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Charles River Laboratories

Research Scientist - Immunogenicity

Montreal, QC, Canada

Salary: The hiring range for this position is $68,000 to $90,000 per year. · Full-time

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Job details

Pay: Salary: The hiring range for this position is $68,000 to $90,000 per year.
Job type: Full-time
Apply by: Dec 3, 2026
Experience: Holder of a Master in Immunology or any other related discipline with a minimum of 3 to 5 years’ experience working in a Scientific position;
Posting language: English
Posted: Nov 3, 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 Research Scientist for our Immunogenicity team at the Senneville location, you will serve as a Study Scientist or Principal Investigator responsible for the design, conduct of study related laboratory activities, interpretation and reporting of Laboratory Sciences studies efficiently, profitably and with the maximum scientific quality.

In This Role, Primary Responsibilities Include

Design, write, review, and edit study plans, amendments and study schedules that define and schedule all study activities;
Oversee and coordinate all aspects of study related Laboratory Sciences procedures, whether performed within the department or by service departments;
Prepare analytical procedures and assays;
Analyze scientific problems, troubleshoot analytical methods and technical issues;
Write scientific documents, review and interpret the raw data;
Write, review, and edit stand-alone contributing scientist draft and/or final reports that document all study related procedures and results;
Prompt verbal or written communications with Study Directors and/or Sponsor on study related business in a timely manner;
Ensure the accuracy and completeness of project cost estimates;
Notify the Principal Scientist and/or the Scientific Director of scientific or technical problems as soon as they become apparent.

Key Elements

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

Holder of a Master in Immunology or any other related discipline with a minimum of 3 to 5 years’ experience working in a Scientific position;
PhD in Immunology or any biological related discipline;
Experience with immunoassay techniques (ELISAs, ECLIAs, ACEs, Gyros, etc);
Experience in a regulated (GLP) environment is an asset;
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: 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 schedule;
Permanent position as of the hiring, full-time 37.5hrs per week;
Salary: The hiring range for this position is $68,000 to $90,000 per 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;
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);
4 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.

236378

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More about this job

Responsibilities

Design and coordinate study plans, schedules, laboratory procedures, and analytical assays, ensuring studies are conducted efficiently and to high scientific standards. Analyze and interpret data, troubleshoot scientific and technical issues, prepare study documentation and reports, communicate with study directors and sponsors, and monitor project cost estimates.

Requirements

Requires a master's degree in immunology or a related discipline and 3–5 years of experience in a scientific role; a PhD in immunology or a related biological discipline is also specified. Candidates should have experience with immunoassay techniques, with GLP experience considered an asset, as well as strong organizational, communication, problem-solving, precision, and quality-focused skills.

Skills

Immunology
Immunoassay Techniques
ELISA
ECLIA
ACE Assays
Gyros Assays
Study Design
Laboratory Sciences
Analytical Method Development
Troubleshooting
Scientific Data Interpretation
Scientific Writing
GLP Compliance
Project Cost Estimation
Organization
Communication

Benefits

Performance-Based Annual Bonus
Free On-Site Gym
Employee and Family Assistance Program
Career Development Opportunities
Telemedicine Access
Four Weeks of Vacation
Ten Personal Days
Free Parking
Electric Vehicle Charging Station
Shuttle Service

Visa sponsorship

Not detected in the job text

Keywords

Immunogenicity
Immunology
Laboratory Sciences
Study Scientist
Principal Investigator
Study Design
Study Plans
Study Schedules
Laboratory Procedures
Analytical Procedures
Assay Development
Immunoassays
ELISA
ECLIA
ACE Assays
Gyros Assays
Good Laboratory Practice
GLP
Scientific Data
Data Interpretation
Scientific Reporting
Raw Data Review
Method Troubleshooting
Technical Problem-Solving
Project Cost Estimation
Preclinical Drug Development
Safety Assessment
Contract Research Organization
Biotechnology Research

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