Inotiv
Scientist, Genetic Toxicology
Rockville, MD
Sponsorship not specified$80k-$106kDetected 30 days ago
FDA RegulatoryResearchExperimental DesignCommunicationPublic SpeakingOrganizational Skills
About the role
- The salary range will adjust along with the level of the role to match the person's relevant experience and/or education level.
- 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.
Responsibilities
- Maintains overall scientific responsibility for the study design, interpretation, and reporting of study results
- 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
- Ability to make and document scientific observations
Requirements
- 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
- May develop and review new procedures, technologies, and SOPs as required
- If you have the talent and desire to impact the quality of people's lives, we have the career opportunities to make it happen.
- Ph.D. in a scientific discipline (i.e. Biology, Biochemistry, etc.)
Nice to have
- 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
Compensation
- 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.
- The salary range will adjust along with the level of the role to match the person's relevant experience and/or education level.
- Salary will be commensurate with experience and responsibilities.
Benefits
- include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more!
- This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.
- Attend continuing education courses, scientific conferences, or webinars, as appropriate
- Adherence to laboratory health and safety procedures.
- This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience.
- Join us in embracing research and science to impact the health and well-being of people all over the world.
Company info
- Inotiv is a growing contemporary drug discovery and development company where we "Play to Win" in an industry rich with opportunity.
Equal opportunity
- Equal Opportunity Employer.
This listing is sourced directly from Inotiv's careers page and normalized into a canonical job model.