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Quality Assurance Associate – Manufacturing Floor; Day Shift – Elanco

Job in Salina, Saline County, Kansas, 67401, USA
Listing for: Farmer Veteran Coalition
Full Time position
Listed on 2026-07-25
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers, Production QC/QA, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 65000 - 90000 USD Yearly USD 65000.00 90000.00 YEAR
Job Description & How to Apply Below
Position: Quality Assurance Associate – Manufacturing Floor (Day Shift) – 1016059 Elanco

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 – Manufacturing Floor

This position coordinates and conducts activities of the Quality Assurance Department regarding manufacturing floor support and has specific responsibilities for other quality and compliance related activities as directed by the Quality Assurance Manager. This position plays a key role in day-to-day operations and works very closely with the Manufacturing and Process Teams.

Your Responsibilities
  • Actively interact with Manufacturing and champion compliance through leadership and example in daily processes.
  • Provide quality floor support, including observing daily active processes for statuses, issues, concerns, and issuance of cell banks.
  • Act as first responder for manufacturing activities and represent QA on cross‑functional process teams.
  • Identify, investigate, and resolve complex technical issues using problem‑solving skills.
  • Participate in investigation teams, determine next steps and assist in the proper close out and follow up actions.
  • Make decisions independently and notify management of actions taken.
  • Perform QA review/approval of controlled documents including, but not limited to, solution records, batch records, logbooks, autoclave cycles with a high attention to detail, using extensive working knowledge of quality concepts and internal procedures and controls.
  • Review change management documentation, deviations, investigations and CAPA records for completion.
  • Write new documents and revise existing QA documents as needed.
  • Participate and manage QA projects as needed with minimal supervision. Receive overall project direction from management but complete most work independently.
  • Assist other Quality Assurance Associate(s) and Quality Assurance Manager(s) as needed.
What You Need to Succeed (Minimum Qualifications)
  • BA/BS (or Master's) in any Life Science discipline preferred, and/or 3 years' experience in regulated industry (USDA, FDA, ISO etc).
  • Must have direct experience with Quality Assurance within regulated industry (USDA, FDA, ISO, etc.)
  • Understands and applies comprehensive knowledge of quality and GMP principles and maintains current understanding of global GMP drug manufacturing regulations.
  • Must be able to work in controlled / clean room environments requiring gowning qualifications.
What Will Give You the Competitive Edge (Preferred Qualifications)
  • Familiarity with basic statistics, review/approval of documentation; risk tools, technical writing, and writing/reviewing/approving investigations.
  • Ability to handle multiple tasks and competing priorities concurrently and in a timely fashion.
  • Good interpersonal skills and ability to work effectively and efficiently in a team environment to accomplish goals.
  • Demonstrated experience making sound independent decisions.
Additional Information

Location:

Elwood, KS Manufacturing Site

Must be able to work in controlled / clean room environments requiring gowning qualifications.

Day Shift

Hours:

8am – 4:30pm, Monday – Friday. Rotating weekend schedule required (every 3rd weekend) 24/7 hr. site

Elanco Benefits and Perks:

  • Multiple relocation packages
  • 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 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 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.

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Position Requirements
10+ Years work experience
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