Veterinary Pathologist (Senior Principal Scientist)
Location: Kalamazoo, MI
Department: Veterinary Pathology - Clinical Pharmacology & Safety Sciences
Zoetis Veterinary Medicine Research and Development is seeking a driven and detail-oriented Veterinary Pathologist to join our Clinical Pharmacology and Safety Sciences team in Kalamazoo, MI. This is a high-impact role within a fast-paced, collaborative environment where your expertise will directly influence the development of safe and effective animal health products.
We are looking for an anatomic pathologist with extensive knowledge of anatomy, physiology, and pathology of common veterinary species, strong communication skills, and a passion for translational research - someone who will drive in vivo model development and provide pathology insights that shape discovery and development across multiple species (canine, feline, equine, bovine, small ruminants, swine, poultry, and commercial fish) and therapeutic areas (i.e. small molecule, biopharmaceuticals, and biologicals such as vaccines).
Key Responsibilities
Pathology Leadership & Study Oversight: Serve as the Project Pathologist for assigned compounds and therapeutic areas, leading pathology efforts for both internal and outsourced studies. Responsibilities include conducting gross necropsy and histopathology evaluations, integrating clinical pathology, organ weights, providing peer review to ensure consistency and scientific rigor, and guiding study design, data interpretation, and regulatory strategy.
In Vivo Study Design & Data Integration: Collaborate closely with toxicologists, target animal safety scientists, pharmacokineticists, and research scientists to design and interpret in vivo studies. Findings will support risk assessments and guide go/no-go decisions for candidate compounds.
GLP Compliance & Reporting: Act as a GLP Principal Investigator or contributing scientist for pathology, overseeing necropsy procedures, recording findings using electronic data capture pathology systems (e.g., Pristima), and preparing detailed reports that clearly communicate pathological outcomes. Work closely with study directors to ensure pathology data is accurately reflected in final study reports.
Pharmacovigilance Case Assessment: Contribute expert pathology evaluations to pharmacovigilance activities by assessing cases for safety signals and adverse event investigations, supporting the ongoing monitoring of marketed products to ensure animal health and welfare.
Cross-Functional Collaboration: Partner with target animal safety scientists, toxicologists, study directors, external study monitors, and project teams to interpret and communicate pathology findings clearly. Provide expertise to support the integration of pathology data into regulatory submissions, safety narratives, and responses to agency queries. Facilitate collaboration among internal and external stakeholders to ensure consistent and accurate interpretation of pathology results.
Innovative Research & Translational Science: Apply comparative pathobiology to support target validation, animal model development, and non-animal alternatives. Contribute to mode-of-action studies and experimental design, bridging preclinical findings with clinical relevance to improve candidate quality.
Regulatory Strategy & Documentation: Author regulatory submissions and address regulatory queries, ensuring pathology data is accurately and clearly represented in all regulatory documentation. Support compliance with GLP standards and regulatory approval processes.
Communication & Scientific Influence: Present pathology findings to project teams, senior leadership, scientific meetings and regulatory agencies, translating complex data into clear, actionable insights. Influence project strategy and play a critical role in advancing compounds through the development pipeline.
Mentorship and Oversight: Provide guidance and oversight to veterinary pathology interns, fostering their professional development and ensuring high standards of scientific... For full info follow application link.
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 [email protected] to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. 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. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at www.Zoetis.com/careers site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.
