Scientist - Biologics Analytical Development

- Zoetis India Capability Center; Oklahoma; On-site; USD 85,000 - 120,000; Full time

Job summary

Zoetis Veterinary Medicine Research and Development in Lincoln, NE is seeking an analytical assay scientist to execute ELISA/MSD methods, perform transfers, and support development across the lifecycle. The role emphasizes data analysis, documentation, and cross-functional collaboration.

The candidate should have BS/MS in life sciences with 5–7+ years of relevant industry experience, including biopharmaceutical or vaccine exposure.

Qualifications

• BS with 7+ years of experience in microbiology, biochemistry, biology or related field.
• MS with 5+ years of experience in the same disciplines.
• Minimum of 2 years in biopharmaceutical or vaccine industry.

Responsibilities

• Execute labs work for method development, qualification, validation, and transfer.
• Support ELISA/MSD and microbial assays; assist PCR/qPCR and cell-based assays.
• Trend method performance; investigate atypical results and root causes.
• Document procedures, results, and conclusions in ELNs and reports.
• Present data at project team meetings and in cross-functional discussions.
• Collaborate across process development and manufacturing teams.
• Apply basic statistics for DOE and experimental design.
• Maintain records and ensure safety and timely project completion.

Skills

ELISA/MSD assay execution

Data analysis

Design of experiments (DOE)

Statistical analysis

Documentation & reporting

Verbal and written English

Education

BS in microbiology/biochemistry/biology

MS in microbiology/biochemistry/biology

Job description

Zoetis Veterinary Medicine Research and Development, Biologics Analytical Sciences, located in Lincoln, Nebraska, is seeking an analytical assay scientist at the Scientist level.

This position is ideal for a highly motivated scientist who can execute analytical work, apply sound scientific judgment, and collaborate effectively within analytical teams to advance research and development programs. The successful candidate will primarily support routine testing using quantitative ELISA and MSD methods, as well as the optimization, qualification, validation, and transfer of these methods for biopharmaceutical products. The role will also support projects across the development lifecycle, from early to late-stage development and transfer into Quality Control.

Position Responsibilities

Responsibilities include, but are not limited to:

• Execute laboratory experiments in support of analytical method development, qualification, validation, transfer, and product characterization. Primary techniques may include quantitative ELISA/MSD and microbial assays, with opportunities to support additional methods such as PCR, qPCR and cell-based assays.
• Monitor, trend, and communicate method performance and critical reagent data; investigate atypical results and contribute to identification of potential root causes.
• Document experimental procedures, results, conclusions, and recommendations in electronic laboratory notebooks, technical reports, presentations, and other project documentation.
• Present analytical data and scientific conclusions at project team meetings and contribute to cross-functional discussions and decision-making.
• Collaborate with scientists and technical partners across process development and manufacturing.
• Apply basic statistical concepts and tools relevant to process control, method development, data analysis, and experimental design.
• Support laboratory operations by maintaining appropriate records, following applicable procedures and safety requirements, and helping ensure the timely completion of project activities.

Education & Experience:

BS with 7+ years of experience/MS 5+ years of experience in microbiology, biochemistry, biology or other related discipline.

Minimum of 2 years industry experience preferably in the biopharmaceutical or vaccine industry.

Technical Skills Requirements:

• Experience with quantitative ELISA/MSD assay execution, data analysis, troubleshooting, and method optimization.
• Excellent organizational and communication abilities (verbal and written English) with demonstrated skill in documentation, scientific writing (protocols, reports, journal articles) and presenting data and study summaries to project teams.
• Knowledge and experience in statistical analysis of assays, design of experiments (DOE), technical problem solving and continuous improvement is a plus.
• Experience with biopharmaceutical development and product licensure is a plus.
• Knowledge of the regulatory requirements (FDA, EMA, USDA) that apply to the development of tests for products tested under GMP release is a plus.

Full time

Regular

Colleague

Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at z