Associate Director, Immunology

BioTalent Canada; Laval; On-site; CAD 80,000 - 110,000; Full time

Job summary

Join a forward-thinking company as an Associate Director in Immunotoxicology, where you'll lead a talented team of scientists dedicated to advancing drug therapies. This role offers the opportunity to oversee critical Immunology studies, mentor emerging talent, and engage with sponsors to ensure best practices. With a strong commitment to employee development and a collaborative environment, this position is perfect for those passionate about making a difference in global health. Enjoy competitive benefits and a supportive workplace culture that values your contributions and fosters career growth.

Benefits

Health & Dental Coverage

Employee Assistance Program

Telemedicine Access

4 Weeks Vacation

10 Personal Days

Annual Bonus

Free Parking

In-House Advancement Opportunities

Social Activities

401K Plan

Qualifications

• 10+ years of experience in Immunology-related scientific roles.
• Strong expertise in Flow Cytometry and cell-based assays.

Responsibilities

• Oversee a team of scientists in Immunology studies.
• Prepare and approve study schedules and plans.

Skills

Flow Cytometry

Cell Based Assays

Analytical Skills

Organizational Skills

Communication Skills

Problem-Solving Skills

Education

Bachelor’s degree in Immunology

Master’s or Doctorate’s degree

Tools

BD Flow Cytometer

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.

As an Associate Director for our Immunotoxicology team located in Laval, you will undertake the role of overseeing a team of scientists who act as Study Director/Principal Investigator for the conduct of Immunology laboratory related studies, in many disciplines.

In this role, primary responsibilities include:

• Assist the Director, scientifically and administratively, to maximize team performance and quality through efficient organization of work;
• Supervise, mentor and manage a team of Immunology Scientists;
• Interact with study team, Study Directors, Quality Assurance Program, and management to take appropriate decisions and ensure actions are carried out;
• Prepare, review, and approve study schedules and study plans for Immunology studies in collaboration with Study Directors where appropriate;
• Supervise Scientists in the design and validation of cell based and flow cytometry assays; trouble-shoot assays when necessary;
• Interact with sponsors where appropriate to design studies and provide recommendations for best practices to follow;
• Act as the subject matter expert for any Immunology related topics, bought internally or externally;
• Review report and results to ensure the quality and accuracy of data.

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

• Bachelor’s degree in Immunology or related scientific field. Master’s or Doctorate’s degree is a definite asset;
• Minimum 10 years of relevant experience including a minimum of 7 years in a scientific position relevant to Immunology;
• Strong experience in Flow Cytometry, including multi-color panel design experience and cell based assays (ELISpot, etc.);
• Experience with the BD flow cytometer platforms; spectral flow cytometry experience is an asset;
• Excellent organizational and communication skills;
• Strong problem-solving and analytical skills;
• Ability to coach personnel;
• Experience in a Contract Research environment is an asset.

Role Specific Information:

• Transportation: Free parking on-site / Near the Montmorency subway;
• Annual bonus based on performance;
• Schedule: Daytime Monday to Friday;
• Permanent, full-time position as of the hiring.

Why Charles River?

• Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
• 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 Laboratories is an Equal Opportunity Employer – all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

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.