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Contract Science Jobs in Quebec (NOW HIRING)

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 ...

Science Will Win We will achieve impact by innovation and evidence based frameworks. Candor with Care We are open, honest and empathetic. Spring Health is proud to be an equal opportunity employer.

Science Will Win We will achieve impact by innovation and evidence based frameworks. Candor with Care We are open, honest and empathetic. Spring Health is proud to be an equal opportunity employer.

... contract negotiation cycle as needed. May lead the negotiations for some clients. * Lead Business Development marketing activities by attending trade/scientific shows and collaborating with the ...

Project, contract and risk management principles * Health and safety management Formal Education and/or Certification(s) and Experience * Minimum: college diploma in engineering, applied science or ...

CA$10.21K/mo

Faculty of Science Department : Physics and Computer Science Campus: Milton Employee Group: WLUFA ... This appointment is in accordance with the Contract Teaching Faculty and Part-time Librarians ...

CA$10.21K/mo

Faculty of Science Department : Physics and Computer Science Campus: Milton Employee Group: WLUFA ... This appointment is in accordance with the Contract Teaching Faculty and Part-time Librarians ...

CA$10.21K/mo

Faculty of Science Department : Physics and Computer Science Campus: Milton Employee Group: WLUFA ... This appointment is in accordance with the Contract Teaching Faculty and Part-time Librarians ...

CA$10.21K/mo

Faculty of Science Department : Physics and Computer Science Campus: Milton Employee Group: WLUFA ... This appointment is in accordance with the Contract Teaching Faculty and Part-time Librarians ...

CA$10.21K/mo

Faculty of Science Department : Physics and Computer Science Campus: Milton Employee Group: WLUFA ... This appointment is in accordance with the Contract Teaching Faculty and Part-time Librarians ...

CA$10.21K/mo

Faculty of Science Department : Physics and Computer Science Campus: Milton Employee Group: WLUFA ... This appointment is in accordance with the Contract Teaching Faculty and Part-time Librarians ...

CA$10.21K/mo

Faculty of Science Department : Physics and Computer Science Campus: Milton Employee Group: WLUFA ... This appointment is in accordance with the Contract Teaching Faculty and Part-time Librarians ...

CA$10.21K/mo

Faculty of Science Department : Physics and Computer Science Campus: Milton Employee Group: WLUFA ... This appointment is in accordance with the Contract Teaching Faculty and Part-time Librarians ...

CA$10.21K/mo

Faculty of Science Department : Physics and Computer Science Campus: Milton Employee Group: WLUFA ... This appointment is in accordance with the Contract Teaching Faculty and Part-time Librarians ...

Are you an Indigenous student in an administrative support, construction, environmental science ... Monitoring contracts (construction, property management, environmental) * Checking compliance with ...

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Contract Science information

What are the key skills and qualifications needed to thrive as a Contract Scientist, and why are they important?

To thrive as a Contract Scientist, you need a strong background in scientific research, data analysis, and subject-specific expertise, typically supported by at least a bachelor’s or master’s degree in a relevant field. Familiarity with laboratory information management systems (LIMS), statistical software, and relevant regulatory guidelines is essential. Excellent communication, adaptability, and project management skills help you navigate client relationships and shifting project requirements. These competencies ensure high-quality deliverables, regulatory compliance, and effective collaboration in a fast-paced, client-driven environment.

What are some common challenges faced by professionals in Contract Science, and how can they be addressed?

Professionals in Contract Science often encounter challenges such as managing multiple projects with tight deadlines, adapting to diverse client requirements, and maintaining clear communication across interdisciplinary teams. To address these, effective time management, staying organized with project tracking tools, and fostering transparent communication are essential. Building strong relationships with clients and colleagues, as well as continuously updating technical knowledge, can also help ensure project success and professional growth.

What is contract science?

Contract science refers to scientific research or services that are provided on a contractual basis, often by independent scientists, research firms, or specialized laboratories. These services can include conducting experiments, data analysis, product testing, or regulatory compliance studies for clients such as private companies, government agencies, or academic institutions. The goal is to deliver high-quality scientific results tailored to the specific needs of the client, usually within a set timeframe and budget. Contract science allows organizations to leverage specialized expertise and facilities without maintaining them in-house.

What is the difference between Contract Science vs Contract Pharmacist?

AspectContract ScienceContract Pharmacist
Required CredentialsBachelor's or Master's in Science, relevant certificationsPharmacy degree, state licensure, pharmacist license
Work EnvironmentLaboratories, research settings, clinical trialsPharmacy settings, hospitals, retail pharmacies
Employer & Industry UsagePharmaceutical companies, biotech firms, research institutionsHospitals, retail chains, healthcare providers

Contract Science professionals focus on research, data analysis, and scientific support within the pharmaceutical and biotech industries. In contrast, Contract Pharmacists primarily work in pharmacy settings, dispensing medications and providing patient care. While both roles may involve contractual work, their work environments, credentials, and industry applications differ significantly.

What are the most commonly searched types of Science jobs in Quebec? The most popular types of Science jobs in Quebec are:
What are popular job titles related to Contract Science jobs in Quebec? For Contract Science jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Contract Science jobs in Quebec look for? The top searched job categories for Contract Science jobs in Quebec are:
Infographic showing various Contract Science job openings in Quebec as of May 2026, with employment types broken down into 1% As Needed, 71% Full Time, 24% Part Time, 1% Temporary, and 3% Contract. Highlights an 80% Physical, 3% Hybrid, and 17% Remote job distribution.
Scientist I - Genetic Toxicology

Full-time

Medical, Retirement, PTO

Posted 7 days ago


Charles River Laboratories rating

8.2

Company rating: 8.2 out of 10

Based on 90 frontline employees who took The Breakroom Quiz

27th of 70 rated pharmaceutical


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 Summary

As a Scientist for our Genetic Toxicology team at the Senneville location, you will be involved in writing and/or reviewing study schedules, study plans, amendments, and reports. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

  • Write and/or review study schedules, study plans, amendments and standalone and contributing Scientist draft and final reports;
  • Prompt verbal or written communication with Sponsors on study related business;
  • Generate and distribute Client Interaction Reports (CIRs) in a timely manner;
  • Oversee and coordinate all aspects of study related procedures, whether performed within the department or by service departments;
  • Review and approve raw data;
  • Notify the Senior Director, Laboratory Sciences and/or the Associate Scientific Director of technical problems or deviations from budgeted costs as soon as they become apparent;
  • Ensures that projects are performed according to Standard Operating Procedures (SOP) and Good Laboratory Practice (GLP) regulations and is aware of appropriate regulations, guidelines and guidance.
Key Elements

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

  • Holder of a Master's degree in Immunology, or any other similar discipline, with a minimum of 3 years of experience in a position related to Biology;
  • PhD in Immunology or in any other discipline related to biology;
  • Proven experience in production management in a biotechnology or life sciences environment;
  • Strong knowledge in cell biology, organotypic models, and biological reagents;
  • Demonstrated expertise in project management, planning, and team leadership;
  • Excellent communication skills, organizational sense, and problem-solving orientation;
  • Ability to work independently, adapt to changing priorities, and maintain rigorous scientific standards;
  • Experience in continuous improvement initiatives and scaling strategies for small-scale bioproduction.

Assets:

 

  • Hands-on experience with organ-on-chip systems and hepatocyte cultures with primary and cell line;
  • Familiarity with animal component-free culture systems;
  • Strong trainer skills and ability to lead technical workshops;
  • Track record of scientific writing and publication in peer-reviewed journals;
  • Knowledge in genetic toxicology assessment, including micronucleus test, comet assays and sequencing.

Role Specific Information:

 

  • Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
  • 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;
  • 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);
  • 3 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.


What Charles River Laboratories employees say

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Benefits

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Get the full story on Breakroom


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About Charles River

Sourced by ZipRecruiter

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 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947