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Added 48 mins ago
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Charles River Laboratories

Analyst I - Immunochemistry

Montreal, QC, Canada

Pay: Salary: 23.75$/hr;
Job type: Full-time
Apply by: Oct 24, 2026
Posting language: English
Posted: Sep 24, 2026

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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 Immunochemistry team located at the Ville St-Laurent site, you will participate in the analysis of serum, plasma, and tissue samples to verify the concentration, toxicity, and stability of assay substances (large molecules) in order to determine the safety and efficacy of drugs.

In This Role, Primary Responsibilities Include

Perform sample analysis work using various assays and techniques such as ELISA, Electrochemiluminescence (ECL), hybridization, and extractions;
Check the availability and prepare all required components related to its laboratory activities (literature, samples, solutions, material, equipment, etc.);
Compile appropriate data and present them properly, clear, readable and complete;
Perform data analysis to determine if results are within expectations;
Execute the technical activities described in the procedures and study plans while respecting the 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: 7170 rue Frederick-Banting, Saint-Laurent, QC, H4S 2A1;
Transportation: Free parking;
Salary: 23.75$/hr;
Annual bonus based on performance;
Schedule: Monday to Friday, 8am to 4:15pm. Depending on the needs, you may have to do overtime;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River?

We offer competitive benefits and advantages from day one to support your well-being;
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 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 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.

235966

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More about this job

Responsibilities

Analyze serum, plasma, and tissue samples using assays such as ELISA, electrochemiluminescence, hybridization, and extraction to assess drug-substance concentration, toxicity, and stability. Prepare laboratory materials, compile and analyze data, and carry out study procedures in accordance with Good Laboratory Practices.

Requirements

Requires a DEC in a science field such as biotechnology or medical laboratory science, or a bachelor's degree in immunology, biology, biochemistry, or an equivalent science discipline. Candidates should be organized, adaptable, autonomous, meticulous, detail-oriented, and able to work under time constraints.

Skills

Immunochemistry
ELISA
Electrochemiluminescence
Hybridization
Sample Extraction
Sample Analysis
Data Analysis
Good Laboratory Practices
Laboratory Procedures
Study Plan Execution
Data Compilation
Organization
Attention To Detail
Adaptability
Autonomy

Benefits

Performance Bonus
Employee And Family Assistance Program
Telemedicine
Three Weeks Of Vacation
Five Personal Days
Career Development Opportunities
Free Parking
Social Activities

Visa sponsorship

Not detected in the job text

Keywords

Immunochemistry
Serum Samples
Plasma Samples
Tissue Samples
ELISA
Electrochemiluminescence
Hybridization
Sample Extraction
Assay Analysis
Drug Concentration
Toxicity Assessment
Stability Assessment
Good Laboratory Practices
Laboratory Procedures
Study Plans
Data Compilation
Data Analysis
Biotechnology
Medical Laboratory Science
Immunology
Biology
Biochemistry
Preclinical Drug Development
Safety Assessment
Pharmaceutical Research

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