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Added 37 mins ago
CK
Senior Financial Analyst, Financial Information and Controls
Circle K
Laval, QC
- Full-time
…with senior management and for external purposes to meet the regulatory requirements of a public…
Added 7 hours ago
TC
Home Share Coordinator (Quality Analyst), Full-Time
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Langley (District), BC · Langley, BC
- Full-time
The Home Share Coordinator (Quality Analyst - QA) oversees home share providers who, under an agreement with Taproot, share their home with a person(s) with a developmental disability. The…
Added 8 hours ago
CR
Scientist in Immunochemistry
Charles River Laboratories
Montreal, QC
- Full-time
…facility, you will be responsible for the design, conduct and reporting of Laboratory Sciences studies efficiently, profitably and with the maximum scientific quality. Your success will…
Added 9 hours ago
KR
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- Full-time
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Added 11 hours ago
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- Full-time
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- Contract
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Analyste De Finance
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- $48 to $56 CAD / hour
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Added 11 hours ago
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Analyst, Trade Support
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- Full-time
Support the timely clearing of transactions within required regulatory timeframes, contributing to the firm's compliance with applicable rules and reporting obligations.
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Senior Financial/Compensation Analyst (16 month) Temp
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- $70,000 to $110,000 CAD / year
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Charles River Laboratories

Scientist in Immunochemistry

Montreal, QC, Canada

Salary: The hiring range for this position is $61.000 to $78.000/year. · Full-time

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Job details

Pay: Salary: The hiring range for this position is $61.000 to $78.000/year.
Job type: Full-time
Apply by: Nov 29, 2026
Experience: At least 3 years of experience as a Laboratory Analyst;
Posting language: English
Posted: Oct 30, 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 a Scientist for our Immunochemistry team located at the Ville St-Laurent facility, you will be responsible for the design, conduct and reporting of Laboratory Sciences studies efficiently, profitably and with the maximum scientific quality. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In This Role, Primary Responsibilities Include

Write and/or review study schedules, study plans, amendments and standalone and contributing Scientist draft and final reports;
Prompt verbal or written communication with Sponsors on study related business;
Oversee and coordinate all aspects of study related procedures, whether performed within the department or by service departments;
Review and approve raw data;
Notify the Senior Director, Laboratory Sciences and/or the Associate Scientific Director of technical problems or deviations from budgeted costs as soon as they become apparent;
Ensures that projects are performed according to Standard Operating Procedures (SOP) and Good Laboratory Practice (GLP) regulations and is aware of appropriate regulations, guidelines and guidance.

Key Elements

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

Holder of a Master or a PhD in Biochemistry, Immunology or any other Laboratory Science related discipline;
At least 3 years of experience as a Laboratory Analyst;
Outstanding organizational skills;
Good interpersonal and communication skills;
Strong problem-solving skills;
Work with precision, pay attention to detail and strive for quality work.

Role Specific Information

Location: 7170 rue Frederick-Banting, Saint-Laurent, QC, H4S 2A1;
Transportation: Free parking;
Annual bonus based on performance;
Schedule: Monday to Friday daytime;
Permanent position as of the hiring, full-time 37.5hrs per week;
Salary: The hiring range for this position is $61.000 to $78.000/year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications and location.

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 & 10 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.

237239

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More about this job

Responsibilities

Design, conduct, and report Laboratory Sciences studies while ensuring scientific quality, efficient execution, and compliance with SOPs and GLP regulations. Coordinate study procedures, communicate with sponsors, review raw data and reports, and promptly escalate technical issues or budget deviations.

Requirements

A master's or PhD in biochemistry, immunology, or another laboratory science discipline is required, along with at least three years of experience as a Laboratory Analyst. The role also requires strong organizational, interpersonal, communication, and problem-solving skills, as well as precision and attention to detail.

Skills

Immunochemistry
Biochemistry
Immunology
Laboratory Analysis
Study Design
Study Reporting
Raw Data Review
Sponsor Communication
Study Coordination
Good Laboratory Practice
Standard Operating Procedures
Regulatory Compliance
Organization
Interpersonal Communication
Problem-Solving
Attention To Detail

Benefits

Performance Bonus
Free Parking
Employee And Family Assistance Program
Telemedicine
Three Weeks Of Vacation
Ten Personal Days
Career Development Opportunities
Social Activities
Health And Wellness Coverage
Stock Purchase Program
Work-Life Balance Flexibility

Visa sponsorship

Not detected in the job text

Keywords

Immunochemistry
Biochemistry
Immunology
Laboratory Sciences
Laboratory Analyst
Preclinical Studies
Study Design
Study Plans
Study Schedules
Study Amendments
Scientific Reports
Raw Data
Sponsor Communication
Study Coordination
Standard Operating Procedures
Good Laboratory Practice
Regulatory Compliance
Scientific Quality
Budget Monitoring
Safety Assessment
Drug Development
Contract Research Organization
Biotechnology Research

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