Quality Assurance Associate - Manufacturing Floor (Day Shift)

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.

We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.

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 (...