• Serves as the study pathologist for nonclinical studies conducted in compliance with applicable FDA and other national and international regulatory agency standards. • Performs pathology services, to include 1) development of protocol pathology methodologies, 2) interpretation of gross, microscopic and clinical pathology study data (if applicable), 3) consultation with clients and study directors on pathology findings, and 4) completion of timely and accurate protocol-driven pathology reports. • Collaborates with facility veterinarians as needed to generate diagnostic pathology data and interpretation of results in support of colony health objectives and needs. • Participates in necropsies as appropriate and may train Associates participating in necropsies. • Provides technical guidance to histologist on histological preparations. • Assists in training department personnel in gross pathology and histology procedures, with guidance based on client goals, organizational needs, and company policy. • Completes study reports and pathology assignments according to management study prioritization schedule. • Works in conjunction with the Quality and Scientific Affairs to develop and maintain study integrity and GLP compliant processes. • Represents NAMSA through seminars, client visits, and shows. This includes writing articles for publication or presentation. • Maintains a GLP-compliant workspace, performs calibration/validation activities as required, operates equipment and performs tasks in compliance with all applicable SOPs. • Assists in research to develop techniques for identifying and interpreting pathological conditions. • Maintains a GLP-compliant workspace, performs calibration/validation activities as required, operates equipment and performs tasks in compliance with all applicable SOPs.