Technical Services & Manufacturing Science (TSMS) Scientist - Nights

Elanco•Elwood, KS

1d•Onsite

About The Position

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.

Requirements

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.

Nice To Haves

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.

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.