Research Scientist - Immunogenicity

Charles River; Quebec; On-site; CAD 90,000 - 120,000; Full time

Benefits offered by this job

Annual bonus

Free gym on site

Employee and family assistance program

Vacation & 10 personal days

Job summary

Charles River is seeking a Research Scientist for the Immunogenicity team at the Senneville site. The role involves designing and conducting Laboratory Sciences studies, interpreting results, and producing high-quality reports.

You will coordinate all study activities and ensure accurate cost estimates, with regular communication with study directors and sponsors. Minimum qualifications include a Master or PhD in Immunology with 3–5 years in a scientific role, plus experience in 3D cell models

Qualifications

• Master in Immunology or PhD with 3–5 years in a scientific position.
• Experience with advanced cellular models (3D cell cultures) and computational biology.
• Experience with immunoassay techniques (ELISAs, ECLs, Luminex, flow cytometry, ELISpot).

Responsibilities

• 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.
• Prepare analytical procedures and assays.
• Conduct laboratory analysis and all related laboratory activities.
• Analyze scientific problems, troubleshoot analytical methods and technical issues.
• Write scientific documents, review and interpret the raw data.
• Promote timely communications with Study Directors and Sponsor.
• Ensure accuracy and completeness of project cost estimates.

Skills

Immunology

Scientific writing

Interpersonal communication

Problem-solving

Education

Master in Immunology or related discipline

PhD in Immunology or related discipline

Tools

ELISAs

ELISpot

Flow cytometry

MAPPS

DC maturation assays

Job description

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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 aResearch 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;
• Conduct laboratory analysis and all related laboratory activities;
• 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 scientist or technical problems as soon as they become apparent.

We are looking for the followingminimum 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 or PhD in Immunology or any biological related discipline;
• Experience in advanced cellular models (including 3D cell cultures and complex MPS), computational biology, and/or innovative technologies.
• Experience with predictive immunogenicity assays, such as MAPPS, proliferation assays, in vitro DC maturation assays, DC‑T cells co‑culture assays and peripheral tissue equivalent (PTE) is an asset.
• Experience with immunoassay techniques (ELISAs, ECLs, Luminex, flow cytometry, ELISpot) is an asset;
• Good interpersonal and communication skills;
• Strong problem‑solving skills;
• Work with precision, pay attention to detail and strive for quality work.

Role Specific Information

• Transportation: We offer a free shuttle service from the Sainte‑Anne‑de‑Bellevue train station and John Abbott College to the Senneville site. 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.

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.

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 [e-mail]. 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.

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