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Charles River Laboratories

Technician - Formulations

QC, Canada
Fleurimont, QC, Canada

Pay: Pay: 23.75$/hrs.
Job type: Full-time
Apply by: Oct 30, 2026
Posting language: English
Posted: Sep 30, 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

Technician – Formulations

As a Technician for our Formulations team in Sherbrooke, you will be responsible for preparing all the dosing substances in different concentrations and ensures the timely delivery of these dosing for administration.

In This Role, Key Responsibilities Include

In accordance with study plans, you will prepare the formulations for dosing either in solution, suspension capsule, or powder mixture. You will also handle samples under a Fume Hood using an aseptic method.
Execute the technical activities described in the procedures and study plans while respecting the Good Laboratory Practices (GLP).
Check the availability and prepare all required components related to its laboratory activities (literature, samples, solutions, material, equipment, etc.)

If you possess the following qualifications, we will train you in the rest:

A self-starter with a collaborative and positive attitude
Being able to work physically (lift up to 10 kg, walk, stand, stoop, etc.);
Understanding of written English
DEC in Science, Pharmaceutical Process Control, or Biopharmaceutical Production Technology; or an AEC in Biopharmaceutical Production. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Role Specific Information

Location: 1580 Rue Ida-Métivier, Sherbrooke, Qc, J1E 0B5.
Transportation: Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station.
Pay: 23.75$/hrs.

Evenings: $2.50;
Weekend: $2.75
Overtime: Time and a half;
Holidays: Double time

Schedule: Full time, permanent position (37.5 hours/week), depending on the needs, you may have to do overtime and work on weekend (Rotation).

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);
3 weeks’ Vacation & 5 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.

236394

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More about this job

Responsibilities

Prepare dosing formulations in specified concentrations and deliver them on time, including solutions, suspensions, capsules, and powder mixtures. Handle samples aseptically under a fume hood, follow study plans and procedures in compliance with GLP, and ensure required laboratory components and equipment are available.

Requirements

Applicants should have a DEC in Science, Pharmaceutical Process Control, or Biopharmaceutical Production Technology, or an AEC in Biopharmaceutical Production; equivalent education and experience may be accepted. The role also requires written English comprehension, a collaborative and positive attitude, initiative, and the ability to perform physical tasks such as lifting up to 10 kg, walking, standing, and stooping.

Skills

Formulation Preparation
Dosing Substance Preparation
Solution Preparation
Suspension Preparation
Capsule Preparation
Powder Mixture Preparation
Sample Handling
Fume Hood Operation
Aseptic Technique
Good Laboratory Practices
Following Study Plans
Attention To Detail
Collaboration
Physical Stamina
Written English Comprehension

Benefits

Free On-Site Gym
Employee And Family Assistance Program
Career Development Opportunities
Telemedicine Access
Three Weeks Of Vacation
Five Personal Days
Social Activities

Visa sponsorship

Not detected in the job text

Keywords

Formulations
Dosing Substances
Concentrations
Solutions
Suspensions
Capsules
Powder Mixtures
Fume Hood
Aseptic Method
Good Laboratory Practices
GLP
Study Plans
Laboratory Procedures
Sample Handling
Laboratory Equipment
Pharmaceutical Process Control
Biopharmaceutical Production
Science
Safety Assessment
Preclinical Drug Development
Contract Research Organization
CRO
Drug Therapies

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