3175 offres d'emploi

Description du poste

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 Veterinary Technician for our Toxicology team in Laval, you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

• Evaluate and follow the health status of animals under veterinary supervision;
• Work closely with our veterinarians to prepare and perform treatment plans;
• Perform medical treatments, interventions, and diagnostic tests under veterinary supervision;
• Identify potential animal welfare issues and find solutions;
• Carry out behavioral assessments of animals and allocate necessary enrichments.

Key Elements

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

• College Diploma in Animal Health, Bioecology or any related Animal Science discipline;
• Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
• Good observation skills;
• Problem solving skills;
• Able to quickly adapt to last minute changes.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company

Role Specific Information

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Salary: $23.00/hrs;
• Premiums: Evening ($2.50), Weekend ($2.75), Overtime (Time and a half), Holidays (Double time);
• Annual bonus based on performance plan;
• Schedule: Daytime Monday to Friday with weekends rotation (1/2). Depending on the needs, you may have to do overtime and holidays;
• Permanent position as of the hiring, 37.5hrs per week.

Why Charles River ?

• We offer competitive benefits and advantages from day one to support your well-being;
• Paid development training;
• Employee and family assistance program;
• Access to a doctor and various health professionals (telemedicine);
• 3 weeks’ vacation & 5 Personal/Sick days per year;
• 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.

Informations sur l’entreprise

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.

Description du poste

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.

Vue d’ensemble du poste

As a Histology Technician for our team located in Laval, you will be responsible for preparing tissues for microscopic analysis. 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:

• Perform histology activities such as trimming, decalcification, processing, embedding, cutting, scanning, and staining;
• Prepare necessary material requested by procedures;
• Operate necessary laboratory equipment;
• Prepare chemical reagents;
• Prepare shipment and packing of specimens.

Éléments clés

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

• Collegial Diploma in Science, Biotechnology, or any other related field;
• Able to demonstrate a high level of attention to details;
• Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).

Informations spécifiques au rôle

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Salary: Starting at $21.50/hrs;
• Annual bonus based on performance plan;
• Schedule: Days & Evening shifts. Depending on the needs you must be available to work during days, evening, weekends, and holidays. Regular working hours are between 8am to 4:15 pm, but may be subject to change depending on current studies;
• Permanent position as of the hiring, full-time 37.5hrs per week.

Pourquoi Charles River ?

• We offer competitive benefits and advantages from day one to support your well-being;
• Paid development training;
• Employee and family assistance program;
• Access to a doctor and various health professionals (telemedicine);
• Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
• 3 weeks’ vacation & 5 sick/personal days per year;
• 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.

À propos de 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.

À propos de 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.

Ce que nous offrons

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.

Description du poste

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 Neuroscience Scientist for our Toxicology team located in Laval, you will be overseeing study conduct of preclinical efficacy and/or toxicology studies. Combined with neuroscience expertise and MRI‑guided dosing responsibilities, the role expands to include scientific leadership in CNS models, technical oversight of neuroimaging, and precision delivery into the brain or CNS structures. 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:

• Design and oversee with prospective and current clients MRI-guided targeting strategies for CNS delivery and support commercial groups in the preparation of statement of work;
• Perform MRI-guided dosing in collaboration with the surgeon team, ensure accurate placement to minimize off-target dose administration;
• Develop and optimize MRI protocols and targeting methodologies and contribute to innovation in CNS drug delivery techniques;
• Function as an independent Study Director in accordance with the applicable Good Laboratory Practice regulations (GLPs);
• Designs, writes, reviews and edits, as necessary, Study Plans, amendments and study schedules that define and schedule all study activities;
• Oversees and coordinates all aspects of study procedures, whether performed within the department or by service departments;
• Ensures that projects are performed according to Standard Operating Procedures and Good Laboratory Practice regulations and is aware of appropriate regulations, guidelines and guidances;
• Writes, reviews, and edits, as necessary, draft or final reports that document all study related procedures and results;
• Prompt verbal or written communication with Sponsors on study related business;
• Oversees and coordinates study conduct (MRI protocol and Study Plan development, technical guidance, and reporting).

Key Elements

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

• Master’s or Doctorate in Neuroscience or any other related discipline;
• Experience related to MRI (Magnetic Resonance Imaging) and theoretical & practical knowledge of the subject are preferred;
• MRI-related targeting dosing is an asset;
• Good interpersonal and communication skills;
• Strong problem-solving skills.

Role Specific Information:

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Annual bonus based on performance;
• Schedule: Monday to Friday, 8:00 am to 4:15 pm;
• Hybrid position – half on-site & half remote;
• 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;
• Paid development training;
• 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.

À propos

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.

Benefits

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.

Qui sommes-nous ?

At Schneider Electric, we shape the future by electrifying, automating, and digitizing the world around us.
With a presence in more than 100 countries, we bring together 160,000 talents driven by a shared mission: making energy smarter, more efficient, and more sustainable - for everyone. We enable buildings, factories, data centers, and infrastructure to operate as true open and interconnected ecosystems by combining energy technologies, advanced automation, artificial intelligence, software, and digital services. With €38 billion in revenue in 2024 and strong growth fueled by innovation, we are among the most sustainable and influential companies in the industry.
Our last twelve months' revenue has reached €39.32billion, confirming our exceptional momentum.

Que défendons-nous ?

Our IMPACT values - Inclusion, Mastery, Purpose, Action, Curiosity, and Teamwork - define who we are.
They guide how we collaborate, learn, innovate, and grow together. At Schneider Electric, we believe in an environment where everyone can be themselves, find purpose in their work, develop their skills, and thrive in a culture built on well-being, diversity, and high performance.

Quel est le poste ?

For our Brossard, Québec Plant, we are looking for a Mechanical Designer Reporting to the Mechanical Engineering Supervisor, the selected candidate will work closely with the engineering team on various electrical power distribution projects aimed at measuring, controlling, and protecting equipment. This role stands out for its dynamic nature and wide variety of challenges.

It is ideal for someone who wants to avoid routine, enjoys working in a constantly evolving environment, and appreciates collaborating with many different stakeholders.

Principales responsabilités

• Design and develop 3D mechanical assemblies and components to customize Schneider solutions according to customer specifications.
• Ensure all designs meet applicable industry standards, including CSA, UL, ANSI, ISO, and other relevant certifications.
• Generate high-quality 2D drawings and prepare complete Bills of Materials (BOMs) within required project timelines.
• Provide hands-on technical support to the assembly line, addressing questions and resolving issues to maintain smooth production workflows.
• Collaborate closely with cross-functional teams including Engineering, Quality, and Supply Chain to ensure product excellence and on-time delivery.

Pourquoi vous ?

Are you passionate about innovation and driven by the desire to make a difference? Are you a confident and committed professional, ready to contribute to the success of a company that stands out both locally and internationally? Do you enjoy achieving your goals, collaborating with others, and fully investing yourself in everything you do?

Plus, you have the following qualities and certifications:

Qualités et certifications

• Bachelor's degree in mechanical engineering, or a Technical Diploma (DEC) in Mechanical Engineering with equivalent experience.
• 1 to 3 years of experience in a similar mechanical design or engineering role.
• Proficiency with ProE/Creo and PDM/Windchill (or equivalent CAD/PDM systems); experience with AutoCAD is also an asset.
• Strong knowledge of sheet-metal and copper component fabrication processes.
• Solid technical project management skills, with the ability to manage priorities in a fast-paced environment.
• Excellent communication, teamwork, and leadership abilities.
• Basic understanding of electrical principles, including reading technical schematics and awareness of electrical hazards.
• Bilingual in French and English (intermediate level) to support national and international collaboration with partners.
• Experience in designing electrical distribution equipment is considered an asset.

Pourquoi nous ?

At Schneider Electric, we believe that the true strength of our company lies in the talent of our people.
Our commitment to diversity, equity, inclusion, and sustainability is at the heart of everything we do. Thanks to these values, we innovate to deliver technologies that empower everyone to live better - everywhere, for all, and at all times. Bring your engineering talent to a team that values quality and innovation - apply today!

Égalité des chances

At Schneider, we believe that every employee is a talent who deserves equal opportunities.
This means you matter.
Every individual needs to feel valued, supported, and treated fairly to do their best work.

Nos Total Rewards

Our Total Rewards is our way of saying: "We see you.
We value you".
It's more than just pay and benefits- it's a meaningful investment in you.
It is designed for you to perform, grow, feel safe, and elevate your potential to shine as an impact maker.

The expected pay range is CAD 64,000 - CAD 96,000 per year.
This pay range includes base pay and short-term incentives. For Ontario applicants, this posting complies with provincial law which does not require disclosure of the pay range.
Inquiries regarding the pay range can be directed to the recruiting / hiring manager.

Schneider Electric est là au moment où vous en avez le plus besoin

Our Total Rewards package outlines all the benefits and support you'll enjoy as part of the Schneider Electric team:

Prendre soin de vous et de votre famille

We ensure you feel secure with benefits that help you and your family thrive: insurance coverage for health, inclusive of medical, dental, vision, basic life, accident, and disability insurance; telemedicine program; paid family leaves; parental and care leave; employee assistant program with mental, family, and legal counselling and flexible work arrangements.

Investir et planifier votre avenir

We help you plan and invest for the future with competitive pay and programs: base salary; incentive plans; employee share ownership plan; retirement plan with employer pension match.

Développer vos compétences et votre carrière

We commit to helping you grow with ongoing performance and development conversations, Senior Talent Program, global career opportunities, access to our Schneider Career Hub for new positions, projects, and mentors, and learning platforms like Coursera to equip you with the skills for today and tomorrow.

Travailler en équipe

We encourage teaming up through project opportunities on the Schneider Career Hub, smart ways to collaborate, celebrating contributions via a recognition program (including service anniversary), sharing your voice in our engagement survey, and fostering an inclusive, caring workplace.

Soutenir votre communauté

We make a difference in your community with volunteer leave, programs through the Schneider Electric Foundation, and initiatives that support youth education.

Rejoignez-nous pour faire un IMPACT

When you are thinking about joining a new team, culture matters.
At Schneider Electric, our values and behaviors are the foundation for creating a great culture to support business success.
We believe that our IMPACT values - Inclusion, Mastery, Purpose, Action, Curiosity, Teamwork - starts with us. IMPACT is also your invitation to join Schneider Electric where you can contribute to turning sustainability ambition into actions, no matter what role you play.
It is a call to connect your career with the ambition of achieving a more resilient, efficient, and sustainable world.

We are looking for IMPACT Makers; exceptional people who turn sustainability ambitions into actions at the intersection of automation, electrification, and digitization.
We celebrate IMPACT Makers and believe everyone has the potential to be one. Become an IMPACT Maker with Schneider Electric - apply today!

€40 billion global revenue +9% organic growth 150 000+ employees in 100+ countries

Candidature

You must submit an online application to be considered for any position with us.
This position will be posted until filled.

Inclusion et sécurité

Schneider Electric aspires to be the most inclusive and caring company in the world, by providing equitable opportunities to everyone, everywhere, and ensuring all employees feel uniquely valued and safe to contribute their best.
We mirror the diversity of the communities in which we operate, and 'inclusion' is one of our core values.
We believe our differences make us stronger as a company and as individuals and we are committed to championing inclusivity in everything we do.

Éthique et conformité

At Schneider Electric, we uphold the highest standards of ethics and compliance, and we believe that trust is a foundational value.
Our Trust Charter is our Code of Conduct and demonstrates our commitment to ethics, safety, sustainability, quality and cybersecurity, underpinning every aspect of our business and our willingness to behave and respond respectfully and in good faith to all our stakeholders.
You can find out more about our Trust Charter here

Schneider Electric is an Equal Opportunity Employer.
It is our policy to provide equal employment and advancement opportunities in the areas of recruiting, hiring, training, transferring, and promoting all qualified individuals regardless of race, religion, color, gender, disability, national origin, ancestry, age, military status, sexual orientation, marital status, or any other legally protected characteristic or conduct.

À propos de Charles River

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.

Description du poste

As a Study Specialist for our Clinical Pathology team at the Laval location, you will assist and oversees the technical team during the conduct of the study including organization of the work and technical support according to Good Laboratory Practice (GLP).

In this role, primary responsibilities include:

• Work closely with study directors on all aspects of assigned studies;
• Perform the follow up of studies by preparing the appropriate documentations;
• Oversees technical teams and act as the main contact for problem solving issues;
• Oversees sample shipment preparation to archives and management of samples during finalization;
• Perform follow ups and verification of studies;
• Review raw data and complete Quality Assurance inspection reports;
• Write and review deviation reports, when necessary;
• Ensure that daily, weekly, monthly instrument calibration and maintenances are done properly.

Qualifications minimales

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

• Bachelor’s degree in Biology or any other discipline related to biological sciences;
• 5 years of experience as a Clinical Pathology Technician;
• Good knowledge and application of GLP;
• Detail oriented and meticulous;
• Ability to work under time constraint and adapt to change;
• Demonstrate flexibility and ability to work independently.

Informations propres au poste

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Salary: Starting at 28$/hrs;
• Annual bonus based on performance;
• Schedule: Monday to Friday, daytime schedule. Depending on the business needs, you may have to do overtime;
• Permanent position as of the hiring, full-time 37.5hrs per week.

Pourquoi 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!

À propos de la sécurité et de l’évaluation

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.

À propos de Charles River

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.

Ce que nous offrons

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.

Description du poste

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.

Présentation du poste

As a Technician for our Necropsy team located in Laval, you will mainly be responsible for performing the post-mortem examination of animals while following the ethical regulations and directives from study plans. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

• Dissecting and evaluating animal tissues for pathologists;
• Weigh and document all abnormalities of the organs;
• Euthanize animals prior to performing the necropsy.

Qualifications minimales

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

• Collegial Diploma in Animal Health or any other Biology related field;
• Bachelor’s degree in biology or any other Animal Science related field;
• Dissection experience (asset);
• Good observation skills;
• Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Informations spécifiques au rôle

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Salary: $22/hrs;
• Annual bonus based on performance;
• Schedule: Daytime schedule, Monday to Friday. Depending on the needs, you may have to do weekends rotations and overtime;
• Permanent position as of the hiring, full-time 37.5hrs per week.

Pourquoi Charles River ?

• We offer competitive benefits and advantages from day one to support your well-being;
• Paid development training;
• 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.

À propos de 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.

À propos de 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.

Description du poste

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.

Vue d’ensemble du poste

As a Laboratory Clerk for our Histology team at the Laval location, you will provide general technical support within the departments.

In this role, primary responsibilities include:

• Prepare the required material needed to perform histology activities;
• Prepare specimens for storage and/or archiving;
• Receive and store chemicals, biological matrices, disposable material and keep inventories up to date;
• Keep the working area and storage room clean and organized.

Qualifications

If you have the following qualifications, we'll train you for the rest:

• High School diploma;
• Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
• Ability to work under time constraints and adapt to change;
• Demonstrate flexibility and ability to work independently.

Informations propres au poste

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Salary: $17.50/hr;
• Annual bonus based on performance;
• Schedule: Monday to Friday daytime. Depending on the business needs, you might have to do overtime;
• Permanent position as of the hiring, full-time 37.5hrs per week.

Pourquoi 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.

À propos

À propos de 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.

À propos de 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.

Avantages

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.

Description du poste

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 Veterinary Technician for our Toxicology team in Laval, you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

• Evaluate and follow the health status of animals under veterinary supervision;
• Work closely with our veterinarians to prepare and perform treatment plans;
• Perform medical treatments, interventions, and diagnostic tests under veterinary supervision;
• Identify potential animal welfare issues and find solutions;
• Carry out behavioral assessments of animals and allocate necessary enrichments.

Éléments clés

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

• College Diploma in Animal Health, Bioecology or any related Animal Science discipline;
• Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
• Good observation skills;
• Problem solving skills;
• Able to quickly adapt to last minute changes.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company

Informations spécifiques au rôle

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Salary: $23.00/hrs;
• Premiums: Evening ($2.50), Weekend ($2.75), Overtime (Time and a half), Holidays (Double time);
• Annual bonus based on performance plan;
• Schedule: Daytime Monday to Friday with weekends rotation (1/2). Depending on the needs, you may have to do overtime and holidays;
• Permanent position as of the hiring, 37.5hrs per week.

Pourquoi Charles River ?

• We offer competitive benefits and advantages from day one to support your well-being;
• Paid development training;
• Employee and family assistance program;
• Access to a doctor and various health professionals (telemedicine);
• 3 weeks’ vacation & 5 Personal/Sick days per year;
• 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.

À propos de 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.

À propos de 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.

Description du poste

Je suis propriétaire à Côte Saint-Luc, Québec, et je cherche à embaucher une femme/homme de ménage fiable pour m’aider à accomplir diverses tâches à la maison. Le poste offre un taux horaire de $20, et je suis impatient(e) de trouver quelqu’un qui prend fierté dans son travail.

Les principales responsabilités incluront le nettoyage de la salle de bain afin qu’elle soit impeccable et désinfectée. Le maintien de la propreté dans les pièces générales est également essentiel, car j’apprécie un environnement bien rangé et accueillant. La cuisine nécessitera un nettoyage approfondi, notamment les comptoirs et les appareils électroménagers. De plus, j’aimerais que le/la candidat(e) aide au nettoyage du réfrigérateur, en veillant à ce qu’il soit organisé et hygiénique.

Une grande attention aux détails est cruciale pour ce poste, car je crois qu’il est important de maintenir un espace de vie propre et sain.

Si vous êtes intéressé(e) par cette opportunité et que vous pensez correspondre aux exigences, n’hésitez pas à m’envoyer un message. Je me réjouis de vos nouvelles et d’avoir peut-être le/la plaisir de vous accueillir chez moi. Merci d’avoir considéré ce poste ! Veuillez visiter pour consulter les détails complets et postuler. Il y a beaucoup d’emplois parmi lesquels choisir !

Tâches et responsabilités

• Nettoyage de la salle de bain (impeccable et désinfectée)
• Maintenir la propreté dans les pièces générales
• Nettoyer soigneusement la cuisine (comptoirs et appareils)
• Aider au nettoyage du réfrigérateur (organisé et hygiénique)
• Assurer une attention aux détails pour maintenir un espace de vie propre et sain

À propos de Charles River

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.

Description du poste

As a Laboratory Instrument Specialist for our Equipment Services team at the Laval location, you will deal with issues related to the support of the equipment and instruments used and will be a resource to the technical group. You’ll also need basic scientific knowledge to help you understand the operation of the instrument and make a correct diagnosis.

In this role, primary responsibilities include:

• Participate in the setup, configuration and qualification of the instrumentation necessary to implement the tests in the laboratory;
• Understand the interactions between the different components that make up the instrument in order to target the cause of a problem;
• Participate in instrument software validations in a supporting role for technical expertise or workflow improvement;
• Support the management of requests for equipment, instruments, or supplies for studies;
• Participate in maintaining SOP’s for equipment and instruments.

Qualifications

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

• Minimum of a Collegial diploma in Biology, Biochemistry or any other related field;
• At least 1 to 2 years of experience in one or more of these areas: Biochemistry, Analytical Chemistry, maintenance and certification, and troubleshooting of LCMS & HPLC systems;
• Have knowledge in mathematics and statistics to understand the use of instruments (standard curves, standard deviation, % deviation, concentration calculation, etc.);
• Have scientific knowledge to understand the use of instruments in order to make an accurate diagnosis (different types of detection, sensitivity, precision, interference, contamination, background noise, etc.);
• Demonstrate excellent teamwork efforts and communication;
• Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).

Informations spécifiques au rôle

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Annual bonus based on performance;
• Schedule: Monday to Friday between 8am to 4:15pm. Depending on the business needs, you may have to do overtime;
• Permanent position as of the hiring, full-time 37.5hrs per week.

Pourquoi Charles River ?

• We offer competitive benefits and advantages from day one to support your well-being;
• Paid development training;
• 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!

Si vous êtes intéressé

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.

À propos de 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.

À propos de 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.

Description du poste

Bonjour, amoureux des animaux ! Je m’appelle Kemmah et je suis propriétaire d’animaux vivant à Le Vieux-Longueuil, Québec. Je cherche une personne fiable et passionnée pour s’occuper de mes chats et de mes chiens bien-aimés. J’ai besoin de quelqu’un qui aime les animaux et qui peut leur offrir une attention et des soins excellents.

Vos responsabilités incluront : les nourrir, jouer avec eux et veiller à leur sécurité pendant mon absence. Si vous avez de l’expérience en promenade de chiens, c’est un excellent plus, car mes chiens adorent leurs promenades quotidiennes.

Le tarif est de 17 $ par jour pour vos services.

Je cherche quelqu’un qui pourra établir une relation amicale et de confiance avec mes compagnons à quatre pattes tout en les gardant heureux et à l’aise. Si vous êtes intéressé par cette opportunité et que vous répondez aux critères, n’hésitez pas à m’envoyer un message. J’aimerais vous entendre et discuter de la façon dont vous pouvez convenir parfaitement à notre famille.

Veuillez visiter pour voir les détails complets et pour postuler. Beaucoup d’emplois à choisir !

Description du poste

Intelcom | Dragonfly

With more than 100 sorting stations and operations across three continents, Intelcom | Dragonfly is Canada’s leader in last-mile logistics. Our vision is clear: to deliver fast, accurate, and reliable service powered by cutting-edge technology.

Une fonction stratégique au cœur des opérations logistiques

Responsabilités

Gestion opérationnelle

• Identify, analyze, and validate stakeholder needs and process.
• Provide support and training to stakeholders (particularly HR) to enhance the overall user experience.
• Configure, review, and maintain Workday system, including business process design, security, and audit implementation.
• Assist in defining objectives, scope, timelines, phases, milestones, and in establishing budgets for HR platform projects and continuous improvement initiatives.

Projets et amélioration continue

• Work on projects impacting multiple teams or departments.
• Create and maintain process flow, configuration, operational, and user documentation.
• Identify opportunities and areas for business process improvement to drive value and increase efficiency within technology tools, while ensuring data quality, consistency, and standardization.
• Monitor new features released by Workday and recommend appropriate adoption and deployment plans.

Données et analyses

• Document business and functional requirements, translating them into technical specifications while incorporating data governance and data quality rules (validation, standardization, controls).
• Establish and monitor data quality metrics, produce regular analysis, and collaborate with HR teams to improve data entry and data management practices.

Gouvernance et sécurité

• Ensure compliance with existing security policies regarding data integrity, confidentiality, and availability.
• Identify and document integration requirements for applications within Workday, and ensure data consistency and alignment across systems (payroll, finance, IT).
• Participate in root cause analysis of data flow issues, recommend and implement sustainable solutions, including automated controls and preventive mechanisms.

Qualifications

• 3 to 5 years' experience as a HR IS Business or Functional Analyst
• At ease on Data Quality topic, analysis and audit
• Bachelor's degree in IT, HR or related field
• Workday knowledge
• PMI-PBA certification, an asset
• The role involves daily (or regular) communication with pan-Canadian stakeholders.
• Excellent oral and written communication skills
• Ability to analyze and synthesize information
• Ability to influence and negotiate
• At ease and autonomous in a growth environment
• Organizational skills, attention to detail and good judgment are a must
• Experience in the Transport/Logistics sector, an asset

Pourquoi nous joindre ?

At Intelcom | Dragonfly, you’ll thrive in a flexible and stimulating environment, surrounded by passionate talent. You’ll also enjoy a wide range of benefits:

• On-site gym with a personal trainer

• Employer-provided lunch of your choice

• Comprehensive group insurance

• Group RRSP plan

• Care & Well‑Being Activities

• Partial reimbursement for public transportation

• Employee Assistance Program

…and much more.

This position has been opened to address a genuine organizational need within the company.

At Intelcom | Dragonfly, we move forward guided by strong values: collaboration, innovation, excellence, and responsibility.

We embrace diversity, ensure equity, and foster a true sense of belonging.

Accommodation measures are available for individuals with disabilities throughout our recruitment process, in compliance with the law. Please let us know if you have any specific needs.

Description du poste

Pour notre usine de Brossard, Québec, nous recherchons un ingénieur en conception électrique. Rattaché au superviseur du génie électrique, le/la candidat(e) retenu(e) travaillera en étroite collaboration avec l’équipe d’ingénierie sur divers projets de distribution d’énergie électrique visant à mesurer, contrôler et protéger les équipements. Ce rôle se distingue par sa nature dynamique et la grande variété de défis. Il est idéal pour une personne qui souhaite éviter la routine, qui aime travailler dans un environnement en constante évolution et qui apprécie de collaborer avec de nombreuses parties prenantes.

Ce que vous ferez

• Effectuer des revues techniques de projets et s’assurer de la conformité à toutes les exigences.
• Concevoir des schémas électriques détaillés : schémas unifilaires, schémas de commande, schémas de câblage et dessins d’assemblage.
• Réaliser l’ingénierie détaillée selon les besoins des clients, les spécifications, les normes applicables (CSA, UL, ANSI) et les lignes directrices internes.
• Préparer et valider des documents techniques : listes de matériaux, listes de composants et nomenclatures (BOM).
• Sélectionner les composants électriques requis pour la fabrication des panneaux et de l’équipement.
• Gérer efficacement le temps afin de respecter les échéances des projets (dessins d’approbation, lancement en production, etc.).
• Fournir un support à la fabrication : répondre aux questions liées aux projets pendant l’assemblage et les tests (mécanique/câblage/tests) et assurer la cohérence de la conception tout au long de la production.

Pourquoi nous?

Chez Schneider Electric, nous croyons que la force réelle de notre entreprise réside dans le talent de nos employés. Notre engagement envers la diversité, l’équité, l’inclusion et la durabilité est au cœur de tout ce que nous faisons. Grâce à ces valeurs, nous innovons pour offrir des technologies qui permettent à chacun de vivre mieux — partout, pour tous et à tout moment.

Pourquoi vous?

Êtes-vous passionné(e) par l’innovation et motivé(e) par le désir de faire une différence? Êtes-vous un(e) professionnel(le) confiant(e) et engagé(e), prêt(e) à contribuer au succès d’une entreprise qui se démarque à la fois localement et à l’international? Aimez-vous atteindre vos objectifs, collaborer avec les autres et vous investir pleinement dans tout ce que vous faites? De plus, vous avez les qualités et certifications suivantes :

Qualités et certifications

• Baccalauréat ès sciences en génie électrique ou expérience équivalente
• Membre ingénieur de l’OIQ. (atout)
• Expérience pertinente dans la conception détaillée d’équipements électriques
• Expérience pratique avec un logiciel de CAO électrique (See Electrical / See XP est un atout)
• Compétences en gestion de projet technique et en priorisation
• Capacité à résoudre et éliminer les problèmes techniques
• Expérience en conception de panneaux de distribution / armoires de contrôle (atout)
• Connaissance des normes et codes applicables (ANSI/IEEE, CSA, Hydro-Québec, etc.) est un atout
• Bilingue en français et en anglais (niveau intermédiaire requis pour la communication nationale et internationale avec nos partenaires)

Description du poste

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 Data Reviewer for our Clinical Pathology team at the Laval location, you will verify data for completeness and Good Laboratory Practice (GLP) compliance, and you will promote awareness of best practices related to data collection.

In this role, primary responsibilities include:

• Perform review of supporting data and complex clinical pathology data;
• Ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP) and the Institutional Animal Care and Use Committee (IACUC) rules.

Qualifications minimales

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

• College diploma in science;
• Minimum of 3 years’ experience working in a Good Laboratory Practices (GLP) environment;
• Ability to work under time constraint and adapt to change;
• Demonstrate flexibility and ability to work independently.

Informations spécifiques au rôle

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Salary: $23/hrs;
• Annual bonus based on performance;
• Schedule: Monday to Friday, daytime schedule. Depending on the business needs, you may have to do overtime;
• Permanent position as of the hiring, full-time 37.5hrs per week.

Pourquoi 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.

À propos de 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.

À propos de 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.

Ce que nous offrons

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 — Animal Health Technician (Toxicology) à Laval

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.

Présentation du poste

As an Animal Health Technician for our Toxicology team in Laval, you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

• Collection of biological samples (blood, urine, etc.);
• Data collection (body weight, food consumption, clinical signs, etc.);
• Injections (subcutaneous, intramuscular, etc.);
• Animal contention;
• Animal room cleaning.

Qualifications minimales

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

• College Diploma in Animal Health - New graduates are welcome, no working experience required!;
• College Diploma in Bioecology, Biology, Biotechnology, or any other related disciplines with experience in injections and/or blood collection on animals;
• Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
• Good observation skills;
• Problem solving skills.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Informations spécifiques au rôle

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Salary: Starting at 23.50$/hrs. Opportunity to start at higher level and higher salary with specific research experience;
• Premiums: Weekends ($2.75), Overtime (time and a half), Holidays (double time);
• Annual bonus based on performance;
• Schedule: Flexible schedule, the candidate must be available during the day, evenings and weekends. Depending on the needs of the company, you may be required to work overtime, holidays and night shifts;
• Permanent position as of the hiring, full-time 37.5hrs per week.

Pourquoi 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.

À propos de 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.

À propos de 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.

Ce que nous offrons

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.

À propos de Charles River

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.

Présentation du poste

As an Animal Health Technician for our Toxicology team in Laval, you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

• Collection of biological samples (blood, urine, etc.);
• Data collection (body weight, food consumption, clinical signs, etc.);
• Injections (subcutaneous, intramuscular, etc.);
• Animal contention;
• Animal room cleaning.

Qualifications minimales

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

• College Diploma in Animal Health - New graduates are welcome, no working experience required!;
• College Diploma in Bioecology, Biology, Biotechnology, or any other related disciplines with experience in injections and/or blood collection on animals;
• Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
• Good observation skills;
• Problem solving skills.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Informations spécifiques au rôle

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Salary: Starting at 23.50$/hrs. Opportunity to start at higher level and higher salary with specific research experience;
• Premiums: Weekends ($2.75), Overtime (time and a half), Holidays (double time);
• Annual bonus based on performance;
• Schedule: Flexible schedule, the candidate must be available during the day, evenings and weekends. Depending on the needs of the company, you may be required to work overtime, holidays and night shifts;
• Permanent position as of the hiring, full-time 37.5hrs per week.

Pourquoi 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.

À propos de 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.

À propos de 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

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 Laboratory Clerk for our Sample Management team at the Laval location, you will provide general technical support within laboratories on company premises, as required. You will carry out duties according to Good Laboratory Practice (GLP) at all times.

In this role, primary responsibilities include:

• Receive or pick up samples from the facility;
• Prepare the required materials for the study conduct;
• Keep the samples well organized within the freezers and ensure proper documentation;
• Perform maintenance/cleaning of the fridges and freezers;
• Keep the working area clean and organized.

If you have the following qualifications, we'll train you for the rest:

• Minimum High School Diploma is required;
• Good organizational, interpersonal and communication skills;
• Detail oriented and meticulous.

Role Specific Information

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Salary: $17.50/hrs;
• Annual bonus based on performance;
• Schedule: Monday to Friday, 8am to 4:15pm. Depending on the business needs, you will have to do overtime;
• 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;
• Paid development training;
• 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.

Description du poste

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 Laboratory Clerk for our Sample Management team at the Laval location, you will provide general technical support within laboratories on company premises, as required. You will carry out duties according to Good Laboratory Practice (GLP) at all times.

In this role, primary responsibilities include:

• Receive or pick up samples from the facility;
• Prepare the required materials for the study conduct;
• Keep the samples well organized within the freezers and ensure proper documentation;
• Perform maintenance/cleaning of the fridges and freezers;
• Keep the working area clean and organized.

Qualifications

If you have the following qualifications, we'll train you for the rest:

• Minimum High School Diploma is required;
• Good organizational, interpersonal and communication skills;
• Detail oriented and meticulous.

Role Specific Information

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Salary: $17.50/hrs;
• Annual bonus based on performance;
• Schedule: Monday to Friday, 8am to 4:15pm. Depending on the business needs, you will have to do overtime;
• 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;
• Paid development training;
• 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.

Ce que nous offrons

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.

Description du poste

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 Neuroscience Scientist for our Toxicology team located in Laval, you will be overseeing study conduct of preclinical efficacy and/or toxicology studies. Combined with neuroscience expertise and MRI‑guided dosing responsibilities, the role expands to include scientific leadership in CNS models, technical oversight of neuroimaging, and precision delivery into the brain or CNS structures. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

Responsabilités principales

In this role, primary responsibilities include:

• Design and oversee with prospective and current clients MRI-guided targeting strategies for CNS delivery and support commercial groups in the preparation of statement of work;
• Perform MRI-guided dosing in collaboration with the surgeon team, ensure accurate placement to minimize off-target dose administration;
• Develop and optimize MRI protocols and targeting methodologies and contribute to innovation in CNS drug delivery techniques;
• Function as an independent Study Director in accordance with the applicable Good Laboratory Practice regulations (GLPs);
• Designs, writes, reviews and edits, as necessary, Study Plans, amendments and study schedules that define and schedule all study activities;
• Oversees and coordinates all aspects of study procedures, whether performed within the department or by service departments;
• Ensures that projects are performed according to Standard Operating Procedures and Good Laboratory Practice regulations and is aware of appropriate regulations, guidelines and guidances;
• Writes, reviews, and edits, as necessary, draft or final reports that document all study related procedures and results;
• Prompt verbal or written communication with Sponsors on study related business;
• Oversees and coordinates study conduct (MRI protocol and Study Plan development, technical guidance, and reporting).

Éléments clés

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

• Master’s or Doctorate in Neuroscience or any other related discipline;
• Experience related to MRI (Magnetic Resonance Imaging) and theoretical & practical knowledge of the subject are preferred;
• MRI-related targeting dosing is an asset;
• Good interpersonal and communication skills;
• Strong problem-solving skills.

Informations spécifiques au poste

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Annual bonus based on performance;
• Schedule: Monday to Friday, 8:00 am to 4:15 pm;
• Hybrid position – half on-site & half remote;
• Permanent position as of the hiring, full-time 37.5hrs per week.

Pourquoi Charles River ?

• We offer competitive benefits and advantages from day one to support your well-being;
• Paid development training;
• 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.

À propos de 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.

À propos de 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.

Ce que nous offrons

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.

Job Overview

As a Neuroscience Scientist for our Toxicology team located in Laval, you will be overseeing study conduct of preclinical efficacy and/or toxicology studies. Combined with neuroscience expertise and MRI‑guided dosing responsibilities, the role expands to include scientific leadership in CNS models, technical oversight of neuroimaging, and precision delivery into the brain or CNS structures. 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:

• Design and oversee with prospective and current clients MRI-guided targeting strategies for CNS delivery and support commercial groups in the preparation of statement of work;
• Perform MRI-guided dosing in collaboration with the surgeon team, ensure accurate placement to minimize off-target dose administration;
• Develop and optimize MRI protocols and targeting methodologies and contribute to innovation in CNS drug delivery techniques;
• Function as an independent Study Director in accordance with the applicable Good Laboratory Practice regulations (GLPs);
• Designs, writes, reviews and edits, as necessary, Study Plans, amendments and study schedules that define and schedule all study activities;
• Oversees and coordinates all aspects of study procedures, whether performed within the department or by service departments;
• Ensures that projects are performed according to Standard Operating Procedures and Good Laboratory Practice regulations and is aware of appropriate regulations, guidelines and guidances;
• Writes, reviews, and edits, as necessary, draft or final reports that document all study related procedures and results;
• Prompt verbal or written communication with Sponsors on study related business;
• Oversees and coordinates study conduct (MRI protocol and Study Plan development, technical guidance, and reporting).

Key Elements

Qualifications minimales

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

• Master’s or Doctorate in Neuroscience or any other related discipline;
• Experience related to MRI (Magnetic Resonance Imaging) and theoretical & practical knowledge of the subject are preferred;
• MRI-related targeting dosing is an asset;
• Good interpersonal and communication skills;
• Strong problem-solving skills.

Informations spécifiques au rôle

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Annual bonus based on performance;
• Schedule: Monday to Friday, 8:00 am to 4:15 pm;
• Hybrid position – half on-site & half remote;
• 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;
• Paid development training;
• 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.

À propos d’Apotex Inc.

Apotex est une entreprise mondiale dans le domaine de la santé établie au Canada. Nous améliorons l’accès quotidien à des médicaments et à des produits de santé abordables et novateurs pour des millions de personnes dans le monde, grâce à un large portefeuille de produits pharmaceutiques et de santé des consommateurs de marque, génériques, biosimilaires et novateurs. Basée à Toronto et disposant de bureaux régionaux dans le monde entier, notamment aux États-Unis, au Mexique et en Inde, Apotex est la plus grande société pharmaceutique du Canada et constitue un partenaire de choix dans le domaine de la santé pour les Amériques en matière de licences pharmaceutiques et d’acquisitions de produits.

Pour plus d’informations, rendez-vous sur le site : .

Résumé du poste

L’analyste en planification et analyse financières joue un rôle essentiel pour garantir des rapports précis et opportuns sur les performances de l’entreprise, ainsi que des prévisions financières complètes et fiables. Il s’agit d’un poste à forte visibilité, qui constitue une ressource clé pour le directeur de la planification et de l’analyse financières ainsi que pour les autres décideurs de haut niveau du secteur commercial.

Ce poste exige un grand souci du détail, de solides capacités d’analyse ainsi que d’excellentes compétences en communication orale et écrite.

Le candidat idéal possédera une solide expérience en planification et analyse financières (FP&A), ainsi qu’une expérience pratique de la gestion d’un modèle financier d’entreprise, du partenariat avec les unités fonctionnelles et de la création d’outils d’analyse commerciale pertinents.

Responsabilités

Responsabilités inhérentes au poste

• Effectuer une analyse mensuelle des écarts en comparant les résultats réels aux budgets et aux prévisions, et déterminer les principaux facteurs de performance
• Participer à l’élaboration des prévisions trimestrielles continues en collaborant avec les principaux partenaires commerciaux et en examinant les hypothèses actuelles
• Élaborer et maintenir des modèles financiers pour les prévisions et la budgétisation
• Animer les réunions mensuelles d’évaluation du service et fournir un soutien au besoin
• Préparer toutes les provisions des revenues et des calculs du brut au net, y compris les rabais des ventes, la rétrofacturation et les retours
• Superviser les comptes clients et les flux de trésorerie, et être le principal point de contact de l’équipe de recouvrement externe
• Déterminer les occasions d’amélioration de l’efficacité grâce à l’automatisation, aux améliorations des systèmes et aux processus évolutifs

Exigences

Exigences du poste

• Baccalauréat en finance, en comptabilité ou dans un domaine connexe et une désignation professionnelle (CPA, CFA, MBA)
• Trois années d’expérience en planification et analyse financières
• Maîtrise avancée d’Excel et de la modélisation financière
• Une expérience de travail avec SAP, les outils EPM (OneStream, Hyperion ou Anaplan) et les outils d’IA est préférable
• Solides compétences analytiques, souci du détail et capacité à prioriser dans un environnement dynamique
• Excellentes compétences en communication écrite et orale

Informations complémentaires

Chez Apotex, nous nous engageons à favoriser un environnement de travail accueillant et accessible, où tout le monde se sent valorisé, respecté et soutenu pour réussir.

Nous proposons des aménagements pour les candidats handicapés dans le cadre de leur processus de recrutement. Si vous êtes invité(e) à passer un entretien ou un examen, veuillez nous informer des mesures d’adaptation requises, le cas échéant.

Ce poste exige une connaissance approfondie de l’anglais car, faisant partie d’une équipe nationale bilingue travaillant ensemble à la gestion financière de l’entreprise à travers le Canada, l’employé doit être en mesure de communiquer avec ses collègues anglophones des autres provinces.

Chez Apotex, nous nous engageons à favoriser un environnement de travail accueillant et accessible, où tout le monde se sent valorisé, respecté et soutenu pour réussir.

Nous proposons des aménagements pour les candidats handicapés dans le cadre de leur processus de recrutement. Si vous êtes invité(e) à passer un entretien ou un examen, veuillez nous informer des mesures d’adaptation requises, le cas échéant.

Rémunération

La fourchette salariale pour ce poste se situe entre 72,284.85$ et 101,198.79$ CA par an. Le salaire final convenu peut varier en fonction de facteurs tels que les connaissances, les compétences et l'expérience liées au poste.

Nous sommes à la recherche de talents d'exception. Si vos qualifications diffèrent de celles énumérées ci-dessus, le champ d'application du travail et le salaire final convenu pourront être ajustés afin de refléter vos qualifications individuelles.

Le programme de rémunération globale d'Apotex va bien au-delà du salaire de base. Apotex propose des programmes de primes adaptés à votre poste au sein de l'organisation, vous permettant d'exceller grâce à notre philosophie de rémunération axée sur la performance. Grâce à des avantages sociaux complets, à un régime de retraite conçu pour vous aider à épargner pour l'avenir et à des opportunités d'apprentissage et de perfectionnement, nous offrons un ensemble complet favorisant votre développement tant sur le plan personnel que professionnel.

Processus de candidature

Apotex aura recours à l'intelligence artificielle pour le tri, la sélection et/ou l'évaluation de votre candidature pour ce poste.

Cette offre d'emploi concerne un poste actuellement disponible et vacant chez Apotex.