Technical Services & Manufacturing Science; TSMS Scientist

Your Role

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.

• 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 and development studies, investigations, validation activities, and technical transfer programs, and identify potential risks, sources of variability, improvement, and value engineering opportunities.
• 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 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).

• Education: Master’s or Bachelor’s degree or equivalent in Bio/Pharmaceutical Technology, Microbiology, Engineering, or a related discipline.
• Experience: 3+ years in the Biotech or Pharmaceutical industry with hands‑on experience in 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; ability to work effectively in a team environment and support manufacturing activities on the production floor, including occasional off‑shift or weekend coverage as needed.
• Strong understanding of biopharmaceutical production processes, cGMP standards, and experience in regulated environments.

• Advanced degree (MSc) in 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, Track Wise) and MES platforms.

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%.

• Multiple relocation packages
• 8‑week parental leave
• Employee Resource Groups
• Annual bonus
• Flexible work arrangements
• Up to 6% 401(k) 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 its recruitment process, but all hiring decisions involve a human reviewer.