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Quality Assurance Associate, On the Floor (2nd shift 2:00PM-10:00PM)

Elanco
Posted 18 days ago, valid for 19 days
Location

Fort Dodge, IA, US

Salary

Competitive

Contract type

Full Time

Paid Time Off

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Sonic Summary

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  • Elanco is seeking a Quality Assurance Associate for the 2nd shift (4PM-2:30AM) to support process teams in continuous improvement and compliance auditing.
  • Candidates must have an Associate's Degree in a science-related field and relevant industry experience, or a Bachelor's Degree in a related field, along with previous experience in a biological production environment with USDA/FDA regulations.
  • The role involves reviewing product batch records, tracking improvement goals, and training personnel on GMP/GDP standards.
  • Elanco offers a comprehensive benefits package including multiple relocation options, 8-week parental leave, and up to 6% 401K matching.
  • Salary details are not explicitly mentioned, but the position encourages diverse applicants to apply even if they don't meet every requirement.

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, On the Floor (OTF)

 

Shift: (2nd shift 2PM-10:00PM)

 

This position supports the Process Teams by tracking/reporting/and defining continuous improvement goals, on-the-floor batch record review/determining root cause for deviations/investigation report writing, coaching/training personnel on GMP/GDP, auditing production processes for compliance to global and local procedures, and closely working with and reporting to the Process Team Lead and Quality Lead.

 

Your Responsibilities:

  • Review and approve product batch records and technical documentation associated with validation, deviations or change control activities (media fills, etc.).

  • Track/report/and define continuous improvement goals, determine root cause for deviation/CAPA reports, and subsequent communication back to the Process Team.

  • Audit production processes for compliance with global and local procedures and either create new or revise existing procedures as changes occur.

  • Develops training plans and trains/qualifies others, including training outside of area of responsibility.

  • Demonstrates understanding of regulations for various countries and provides input or approval accordingly.

 

What You Need to Succeed (Minimum Requirements):

  • Associate's Degree in a science-related field and relevant industry experience or a Bachelor's Degree in a science-related field (Biology, Chemistry, etc.). 

  • Previous experience with USDA/FDA regulatory requirements in a biological production environment. 

  • Previous experience utilizing computer programs such as Microsoft suite, SAP, Veeva, Learning One Source and other relevant electronic applications.

 

What Will Give You a Competitive Edge (Preferences):

  • Ability to make decisions with minimal supervision regarding the acceptability of product based on documentation provided.

  • Excellent attention to detail.

  • Continuously demonstrates a high level of professionalism through interactions with internal and external customers.

  • Must be capable of formulating new ideas for improving site performance and efficiency and working cohesively with all levels to implement ideas.

 

Don’t meet every single requirement? Studies have shown underrepresented 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 for eligible positions

  • 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 

 

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.




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