2887 offres d'emploi

Architecture d’entreprise - ERP - exemple Microsoft Dynamics

Employeur

9986782 CANADA INC.

Description du poste

Télétravail Montréal ou Québec avec 1 jour sur site Montréal ou Québec, Pour le poste permanent 4 semaines de congés par année, assurance après 3 mois.

Le ou la ressource conseiller en architecture d’entreprise contribuera à la réalisation de certains livrables de gouvernance en ressources informationnelles. Il contribuera à la transformation numérique de Retraite Québec et assurera la mise à jour de certains plans et stratégies.

Ainsi, il doit avoir œuvré dans le domaine de la fonction publique québécoise. Ces travaux incluent notamment les suivantes :

• Planifier et coordonner des travaux
• Réaliser des ateliers de collecte d’information
• Rédiger les livrables nécessaires à ses mandats et les supports visuels requis
• Soutenir l’équipe dans la réalisation des mandats stratégiques
• Conseiller son gestionnaire en matière de bonnes pratiques en RI

Le spécialiste devra produire le matériel requis pour présenter sommairement, clairement et dans un langage adapté, les dossiers qui lui sont confiés à toute partie prenante concernée.

Finalement, il devra appuyer les autres conseillers en architecture dans le cadre de production de livrables de gouvernance en RI.

Biens livrables :

• Diagnostic sur l’état de santé des actifs informationnels
• Stratégie et plan de modernisation des actifs informationnels
• Sommaire exécutif et autres livrables de gouvernances en lien avec les travaux de l’équipe d’architecture d’entreprise
• Produire des stratégies, l’état d’avancement ainsi que la reddition de comptes requises sur les dossiers d’arrimage avec l’écosystème gouvernemental.
• Présentations exécutives des dossiers
• Plans de communication aux hautes instances
• Veille et étalonnage sur les meilleures pratiques en AEStratégie en matière de main d’œuvres et plan de formations

Qualifications et compétences

Qualifications professionnelles

Cette offre d'emploi est soumise à une qualification professionnelle reconnue en dehors du réseau scolaire ou universitaire : (certificats, permis, cours, appartenance à un ordre ou une association professionnelle, etc.)

Formations

• Attestation d’études collégiales (AEC), Techniques de l'administration - Informatique
• Diplôme d’études collégiales (DEC), Techniques de l'informatique - Gestion de réseaux informatiques
• DEC-BAC, Techniques de l'administration - Conseil en assurances et en services financiers/ Administration des affaires
• Baccalauréat 1er cycle, Informatique - Systèmes informatiques et électroniques
• Maîtrise 2e cycle, Informatique - Technologie de l’information

Compétences

• Capacité à concevoir et à adapter de l’équipement ou des technologies
• Leadership
• Capacité de jugement et facilité à prendre des décisions

Langues

• Français parlé et écrit - Élevé
• Anglais parlé et écrit - Élevé

Conditions d’emploi

Horaire

Jour

Nombre d'heures

40 heures

Date de fin d'emploi

30 juin 2028

Expérience

5 à 10 ans

Durée d'emploi

Permanent

Travailleuses et travailleurs expérimentés

Cette offre d'emploi provient d'un employeur disposé à embaucher des travailleurs expérimentés. Pour plus d'information : Travailleurs expérimentés sur le marché du travail | Gouvernement du Québec (quebec.ca)

Description du poste

SUMMARY

We are seeking an experienced, organized, discreet, and versatile Housekeeper to oversee the upkeep and day-to-day management of a private residence located in Hampstead, Montreal.

The successful candidate will be responsible for maintaining a clean, well-presented, organized, and comfortable home environment. This individual will also occasionally prepare the evening meal, ready to be served or reheated, according to the family's needs.

Responsabilités clés

Housekeeping and Home Organization

• Maintain the overall cleanliness of occupied areas, including general housekeeping, dusting, and floor care.
• Perform deep cleaning as required, including bathrooms, showers, the oven, terrace, and balconies.
• Ensure the home remains clean, organized, welcoming, and well-maintained at all times.
• Make beds and change linens as needed.
• Organize storage areas, closets, and personal belongings.
• Monitor and rotate food items in the refrigerator and pantry.
• Store, organize, and rotate seasonal clothing.
• Care for furniture, delicate surfaces, and items requiring special attention.
• Ensure the residence remains functional, orderly, and well maintained.

Laundry and Wardrobe Care

• Sort, wash, fold, and iron clothing and household linens.
• Provide general care for garments and textile items.
• Perform minor clothing repairs and alterations as needed.
• Maintain closets and wardrobes in an organized and orderly manner.

Cooking and Meal Preparation

• Occasionally prepare the evening meal.
• Prepare simple, healthy, and well-balanced meals.
• Ensure meals are ready to be served or reheated according to established instructions.
• Maintain a clean, organized, and orderly kitchen following meal preparation.

Household Support and Logistics

• Provide daily care for three (3) dogs.
• Coordinate walks, grooming appointments, veterinary visits, and related pet care needs.
• Run household errands, including grocery shopping and replenishment of household supplies.
• Occasionally transport children to activities, appointments, and other engagements.
• Welcome contractors and service providers attending the residence.
• Maintain a professional and courteous presence with vendors and external service providers.
• Oversee service visits as required and communicate any relevant information to the family.
• Manage waste, recycling, and related household tasks.
• Report any issues requiring attention within the residence.

Qualifications et exigences

• Proven experience as a Housekeeper, Household Assistant, or in the maintenance of a private residence.
• Enjoys cooking and is comfortable preparing simple, healthy, family-style meals.
• Must be fluent in either English or French.
• Excellent organizational skills and strong attention to detail.
• Discretion, reliability, honesty, and professionalism.
• Ability to work independently and manage priorities effectively.
• Proactive, meticulous, versatile, and committed to maintaining high standards.
• Respect for confidentiality and the family environment.
• Positive attitude and strong adaptability.
• Valid driver's license required.

Informations supplémentaires

• Permanent full-time position.
• Schedule: Monday to Friday, 9:00 a.m. to 5:00 p.m. (flexibility required).
• Work location: Hampstead, Quebec.
• Competitive salary based on experience and qualifications.
• Residence accessible by public transportation.
• On-site parking available.
• Vehicle available for work-related duties.

Candidature

If you are an experienced Housekeeper with prior experience working in a private household, and you are organized, versatile, and detail-oriented, we would be pleased to receive your application. Qualified candidates are invited to submit their résumé to or apply online.

We thank all applicants for their interest; however, only those selected for an interview will be contacted.

Exigences

Proven experience as a Housekeeper, Household Assistant, or in the maintenance of a private residence. Enjoys cooking and is comfortable preparing simple, healthy, family-style meals. Must be fluent in either English or French. Excellent organizational skills and strong attention to detail. Discretion, reliability, honesty, and professionalism. Ability to work independently and manage priorities effectively. Proactive, meticulous, versatile, and committed to maintaining high standards. Respect for confidentiality and the family environment. Positive attitude and strong adaptability. Valid driver's license required.

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 poste

• 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

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

We are seeking an experienced Rally Product Support professional with 7-10 years of experience to join our team. This role requires a strong technical background in scripting, particularly Python, and experience working with REST APIs. The ideal candidate will be adept at integration workflow automation, data synchronization between Jira Cloud and Rally using Connectall, and possess strong problem-solving skills. This is a full-time contract position based in Montreal, requiring onsite presence three days a week, with relocation assistance available.

Responsabilités clés

• Automate and configure workflows and data synchronization jobs between Rally and Jira.
• Develop scripts to extract data from various IT systems (PPM+, ServiceNow) and generate reports.
• Ensure the uptime, performance, reliability, and scalability of the Rally product.
• Troubleshoot and debug issues related to integration between Rally and Jira.
• Collaborate with teams and stakeholders to onboard business squads and Fleets to Rally.

Qualifications requises

• Strong understanding of RESTful APIs and programmatic interaction.
• Experience in API integration between IT Systems.
• Proficiency in working with JSON and other data formats for API communication.
• Strong problem-solving and debugging skills.
• Ability to work independently and manage multiple tasks efficiently.
• Experience with Rally, Jira, and Connectall for data synchronization and workflow automation.
• Knowledge of Agile methodologies and experience working with Agile teams in Atlassian JIRA.

Qualifications préférées

• Knowledge of SDLC and DevOps.
• Knowledge of AI (Anthropic Claude and OpenAI).

Éducation

Education: Bachelors Degree

Présentation

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 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.

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: $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.

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 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 rôle

• 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!

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 across 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

SUMMARY

We are seeking an experienced, organized, discreet, and versatile Housekeeper to oversee the upkeep and day-to-day management of a private residence located in Hampstead, Montreal.

The successful candidate will be responsible for maintaining a clean, well-presented, organized, and comfortable home environment. This individual will also occasionally prepare the evening meal, ready to be served or reheated, according to the family's needs.

Responsabilités clés

Entretien ménager et organisation du domicile

• Maintain the overall cleanliness of occupied areas, including general housekeeping, dusting, and floor care.
• Perform deep cleaning as required, including bathrooms, showers, the oven, terrace, and balconies.
• Ensure the home remains clean, organized, welcoming, and well-maintained at all times.
• Make beds and change linens as needed.
• Organize storage areas, closets, and personal belongings.
• Monitor and rotate food items in the refrigerator and pantry.
• Store, organize, and rotate seasonal clothing.
• Care for furniture, delicate surfaces, and items requiring special attention.
• Ensure the residence remains functional, orderly, and well maintained.

Entretien du linge et garde-robe

• Sort, wash, fold, and iron clothing and household linens.
• Provide general care for garments and textile items.
• Perform minor clothing repairs and alterations as needed.
• Maintain closets and wardrobes in an organized and orderly manner.

Préparation des repas

• Occasionally prepare the evening meal.
• Prepare simple, healthy, and well-balanced meals.
• Ensure meals are ready to be served or reheated according to established instructions.
• Maintain a clean, organized, and orderly kitchen following meal preparation.

Soutien à la maison et logistique

• Provide daily care for three (3) dogs.
• Coordinate walks, grooming appointments, veterinary visits, and related pet care needs.
• Run household errands, including grocery shopping and replenishment of household supplies.
• Occasionally transport children to activities, appointments, and other engagements.
• Welcome contractors and service providers attending the residence.
• Maintain a professional and courteous presence with vendors and external service providers.
• Oversee service visits as required and communicate any relevant information to the family.
• Manage waste, recycling, and related household tasks.
• Report any issues requiring attention within the residence.

Qualifications et exigences

• Proven experience as a Housekeeper, Household Assistant, or in the maintenance of a private residence.
• Enjoys cooking and is comfortable preparing simple, healthy, family-style meals.
• Must be fluent in either English or French.
• Excellent organizational skills and strong attention to detail.
• Discretion, reliability, honesty, and professionalism.
• Ability to work independently and manage priorities effectively.
• Proactive, meticulous, versatile, and committed to maintaining high standards.
• Respect for confidentiality and the family environment.
• Positive attitude and strong adaptability.
• Valid driver's license required.

Informations supplémentaires

• Permanent full-time position.
• Schedule: Monday to Friday, 9:00 a.m. to 5:00 p.m. (flexibility required).
• Work location: Hampstead, Quebec.
• Competitive salary based on experience and qualifications.
• Residence accessible by public transportation.
• On-site parking available.
• Vehicle available for work-related duties.

Comment postuler

If you are an experienced Housekeeper with prior experience working in a private household, and you are organized, versatile, and detail-oriented, we would be pleased to receive your application. Qualified candidates are invited to submit their résumé to or apply online.

We thank all applicants for their interest; however, only those selected for an interview will be contacted.

Requirements

Proven experience as a Housekeeper, Household Assistant, or in the maintenance of a private residence. Enjoys cooking and is comfortable preparing simple, healthy, family-style meals. Must be fluent in either English or French. Excellent organizational skills and strong attention to detail. Discretion, reliability, honesty, and professionalism. Ability to work independently and manage priorities effectively. Proactive, meticulous, versatile, and committed to maintaining high standards. Respect for confidentiality and the family environment. Positive attitude and strong adaptability. Valid driver's license required.

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 an Animal Care Trainer for our Toxicology team at the Laval location, you will train technical staff and ensure that the training records are up to date and that the techniques taught are done in a way that respects established processes.

In this role, primary responsibilities include:

• Train animal room cleaning and restraint methods;
• Train on the data recording such as body weight, food consumption and clinical signs in order to meet quality and competence standards;
• Evaluate the employee's level of understanding in relation to the training received;
• 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;
• Ensure the follow-up of the various changes brought to the procedures and the methods of work and participate in process improvement efforts;
• Ensure good communication with the supervisors of the different departments during and after completion of the employees’ training.

Exigences

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

• High School diploma;
• At least 2 to 3 years’ experience in a research center as an Animal Care Clerk/Animal Care Attendant;
• Be a reference, an example and a leader for Animal Welfare, Health and Safety, Quality and attendance;
• Good observation skills;
• Ability to inspire trust and confidence through strong interpersonal skills and effective collaboration;
• 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 poste

Role Specific Information:

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Salary: Starting at 22$/hrs;
• Annual bonus based on performance;
• Schedule: Monday to Friday, daytime;
• Permanent position as of the hiring, full-time 37.5hrs per week.

Ce que nous offrons

Why Charles River ?

• We offer competitive benefits and advantages from day one to support your well-being;
• Employee and family assistance program;
• Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
• Access to a doctor and various health professionals (telemedicine);
• 3 weeks’ Vacation & 5 Personal day policy;
• Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

À propos de Safety Assessment

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.

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 Care Clerk (Toxicology)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.

Description du poste

As an Animal Care Clerk for our Toxicology team located 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:

• Ensure the cleanliness of the living environment of the animals according to the highest standards of welfare in the industry (clean the animal rooms and the cages);
• Assist the Animal Health Technicians in their daily tasks;
• Handle animals;
• Participate in the physical/social activities of the animals.

Éléments clés

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

• Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
• You are able to follow precises instructions (procedures);
• You like animals.

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: $19/hrs;
• Premiums: Evening ($2.50), Weekend ($2.75), Overtime (Time and a half), Holidays (Double time);
• Annual bonus based on performance plan;
• Schedule: Flexible schedule, you must be available days, evening, and weekends (1/2). Depending on the needs, you may have to do overtime night, and holidays;
• Permanent position as of the hiring, 37.5hrs per week;
• Career progression: If you are interested in progressing and learning more, we can train you to become an Animal Health Technician! Of course, that comes with a pay rise.

Pourquoi Charles River ?

• Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
• Paid development training;
• Employee and family assistance program;
• Access to a doctor and various health professionals (telemedicine);
• Guaranteed hours because the research field is in high demand;
• 3 weeks’ Vacation & 5 Personal days;
• 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 120 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 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

Le responsable de la planification et de l'analyse financières joue un rôle essentiel pour garantir des rapports précis et opportuns sur le rendement commercial, 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 inhérentes à l’emploi

• Diriger l’élaboration, la consolidation et l’analyse des budgets annuels, des prévisions trimestrielles pour s’adapter à l’évolution de la conjoncture et des plans à long terme.
• Collaborer avec les équipes fonctionnelles pour garantir des données précises et opportunes, offrant une visibilité en temps réel sur le rendement financier.
• Superviser tous les aspects de la comptabilisation et du contrôle des revenus de la division, y compris les régularisations brutes et nettes, la gestion des comptes clients et les prévisions de trésorerie.
• Superviser le rapprochement des résultats financiers réels avec les budgets et les prévisions.
• Préparer des rapports financiers et des analyses complets et précis.
• Assurer la liaison entre l’équipe financière et les autres services internes. Faciliter la communication, partager les informations et assurer la circulation précise des informations financières au sein de l’organisation.
• Gérer et développer des rapports financiers qui harmonisent et simplifient les revues d’activité mensuelles, la planification annuelle et les processus de prévision.
• Fournir un soutien en matière d'analyse concurrentielle, notamment en ce qui concerne la tarification optimale des produits et les analyses internes des gains et des pertes.
• Mettre en œuvre des stratégies de gestion et d’optimisation des dépenses d’exploitation, en veillant à leur alignement avec les objectifs financiers et la vision à long terme de l’entreprise.

Exigences

• Baccalauréat en finance, en comptabilité ou dans un domaine connexe et une désignation professionnelle (CPA, CFA, MBA)
• Minimum de 5 ans d’expérience en planification et analyse financières.
• Maîtrise avancée d’Excel et de la modélisation financière; capacité à construire et à maintenir de manière autonome des modèles complexes.
• 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.

Ce que nous offrons

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.

La fourchette salariale pour ce poste se situe entre 95 594,40 $ et 133 832,16 $ 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.

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.

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.

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

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.

Responsabilités principales

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

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

Informations propres au rôle

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.

Pourquoi Charles River ?

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.

À propos de Safety Assessment

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.

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

SUMMARY

We are seeking an experienced, organized, discreet, and versatile Housekeeper to oversee the upkeep and day-to-day management of a private residence located in Hampstead, Montreal.

The successful candidate will be responsible for maintaining a clean, well-presented, organized, and comfortable home environment. This individual will also occasionally prepare the evening meal, ready to be served or reheated, according to the family's needs.

Responsabilités clés

Entretien ménager et organisation de la maison

• Maintain the overall cleanliness of occupied areas, including general housekeeping, dusting, and floor care.
• Perform deep cleaning as required, including bathrooms, showers, the oven, terrace, and balconies.
• Ensure the home remains clean, organized, welcoming, and well-maintained at all times.
• Make beds and change linens as needed.
• Organize storage areas, closets, and personal belongings.
• Monitor and rotate food items in the refrigerator and pantry.
• Store, organize, and rotate seasonal clothing.
• Care for furniture, delicate surfaces, and items requiring special attention.
• Ensure the residence remains functional, orderly, and well maintained.

Entretien du linge et de la garde-robe

• Sort, wash, fold, and iron clothing and household linens.
• Provide general care for garments and textile items.
• Perform minor clothing repairs and alterations as needed.
• Maintain closets and wardrobes in an organized and orderly manner.

Préparation des repas et cuisine

• Occasionally prepare the evening meal.
• Prepare simple, healthy, and well-balanced meals.
• Ensure meals are ready to be served or reheated according to established instructions.
• Maintain a clean, organized, and orderly kitchen following meal preparation.

Soutien à la maison et logistique

• Provide daily care for three (3) dogs.
• Coordinate walks, grooming appointments, veterinary visits, and related pet care needs.
• Run household errands, including grocery shopping and replenishment of household supplies.
• Occasionally transport children to activities, appointments, and other engagements.
• Welcome contractors and service providers attending the residence.
• Maintain a professional and courteous presence with vendors and external service providers.
• Oversee service visits as required and communicate any relevant information to the family.
• Manage waste, recycling, and related household tasks.
• Report any issues requiring attention within the residence.

Qualifications et exigences

• Proven experience as a Housekeeper, Household Assistant, or in the maintenance of a private residence.
• Enjoys cooking and is comfortable preparing simple, healthy, family-style meals.
• Must be fluent in either English or French.
• Excellent organizational skills and strong attention to detail.
• Discretion, reliability, honesty, and professionalism.
• Ability to work independently and manage priorities effectively.
• Proactive, meticulous, versatile, and committed to maintaining high standards.
• Respect for confidentiality and the family environment.
• Positive attitude and strong adaptability.
• Valid driver's license required.

Informations supplémentaires

• Permanent full-time position.
• Schedule: Monday to Friday, 9:00 a.m. to 5:00 p.m. (flexibility required).
• Work location: Hampstead, Quebec.
• Competitive salary based on experience and qualifications.
• Residence accessible by public transportation.
• On-site parking available.
• Vehicle available for work-related duties.

Comment postuler

If you are an experienced Housekeeper with prior experience working in a private household, and you are organized, versatile, and detail-oriented, we would be pleased to receive your application. Qualified candidates are invited to submit their résumé to or apply online.

We thank all applicants for their interest; however, only those selected for an interview will be contacted.

Manager Regulatory Affairs Operations

Description du poste

The Manager, Regulatory Affairs Operations provides technical and operational leadership, and strategic partnership for regulatory publishing and submission activities to global Health Authorities (e.g., FDA, Health Canada, and international agencies). This role is accountable for ensuring high-quality, compliant, and timely regulatory submissions across the product lifecycle, while also driving process optimization, technical standards, and capability development within Regulatory Affairs Operations.

In addition to hands-on oversight of complex submissions, the Manager plays a key role, providing technical guidance and upskilling to cross-functional partners and vendors, and shaping the globalization and modernization of regulatory publishing processes in alignment with evolving Health Authority expectations and internal digital strategies.

Fonctions essentielles

Regulatory Submission & Technical Oversight

• Provides technical oversight and quality accountability for IND, NDA, BLA, and DMF original and lifecycle submissions in eCTD format, ensuring compliance with global Health Authority requirements and internal standards.
• Oversees and reviews critical publishing components (e.g., eCTD structure, metadata, hyperlinks, lifecycle management, validation results) to ensure submission readiness and inspection defensibility.
• Serves as a technical escalation point for complex publishing issues, including direct interaction with Health Authorities to assess submission troubleshooting and issue resolution.
• Ensures consistent application of regulatory publishing standards across programs, products, and regions.

Process Ownership & Modernization

• Contributes to the development, implementation, and continuous improvement of regulatory publishing processes, SOPs, work instructions, and technical standards.
• Provides subject matter leadership for the globalization of publishing practices, supporting harmonized approaches across regions and affiliates.
• Actively supports modernization and digital enablement initiatives, including adoption, validation, and optimization of publishing tools, systems, and technologies.
• Participates in system validation, upgrades, and implementation efforts, ensuring regulatory and inspection readiness.

Training, Capability Building & Cross-Functional Enablement

• Under the direction of Assoc. Dir, supports the development and delivers role-based training for Regulatory Affairs Operations staff on publishing standards, tools, lifecycle management, and Health Authority expectations.
• Responsible to develop and deliver training for cross-functional SMEs (e.g., Regulatory Affairs, CMC, Clinical, Biostats, Labeling) on technical data and document readiness regulatory requirements to support high-quality submissions.
• Acts as a technical mentor and coach to the Regulatory Publishing team, supporting skill development and consistency in publishing practices.

Leadership & Operational Support

• Supports the functional management in workload planning, prioritization, and resource allocation for regulatory submissions.
• Serves as a liaison to global counterparts in publishing and operations to drive organizational effectiveness.
• Provides guidance to internal staff and external vendors/contractors involved in publishing activities.
• May participate in submission task forces, kickoff meetings, inspections, audits, and special projects as a Regulatory Operations representative.
• Contributes to departmental metrics, compliance monitoring, and inspection preparedness activities.

Exigences

• Accredited bachelor's degree
• 5+ years of experience in Regulatory Affairs, Regulatory Operations, or R&D Submission Support within the pharmaceutical industry
• 5+ years of direct, hands-on experience with eCTD publishing software across multiple regions, including the US, EU, Canada, and Rest of World (ROW)
• Expert-level proficiency with MS Office Suite and Adobe Acrobat, including regulatory publishing tools and plugins such as ISI Toolbox and SmartDesk
• Demonstrated proficiency with document management systems (EDMS), eCTD validators, and XML/SPLs
• Hands-on experience submitting SPLs, datasets (SEND, ADAM), and related regulatory submission components
• Proven ability to manage shifting priorities and successfully complete multiple tasks with overlapping deadlines
• Strong attention to detail and excellent organizational skills

Qualifications préférées

• Project/Submission Readiness Management skills
• Cross Functional Team participation
• Experience using Docubridge submission publishing system
• Experience with Veeva systems (i.e. eTMF, PromoMats, RIM)
• Strong Preference to be based in Deerfield, IL Office

Voyage

• Willingness/Ability to travel up to 10% domestically. International travel may be required.

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 propres 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 ?

Why Charles River ?

• We offer competitive benefits and advantages from day one to support your well-being;
• Employee and family assistance program;
• Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
• Access to a doctor and various health professionals (telemedicine);
• 3 weeks’ Vacation & 5 Personal day policy;
• Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

À propos de Safety Assessment

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.

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

Nous recherchons quelqu’un pour s’occuper de Mamey pendant un voyage en famille de 16 jours. Mamey est un bouledogue français, un très bon chien. Il est généralement bien avec les enfants et les autres animaux.

Il sort toujours pour faire ses besoins : 4 à 5 fois par jour, toutes les 4 à 5 heures (7 h 30, 13 h, 17 h, 21 h).

La période concernée va du mardi 18 janvier au 5 juillet.

Tâches

• S’occuper de Mamey pendant la période indiquée
• Le faire sortir pour faire ses besoins 4 à 5 fois par jour (toutes les 4 à 5 heures : 7 h 30, 13 h, 17 h, 21 h)

Rémunération

Je propose un taux de rémunération quotidien de 15 $ pour ce poste de pet-sitting.

Profil recherché

Cette opportunité est idéale pour les amoureux des animaux à La Prairie qui souhaitent passer du temps de qualité avec les chiens et gagner un peu d’argent supplémentaire.

Si vous êtes intéressé(e) par ce poste de garde et que vous pensez être la bonne personne pour prendre soin de mes chiens, n’hésitez pas à me contacter. J’ai hâte d’avoir de vos nouvelles et de trouver quelqu’un qui traitera mes animaux avec l’amour et les soins qu’ils méritent.

Veuillez consulter la page pour voir les détails complets et postuler. Il y a beaucoup d’emplois parmi lesquels choisir !

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 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 minimales

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 propres 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 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!

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.

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 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.

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: $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.

Pourquoi Charles River ?

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.

À propos de Safety Assessment

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.

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

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 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 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!

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 across 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.

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!

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.

Neuroscience Research Scientist – Toxicology (Laval)

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.

As a Neuroscience Research 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).

Éléments clés

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

• Master’s or Doctorate in Neuroscience or any other related discipline;
• At least 3 years of relevant experience in a Scientist position;
• 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.

Information spécifique 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);
• 4 weeks’ Vacation & 10 Personal day policy;
• Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

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.

Aperçu du poste

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).

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.

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.