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Added 17 mins ago
AH
Senior Advisor
Alberta Health Services
AB · Greater Edmonton Metropolitan Area
- Full-time
…stakeholders to build capability, understanding, and effective risk management. Communicate complex and sensitive information effectively, demonstrating cultural competence, professionalism…
Added 1 hour ago
L
Client Operations Specialist
Leads.io
Remote, Canada
- $50,000 to $57,500 CAD / year
- Full-time
- Remote
We’re looking for a Client Operations Specialist to own the end-to-end rollout and quality assurance of our direct client campaigns at Leads.io.
Added 3 hours ago
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- Full-time
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Added 4 hours ago
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Brussels, ON
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network technical specialist
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Bolton, ON
- Full-time
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Toronto, ON
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…and administrative activities, including receiving, inventory management, order fulfillment, shipping, and returns processing. You will work with the local team with support from remote…
Added 5 hours ago
UO
Intermediate Coordinator, Academic Program Management
University of Ottawa
Ottawa, ON · Lamoureux Hall
- Full-time
Reporting to the Senior Specialist of Academic Program Management, responsible for executing logistical activities related to the delivery of programs within a faculty, service or research…
Added 5 hours ago
UO
Intermediate Administrative Assistant, Dean's Office
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Ottawa, ON · Lamoureux Hall
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The Faculty of Education, along with its commitment to the promotion, advancement and dissemination of knowledge in the field of education in general, is actively involved in teacher…
Added 5 hours ago
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- $44 to $53 CAD / hour
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Added 5 hours ago
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Custodial Workload & Training Specialist
The University of British Columbia
Vancouver, BC
- $5,984 to $6,422 CAD / month
- Full-time
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Technical Documentation & BOM Specialist
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Ottawa, ON
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Added 5 hours ago
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Added 5 hours ago
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Sudbury, ON
Perform assessments in conjunction with Physician Specialist for individuals/injured workers with upper-extremity, lower-extremity, back and neck injuries, including some amputations.…
Added 5 hours ago
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Added 6 hours ago
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Senior Manager, Asset Management & Engineering
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Added 6 hours ago
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Specialist, Technical Training and Support
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The Specialist, Technical Training and Support role is a senior technical position within the Global Microbiology team functioning as an expert resource in microbiology across the…

Charles River Laboratories

Formulations Specialist

Montreal, QC, Canada

Salary: $28.50/hr. · Full-time

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Job details

Pay: Salary: $28.50/hr.
Job type: Full-time
Apply by: Nov 27, 2026
Posting language: English
Posted: Oct 28, 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 Formulations Specialist for our Formulations team at the Senneville location, you will prepare documentation and coordinate all activities related to assigned studies.

In This Role, Primary Responsibilities Include

Prepare the necessary study documents by ensuring that study plans, Standard Operating Procedures (SOP) and budget are respected.
Coordinate the activities of the assigned studies in accordance with the study plan and study schedule;
Act as a resource person to resolve technical problems (troubleshooting).
Participate in technical work in the laboratory when their help is required.
Participate in the writing and/or modifying of Standard Operating Procedures (SOP) when their help is required.
Participate in reception and shipping of packages (such as samples, test material and other products), register them, keep their inventory up to date and make sure of their availability during studies.

Job Description

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

College diploma (DEC) in Laboratory Science, Biotechnology, or another related field.
Minimum of two (2) years of experience in a regulated laboratory environment operating in compliance with Good Laboratory Practices (GLP).
Proficiency in both French and English, with strong verbal and written communication skills.
Strong organizational and prioritization skills in a fast-paced environment.
Excellent attention to detail and commitment to data quality and accuracy.
Ability to adapt quickly to changing priorities and manage multiple tasks simultaneously.
Strong communication and collaboration skills with both internal and external stakeholders.
Aptitude for mathematical calculations and data analysis.
Proficiency with computer applications and tools commonly used in a laboratory environment.

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, day schedule.
- Weekend rotation (4 days every 8 weeks).
- Holiday rotations.
Permanent position as of the hiring, full-time 37.5hrs per week.
Salary: $28.50/hr.

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 & 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.

237179

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More about this job

Responsibilities

Prepare study documentation and coordinate assigned studies in accordance with study plans, schedules, SOPs, and budgets. Troubleshoot technical issues, assist with laboratory work and SOP updates, and manage the receipt, shipment, registration, and inventory of study materials.

Requirements

Requires a college diploma in Laboratory Science, Biotechnology, or a related field, plus at least two years of experience in a regulated laboratory operating under GLP. Candidates must be proficient in French and English and demonstrate strong organization, attention to detail, communication, adaptability, mathematical ability, and laboratory computer skills.

Skills

Study Documentation
Study Coordination
Good Laboratory Practices
Standard Operating Procedures
Laboratory Troubleshooting
Laboratory Work
Inventory Management
Shipping And Receiving
Organization
Prioritization
Attention To Detail
Data Quality
Mathematical Calculations
Data Analysis
Communication
Task Management

Benefits

Performance-Based Annual Bonus
Employee And Family Assistance Program
Telemedicine And Access To Health Professionals
Three Weeks Of Vacation
Five Personal Days
Career Development Opportunities
Social Activities
Free Parking
Electric Vehicle Charging Station
Shuttle Service

Visa sponsorship

Not detected in the job text

Keywords

Formulations
Laboratory Science
Biotechnology
Good Laboratory Practices
Regulated Laboratory
Study Plans
Study Schedules
Standard Operating Procedures
Budget Compliance
Study Coordination
Technical Troubleshooting
Laboratory Work
Sample Handling
Test Materials
Shipping And Receiving
Inventory Management
Data Quality
Data Accuracy
Mathematical Calculations
Data Analysis
French
English

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