Scientist - Biologics Analytical Development

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

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