Genetic Toxicology Senior Scientist
- Baie-D'Urfé, QC
- Permanent
- Full-time
- Supervise laboratory staff and communicate with departmental management to ensure the smooth running of projects.
- Design assays, study plans, amendments and study schedules.
- Supervise the analysis of test items and samples in a multidisciplinary laboratory while respecting the Good Laboratory Practices (GLP / GLP).
- Analyze, correct and revise data.
- Write and review protocols and reports.
- Understand the purpose of each project under his/her responsibility and put strategies in place to achieve the defined objectives.
- Communicate with customers from the pharmaceutical industry.
- Comply with protocols, study plans, departmental and company’s SOPs.
- Minimum of Masters in Biology, Biotechnology, Biochemistry or other related discipline.
- Demonstrated 5 years’ industry experience working in the field.
- Hands-on experience with in vitro and in vivo genotoxicity essays, such as bacterial reverse mutation test (AMES), mammalian chromosome aberration test (MCAT) and rodent micronucleus test is required.
- Hands-on experience with in-vitro toxicology studies, such as skin irritation/corrosion, eye irritation, skin sensitization, phototoxicity, cytotoxicity tests, etc is an asset.
- Ability to run experiments in an autonomous manner. Good problem solving and analytical skills.
- Ability to work under time constraints and to adapt to change. Flexibility to work on changing work schedules.
- Good organizational skills. Knowledge and experience in Good Laboratory Practices (GLP) is required.
- Good Verbal and written communication skills in English and French.
- Detail oriented and meticulous. Ability to work well in a team environment.
- Permanent full-time job, 37.5 hours / week;
- Group insurance plan and group RRSP.
- A stimulating and friendly work environment.