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Added 12 mins ago
A
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Charles River Laboratories

Analyst I - Immunotoxicology

Montreal, QC, Canada

Salary: $23.75$/hr. · Full-time

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Job details

Pay: Salary: $23.75$/hr.
Job type: Full-time
Apply by: Nov 30, 2026
Posting language: English
Posted: Oct 31, 2026

Original job description

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 Overview

As an Analyst for our Immunotoxicology team located at the Senneville site, you will be involved in analyzing immune system dysfunctions that can result from occupational, inadvertent, or therapeutic exposure to a variety of chemical or biologic agents that alter the immune system and affect human health.

In This Role, Primary Responsibilities Include

Perform sample analysis work using various assays and techniques such as ELISA, ECL, Cell Culture, PBMC extraction, Luminex, ELISPOT, and Flow Cytometry;
You will also perform data analysis to determine if results are within expectations; all in accordance with Good Laboratory Practices (GLP).

We are looking for the following minimum qualifications for this role:

Holder of a DEC in Science (Biotechnology, Medical Laboratory, or equivalent) or a BAC in Science (Immunology, Biology, Biochemistry);
Ability to work under time constraints;
Outstanding organizational skills and ability to adapt to changes;
Autonomous, meticulous and detail oriented.

Role Specific Information

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a shuttle service from Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. In addition, the site is accessible from the Anse-à-l’Orme REM station via STM bus services. Free parking. Electric vehicle charging station;
Annual bonus based on performance;
Schedule: Monday to Friday, daytime;
Permanent position as of the hiring, full-time 37.5hrs per week;
Salary: $23.75$/hr.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. 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 is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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.

236746

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More about this job

Responsibilities

Perform immunotoxicology sample analyses using assays and techniques including ELISA, ECL, cell culture, PBMC extraction, Luminex, ELISPOT, and flow cytometry. Analyze results to determine whether they meet expectations and conduct all work in accordance with Good Laboratory Practices.

Requirements

Applicants must hold a DEC in a science field such as biotechnology or medical laboratory studies, or a bachelor's degree in a science field such as immunology, biology, or biochemistry. They should be able to work under time constraints and demonstrate strong organizational skills, adaptability, autonomy, meticulousness, and attention to detail.

Skills

ELISA
Electrochemiluminescence (ECL)
Cell Culture
PBMC Extraction
Luminex
ELISPOT
Flow Cytometry
Data Analysis
Good Laboratory Practices (GLP)
Organization
Adaptability
Attention to Detail
Autonomy

Benefits

Performance-Based Annual Bonus
Free On-Site Gym
Employee and Family Assistance Program
Career Development Opportunities
Telemedicine and Access to Health Professionals
Three Weeks of Vacation
Five Personal Days
Social Activities
Free Parking
Electric Vehicle Charging Station
Shuttle Service

Visa sponsorship

Not detected in the job text

Keywords

Immunotoxicology
Immunology
ELISA
Electrochemiluminescence (ECL)
Cell Culture
PBMC Extraction
Luminex
ELISPOT
Flow Cytometry
Sample Analysis
Data Analysis
Good Laboratory Practices (GLP)
Biotechnology
Medical Laboratory
Biology
Biochemistry
Immune System Dysfunction
Chemical Agents
Biologic Agents
Safety Assessment
Preclinical Drug Development

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