Scientist, Genetic Toxicology

Scientist, Genetic Toxicology Qualifications Ph.D. in a scientific discipline (i.e. Biology, Biochemistry, etc.) Master’s degree in a scientific discipline (i.e. Biology, Biochemistry, etc.) with 2+ years of relevant work experience Bachelor’s degree in a scientific discipline (i.e. Biology, Biochemistry, etc.) with 4+ years of relevant work experience Preferred Qualifications Working knowledge of a research or testing laboratory Laboratory experience in conducting GLP‑regulated studies Possess good interpersonal and strong written and verbal communication skills Highly motivated and detail oriented with good organizational skills Possess the ability to multitask and work independently or in a team environment with minimum supervision Experience working in a regulated environment Working knowledge and application of FDA and EPA regulations (GLP) and ICH guidelines Experience in Mammalian Mutation (CHO-HPRT and Mouse Lymphoma or Bacterial Mutation assays Good computer skills in word processing, spreadsheets, presentations and lab information systems, specifically MS Office., Corporate Responsibilities Adherence to laboratory health and safety procedures. Adherence to Standard Operating Procedures (SOPs). Adherence to applicable company policies and guidelines. Adherence to federal and/or local regulations, as applicable. Position Responsibilities Study Director must fulfill all aspects of the role, as outlined in the GLP regulations Maintains overall scientific responsibility for the study design, interpretation, and reporting of study results Interacts with Sponsors or clients to present and interpret results Serves as scientific resource in Genetic Toxicology and will generally serve as an endpoint expert in at least one area of genetic toxicology Reviews and recommends potential assay developments to upper management, and participates in initiatives and/or projects to drive improvement in quality and/or client service Manages studies in accordance with established protocols, SOPs, and pertinent regulatory requirements Reviews training of technical staff to ensure adequacy to perform study‑specific techniques May develop and review new procedures, technologies, and SOPs as required Ability to make and document scientific observations Other duties as assigned Professional Responsibilities Attend continuing education courses, scientific conferences, or webinars, as appropriate The annual pay range estimated for this position is $80,100.00-$105,500.00. Please note that hourly rates/salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more! Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training. #J-18808-Ljbffr