production, QC, and Supply Chain to ensure timely batch release and communication of critical quality information
  • Perform material-related quality activities including raw material approval, vendor COA review, and printed packaging inspection
  • Prepare and manage documentation such as Certificates of Analysis, labels, and batch records to support production and customer requirements

Benefits

  • Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)
  • 8-week parental leave
  • 9 Employee Resource Groups
  • Annual bonus offering
  • Up to 6% 401K matching

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Education Level

High school or GED

Number of Employees

1,001-5,000 employees

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