Scientist, Genetic Toxicology

Inotiv•Rockville, MD

1d•Onsite

About The Position

Inotiv is a growing contemporary drug discovery and development company where we “Play to Win” in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There’s an opportunity for everyone at all phases of a career, each individual’s unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people’s lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world.

Requirements

Ph.D. in a scientific discipline (i.e. Biology, Biochemistry, etc.) – OR – Master’s degree in a scientific discipline (i.e. Biology, Biochemistry, etc.) with 2+ years of relevant work experience – OR – Bachelor’s degree in a scientific discipline (i.e. Biology, Biochemistry, etc.) with 4+ years of relevant work experience
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.

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.
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
Attend continuing education courses, scientific conferences, or webinars, as appropriate