Technical Services & Manufacturing Science (TSMS) Scientist
Elanco Animal Health Incorporated
·Jul 13, 2026
- Location
- Elwood, KS, United States of America
- Type
- Full-time
- Department
- IT
- Experience
- 3+ years
- Education
- Master
- Source
- Workday
Description
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: Technical Services & Manufacturing Science (TSMS) Scientist
The Technical Services & Manufacturing Science (TSMS) Scientist is responsible for providing operational and technical support for commercial and pilot laboratory operations at the Elwood, Kansas, monoclonal antibody (mAb) manufacturing facility. The position is a subject matter expert with respect to mAb products and processes and is engaged in tech transfer, scale-up, process optimization, validation, monitoring, troubleshooting, and continuous improvement activities.
Your Responsibilities:
Support the execution and troubleshooting of upstream and/or downstream manufacturing processes for biologics (e.g., mammalian cell culture, purification).
Collaborate with Manufacturing, Development, and Quality teams in the execution of technical / development studies, investigations, validation activities, and technical transfer programs, and collaborate with team members to identify potential risks, sources of variability, improvement, and value engineering opportunities to maximize project return and likelihood of technical success.
Provide on-floor support during manufacturing campaigns, including troubleshooting and deviation investigations.
Use scientific and statistical analysis tools to improve process understanding, ensure manufacturing processes are capable and operating in a state of control, and identify opportunities for process improvements.
Author and provide critical review of technical documents, including, but not limited to: batch records, SOPs, PFDs, risk assessments, investigations, technical studies, commissioning and qualification protocols, and reports.
Assist in implementing changes through the change control system (e.g., BOM updates, process changes).
What You Need to Succeed (minimum qualifications):
Education: Master's or Bachelor’s degree or equivalent in Bio/Pharmaceutical Technology, Microbiology, Engineering, or a related discipline.
Experience: 3+ years of experience in the Biotech / Pharmaceutical industry. Must have hands-on experience with chromatography (including Protein A or affinity chromatography), bioreactor operation, and tangential flow filtration (TFF).
Top Skills: Familiarity with data analysis tools such as JMP or Excel is preferred. Candidates should be able to work effectively in a team environment and support manufacturing activities on the production floor, including occasional off-shift or weekend coverage as needed. A strong understanding of biopharmaceutical production processes, along with working knowledge of cGMP standards and experience in regulated environments, is required.
What will give you a competitive edge (preferred qualifications):
Advanced degree (MSc) in Bio/Pharmaceutical Technology, Microbiology, Engineering, or a related field.
Hands-on experience in commercial manufacturing of monoclonal antibodies and/or recombinant proteins.
Proven track record in tech transfer, process scale-up, and validation within biopharmaceutical operations.
Experience with capital project execution and familiarity with electronic quality systems (e.g., Veeva QMS, TrackWise) and MES platforms.
Additional Information:
Location: Elwood, Kansas
Day shift position. Weekend and evening work is not usual, although it may be required to provide process support to ongoing operations.
Minimal travel requirements < 10%.
Don’t meet every single requirement? Studies have shown underrecognized 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
8-week parental leave
9 Employee Resource Groups
Annual bonus offering
Flexible work arrangements
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.
