Scientist - Biologics Analytical Development

6J6 - Zoetis LLC; Oklahoma; On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Competitive healthcare

Retirement savings benefits

Employee well-being programs

Job summary

Zoetis Veterinary Medicine Research and Development in Lincoln, NE seeks an analytical assay scientist to execute ELISA/MSD methods, support qualification/validation and technology transfer across development stages. You will collaborate with process development and manufacturing teams to advance biopharmaceutical programs.

The role involves data analysis, statistical thinking, and documentation in ELNs and reports, with opportunities to contribute to diverse assay platforms and regulatory

Qualifications

• BS/MS in microbiology/biochemistry with 7+ years (BS) or 5+ years (MS) in related discipline.
• Minimum of 2 years industry experience, preferably in biopharmaceutical or vaccine industry.
• Experience with quantitative ELISA/MSD assay execution, data analysis, troubleshooting, and method optimization.
• Knowledge of regulatory requirements (FDA, EMA, USDA) for GMP-released products is a plus.

Responsibilities

• Execute laboratory experiments supporting analytical method development, qualification, validation, transfer, and product characterization.
• Perform quantitative ELISA/MSD and microbial assays; support PCR/qPCR and cell-based assays as needed.
• Monitor method performance, investigate atypical results, and identify root causes.
• Document procedures and results in ELNs and reports; present data in project meetings.

Skills

ELISA

MSD

PCR/qPCR

Cell-based assays

Data analysis

DOE

Regulatory knowledge

Education

BS/MS in microbiology/biochemistry

Tools

ELISA instruments

qPCR machines

Statistical software

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

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

Company & Culture

At Zoetis, our purpose is to nurture our world and humankind by advancing care for animals. As a Fortune 500 company and the world leader in animal health, we discover, develop, manufacture and commercialize vaccines, medicines, diagnostics and other technologies for companion animals and livestock. We know our people drive our success. Our award-winning culture, built around our Core Beliefs, focuses on our colleagues’ careers, connection and support.

Equal Opportunity and Diversity

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.

Accommodation for Disabled Individuals

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.

Sponsorship & Work Authorization

All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact.

Benefits

• competitive healthcare and retirement savings benefits
• an array of benefits, policies and programs to support employee well-being in every sense, from health and financial wellness to family and lifestyle resources