Analytical Scientist / Sr. Scientist

Zoetis•Lincoln, NE

2d•Onsite

About The Position

Zoetis is the world’s largest Manufacturer and Supplier of Animal Pharmaceuticals. At Zoetis in Lincoln, NE, we manufacture high quality medicines for dogs, cats, and livestock. Our plant has been recognized as one of the Nebraska’s Safest Companies, with a long-standing presence in the Lincoln community. We are a clean, modern site that continues to innovate and grow. Benefits Include: 4 weeks accrued paid vacation and 13 paid holidays. 401(k) match with company profit sharing. Tuition reimbursement and Student Loan repayment program. Great Health, personal, and family benefits starting day 1. Position Summary The Analytical Scientist / Sr Scientist performs analytical assays to qualify and/or requalify reference reagents, evaluate potency and clinical assays, and analyze reagents and formulation samples for various biological products that are released using reference reagents. Primary techniques include viral or bacteriological potency or clinical ELISA based assays, bacterial propagation and isolation, and tissue culture-based assays, including virus neutralization and virus isolation. Responsibilities include leading and contributing to Reference Qualification (RQ) projects to milestones and deliverables (e.g., qualifying serial preparations / testing and clinical sample evaluations), designing and conducting laboratory experiments to develop, validate and/or transfer analytical assays, preparing necessary documentation (e.g., reports, protocols, test methods, Outlines / Special Outlines and Standard Operating Procedures), and managing reagent and sample inventories. The position collaborates with cross-functional partners to achieve RQ objectives while maintaining compliance with applicable regulations and internal policies. Hours: 1st Shift.

Requirements

BSc or MSc in a relevant discipline (e.g., biochemistry, analytical chemistry, biotechnology, microbiology) or equivalent experience.
3+ years of relevant laboratory experience (e.g., ELISA, cell-based assays including virus neutralizations).
Strong technical/scientific writing skills.
Understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
Excellent interpersonal and communication skills.
Knowledge of analytical method development, transfer, and validation.
Familiarity with Center for Veterinary Biologics requirements (e.g., VSM 800.112, VSM 800.211).
Ability to manage multiple priorities in a fast-paced environment.
Critical thinking and problem-solving skills; high attention to detail and organization.
Proficiency in Microsoft Excel, Word, and PowerPoint, experience with SoftMax Pro and SAP is advantageous.

Responsibilities

Utilize expertise in analytical assays, especially ELISA, virus neutralization assays, bacterial propagation and isolation and cell cultures.
Lead and contribute to RQ projects, achieving milestones and deliverables (e.g., qualifying serial preparations / testing and clinical sample evaluations).
Independently design studies and prepare analytical protocols, methods, and reports.
Modify established procedures to improve efficiency, robustness, and quality.
Apply sound judgment and prior experience to troubleshoot, solve problems, and propose practical solutions.
Provide training, coaching, and mentorship within the RQ team.
Ensure compliance with regulatory requirements, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), health and safety requirements, and corporate policies.
Maintain accurate inventories of reagents and samples; ensure data integrity and traceability.