Job Title:

Scientist, Genetic Toxicology

Qualifications:

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

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.

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*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. 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!