Genetic Toxicology Analyst
1 month ago
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
Job Summary
As an Analyst for our Genetic Toxicology team located in Senneville, you will mainly conduct studies that evaluate the genotoxic and mutagenic potential of drugs at the early stages of drug discovery.
In this role, responsibilities may include:
- Perform the following techniques:
- Bacterial Mutation Test (BMT)
- Chromosome Aberration Test (CAT)
- InVitro Micronucleus (IVM)
- Mammalian Cell Mutation Test (MCM)
- Micronucleus Test (MNT), Comet Assay
- Cytotoxicity Test and Mode of Action Assay (MOA)
- Analysis of bacterial or cell cultures; manipulation of animal organs
- GLP-compliant collection and processing of analytical data
- Documentation of activities and data processing
- Work in collaboration with scientific staff
We are looking for the following minimum qualifications for this role:
- Collegial diploma in sciences or in related field
- Experience in the analysis of biological samples
- Flexible and able to adapt quickly to change
- Be meticulous, autonomous, reliable and possess good organizational skills
- Ability to work as part of a team
Role Specific Information:
- Location: Senneville / Free parking / Shuttle service from Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site
- Salary: 23$/hrs
- Annual bonus based on performance
- Schedule: weekday schedule, Monday to Friday
- Permanent position upon hiring, full time at 37.5hrs per week
Why Charles River?
- Competitive benefits upon hire. We pay up to 90% of premiums (medical & dental coverage)
- Paid development training
- Employee and family assistance program
- 24/7 access to a doctor and various health care professionals (telemedicine)
- 3 weeks’ Vacation & 5 Personal day policy
- Numerous organized social activities
If you want to contribute to the well-being of our communities, not only across the country, but around the world, join the team. This is Your Moment.
About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.
About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit www.criver.com.
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