More jobs:
Technical Services & Manufacturing Science; TSMS Scientist - Nights
Job in
Lenexa, Johnson County, Kansas, 66215, USA
Listed on 2026-06-06
Listing for:
Elanco Tiergesundheit AG
Full Time
position Listed on 2026-06-06
Job specializations:
-
Science
Biotechnology, Data Scientist
Job Description & How to Apply Below
Elwood, KStime type:
Full time posted on:
Posted Yesterday job requisition : R0025371
** 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, Nights
** 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 (
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