Inotiv

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.