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Charles River Laboratories

Technician - Clinical Laboratories

Montreal, QC, Canada

Salary: 23.75 $/per hour; · Full-time

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Job details

Pay: Salary: 23.75 $/per hour;
Job type: Full-time
Apply by: Dec 14, 2026
Posting language: English
Posted: Nov 14, 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

Technician – Clinical Laboratories

As a Technician for our Clinical Laboratories team at the Senneville location, you will perform technical activities and follows directives from the study/phase plan and the SOP.

In This Role, Primary Responsibilities Include

Perform the preparation and the analysis of samples;
Perform the quality control procedure and maintenances on the different instruments;
Perform the activities in a timely fashion by adhering to preset schedules;
Ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the GLP, SOP and health and safety rules.

If you have the following qualifications, we'll train you for the rest:

College diploma in science;
Relevant experience is an asset;
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above;
Readng and writing English is required. Bilingualism is preferred;
Ability to work under time constraint and adapt to change;
Demonstrate flexibility and ability to work independently.

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;
Salary: 23.75 $/per hour;
Schedule: Day shift 08h30 to 16h45
- Sunday to Thursday (off on Friday and Saturday) OR
- Tuesday to Saturday (off on Sunday and Monday);
Annual bonus based on performance;
Full time, permanent position (37.5 hours/week), depending on the needs, you may have to do overtime. Week-end prime (2.75$/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.

237246

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More about this job

Responsibilities

Prepare and analyze samples, perform quality control procedures, and maintain laboratory instruments according to study plans and standard operating procedures. Complete work on schedule while ensuring study integrity and compliance with Good Laboratory Practice, regulatory requirements, and health and safety rules.

Requirements

A college diploma in science is required, and relevant experience is an asset; an equivalent combination of education and experience may be accepted. Candidates must be able to read and write English and demonstrate adaptability, flexibility, and the ability to work independently under time constraints; bilingualism is preferred.

Skills

Sample Preparation
Sample Analysis
Quality Control
Instrument Maintenance
Good Laboratory Practice
Standard Operating Procedures
Regulatory Compliance
Health and Safety
Time Management
Adaptability
Flexibility
Independent Work
English Reading and Writing

Benefits

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

Visa sponsorship

Not detected in the job text

Keywords

Clinical Laboratories
Sample Preparation
Sample Analysis
Quality Control
Instrument Maintenance
Study Plans
Standard Operating Procedures
Good Laboratory Practice
Regulatory Compliance
Health and Safety
Laboratory Testing
Safety Assessment
Preclinical Drug Development
Biotechnology Research

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