Technical Services & Manufacturing Science (TSMS) Scientist - Nights

Elanco; Elwood (KS); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Multiple relocation packages

8-week parental leave

Annual bonus offering

Up to 6% 401(k) matching

Job summary

Elanco is seeking a TS/MS Scientist for their Elwood, Kansas monoclonal antibody manufacturing facility. This position is crucial for providing technical support for commercial operations, including troubleshooting and process optimization.

The ideal candidate will possess a Bachelor’s degree in a relevant field and have experience in the biopharmaceutical industry. This role requires collaboration with R&D, Manufacturing, and Quality teams to ensure effective product lifecycle management.

Benefits include relocation packages, parental leave, and 401(k) matching.

Qualifications

• Working knowledge of biopharmaceutical production processes and technologies.
• Experience in a cGMP-regulated environment.
• Experience with monoclonal antibody or recombinant protein manufacturing processes.

Responsibilities

• Provide technical and on-floor support for commercialization and manufacture.
• Collaborate with R&D, Manufacturing, and Quality teams.
• Support manufacturing teams with real-time troubleshooting.

Skills

Analytical skills

Problem-solving

Technical troubleshooting

Collaboration

Education

Bachelor’s degree in Bio/Pharmaceutical Technology, Microbiology, Engineering, or related discipline

Tools

SAP

JMP

Veeva Vault

Job description

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.

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.
• Strong analytical and problem‑solving capabilities; and the ability to provide technical troubleshooting and collaborate effectively across cross‑functional teams.

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 with weekend and evening rotation to support ongoing operations
• Travel: Minimal

Benefits and Perks

• Multiple relocation packages
• 8‑week parental leave
• 9 Employee Resource Groups
• Annual bonus offering
• Up to 6% 401(k) matching

EEO Statement

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.

Recruitment Process

Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferable 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.