Report Writer I, Medical Device Pathology

Role: Report Writer within Inotiv's medical device pathology team, responsible for preparing and quality-controlling pathology reports, data spreadsheets, and supporting study tracking to ensure accuracy and timely completion. Responsibilities include assisting pathologists, organizing study data, supporting audits, and maintaining documentation according to SOPs and GLP requirements. The role may involve cross-training in necropsy and histology support and performing administrative tasks related to study management. Requirements: Bachelor’s degree in a science-related discipline, proficiency in MS Office and Adobe Acrobat, familiarity with scientific report writing, and experience in regulated environments (FDA/GLP) preferred. Critical skills include strong organization, attention to detail, analytical/problem-solving abilities, and effective communication. High-value specifics: focus on GLP-regulated laboratory studies, supporting pathology data review and report generation, with an emphasis on quality assurance. Work environment: primarily in an office setting with some remote work possible, involving exposure to laboratory hazards and safety protocols. Physical demands include light activity, manual dexterity, and PPE use. The position offers multiple levels based on experience, with a salary range of $56,000–$65,000, aligned to qualifications, plus benefits.