Manufacturing Analytical Scientist

Apply to this position

Job Title: Manufacturing Analytical Scientist
Location: Elwood, KS, Midwest United States, USA

Company: Elanco
Industry Sector: Agribusiness
Industry Type: Input Retail, Cooperative and Related Crop Services
Career Type: Manufacturing/Production
Job Type: Full Time

Job 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. We're driven by our vision of 'Food and Companionship Enriching Life' and our approach to sustainability - the Elanco Healthy Purpose™ - to advance the health of animals, people, the planet and our enterprise.

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: Manufacturing Analytical Scientist

The Manufacturing Analytical Scientist is responsible supporting in-transfer, troubleshooting, optimization, and execution of analytical methods in support of product development activities at the Elwood, Kansas monoclonal antibody (mAb) manufacturing facility. The position is a subject matter expert with respect to analytical methods to analyze samples produced during mAb production and for final product testing. The subject matter expert acts as critical link between MSAT, QC and R&D.

Your Responsibilities:

Support in-transfer and optimization of new analytical methods for new product development, process improvement, and lifecycle management projects. Perform technical support and testing as required to support development / technical studies, method validations, and / or commercial product release.
Author and provide critical review of technical documents including but not limited to; development / technical study plans, SOPs, risk assessments, investigations, change controls, method validations, and stability protocols and reports. Define and coordinate sampling strategies, sample collection, handling, and testing requirements.
Collect and analyze method data, preparing and delivering presentation of results in technical forums & evaluate and implement new technologies (equipment, reagents, methods, etc) where appropriate to improve business outcomes.
Lead and participate in method-related investigations and root-cause analyses of OOS/OOE events. Ensure issues are identified and captured in the relevant quality management system and that proper root cause analysis is performed with appropriate corrective and preventative actions assigned.
Demonstrate strict adherence to relevant local, state and federal requirements, cGMP standards and Elanco policies and procedures. Exemplify "Safety First and Quality Always" mind-set.

What You Need to Succeed (minimum qualifications):

Education : Bachelor's degree in Chemistry , Bio/Pharmaceutical Technology, Microbiology, or a related discipline.
Experience : 5+ years' experience working in a laboratory / quality control setting.
Detailed understanding of analytical characterization methods for biological products, working knowledge of cGMP standards and experience working in a regulated environment, and demonstrated success operating in cross-functional teams.
Experience with at least one of the following: HPLC, UPLC, ELISA, SoloVPE, CE-SDS.

What will give you a competitive edge (preferred qualifications):

MSc or PhD in Chemistry, Bio/Pharmaceutical Technology, Microbiology, or a related discipline.
Experience in tech transfer, optimization, and validation of analytical methods for characterization of biological products (eg. mAbs, recombinant proteins, vaccines).
Demonstrated success leading cross-functional teams / projects.
Experience with SAP, JMP, Veeva Vault.
Excellent technical writing skills.
Working knowledge of VICH, USDA and/or EU GMP regulations for veterinary biologics.

Additional Information:

Travel: Minimal travel requirements

Location: Elwood, Kansas
Day shift position. Weekend and evening work not usual, although may be required to provide process support to ongoing operations.

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

To apply please click on APPLY TO THIS POSITION

Job Post Date: 05/09/25