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Technical Services & Manufacturing Science (TSMS) Scientist – Nights – 1023638 Elanco

Job in Topeka, Shawnee County, Kansas, 66652, USA
Listing for: Farmer Veteran Coalition
Full Time position
Listed on 2026-08-07
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Engineering
Salary/Wage Range or Industry Benchmark: 95000 - 130000 USD Yearly USD 95000.00 130000.00 YEAR
Job Description & How to Apply Below

About 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:

The Technical Services & Manufacturing Science (TSMS) Scientist is responsible for providing primary and/or secondary loop technical support for commercial operations at the Elwood, Kansas monoclonal antibody (mAb) manufacturing facility. This role serves as a subject matter expert for mAb products and processes and is actively engaged in tech transfer, scale-up, process optimization, validation, monitoring, troubleshooting, and continuous improvement initiatives. The TS/MS Scientist plays a critical role in supporting day-to-day operations and delivering technical projects.

Your

Responsibilities:
  • Provide technical and on-floor support for the commercialization, manufacture, and lifecycle management of monoclonal antibody products.
  • Collaborate with R&D, Manufacturing, and Quality teams to execute technical studies, validation activities, and technology transfer programs.
  • Support manufacturing teams with real-time troubleshooting and participate in investigations, including root cause analysis of deviations, complaints, and OOS/OOE events. Ensure proper documentation, CAPA development, and resolution within quality systems.
  • Act as a subject matter expert for product and process within cross-functional teams, projects, and governance forums.
  • Utilize scientific and statistical tools to improve process understanding, maintain process control, and identify opportunities for optimization and continuous improvement.
  • Lead and execute projects to address process performance issues and drive measurable improvements.
  • Support resolution of technical and compliance-related issues, including preparing technical assessments and responses for internal audits and regulatory agencies.
What You Need to Succeed (minimum qualifications):
  • Education:

    Bachelor's degree (or equivalent experience) in Bio/Pharmaceutical Technology, Microbiology, Engineering, or a related discipline.
  • Experience:

    Working knowledge of biopharmaceutical production processes and technologies, along with experience in a cGMP-regulated environment.
  • Top 2

    Skills:

    Strong analytical and problem-solving capabilities; and the ability to provide technical troubleshooting and collaborate effectively across cross-functional teams.
What will give you a competitive edge (preferred qualifications):
  • Advanced degree (MSc or PhD) in a related discipline.
  • 3+ years of experience in the biotech or pharmaceutical industry.
  • Experience with monoclonal antibody or recombinant protein manufacturing processes.
  • Experience in tech transfer, scale-up, and validation of biopharmaceutical processes.
  • Familiarity with SAP, JMP, and Veeva Vault systems.
  • Strong technical writing skills and experience applying tools such as RCI, FMEA, and QRM.
  • Working knowledge of USDA and/or EU GMP regulations for veterinary biologics.
Additional Information:
  • Location:

    Elwood, Kansas
  • Shift: Night shift position with weekend and evening rotation to support ongoing operations
  • Travel:
    Minimal (Don't meet every single requirement?Studies have shown under recognized 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 this role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate…
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