3175 offres d'emploi

De nouveaux défis, c’est juste ici!

• Nombre d’emplois offerts : 1
• Statut de l’emploi : emploi régulier
• Mode d’organisation du travail : travail en mode hybride
• Lieu de travail : Québec ou Laval

Le lieu de travail sera déterminé en fonction de la personne sélectionnée.

Votre contribution à la mission de Revenu Québec

Le Service de la sécurité de l’information et du soutien au traitement massif de Revenu Québec, c’est une équipe de plus de 22 personnes qui contribuent chaque jour à assurer le pilotage, le développement et l’amélioration des outils informatiques essentiels aux opérations de la Direction générale du recouvrement, en plus de jouer un rôle de soutien.

En évoluant au sein de cette équipe, vous collaborerez avec vos collègues en vue de relever des défis stimulants, comme contribuer à l’élaboration et à l’intégration d’initiatives fondées sur l’intelligence artificielle (IA). L’innovation et la collaboration sont des principes fondamentaux qui guideront votre travail au quotidien.

Votre quotidien à Revenu Québec

En tant que conseillère ou conseiller en architecture de solutions fondées sur l’IA, vous devrez

• établir l’architecture de solutions fondées sur l’IA, en plus de définir la vision et les principes d’intégration sur lesquels elles reposent;
• vous assurer de la sécurité, de la performance et de l’évolution des solutions;
• concevoir et encadrer l’architecture des solutions fondées sur l’IA, y compris les flux de données, les modèles et leur intégration dans les systèmes existants;
• contribuer à la sélection des technologies, des plateformes et des outils appropriés;
• accompagner les équipes dans la conception et le déploiement des solutions;
• exercer le rôle de personne-ressource et de vigie en matière d’architecture fondée sur l’IA et d’évolution technologique.

En prime, vous aurez l’occasion de vous épanouir professionnellement grâce au soutien d’une équipe qui aura à cœur votre réussite et votre avancement.

Les prérequis

Pour vous joindre à notre équipe, vous devez

• détenir
  • soit un diplôme universitaire de premier cycle (baccalauréat) ou l’équivalent dans l’un des domaines suivants ou dans tout autre domaine jugé pertinent :
    • informatique,
    • IA,
    • science des données;
  • soit un diplôme universitaire de premier cycle (baccalauréat) dans tout autre domaine et avoir minimalement une année d’expérience jugée pertinente;
• avoir de l’expérience dans le domaine de l’architecture informatique.

Par ailleurs, les éléments suivants pourraient être considérés comme des atouts :

• avoir de l’expérience en IA ou en transformation numérique;
• avoir de l’expérience dans la conception ou la mise en place d’architectures de solutions fondées sur l’IA.

Informations complémentaires

Vous devez avoir le statut de citoyen canadien ou celui de résident permanent, ou encore être titulaire d’un permis de travail valide au Canada.

Si vous avez obtenu votre diplôme à l’extérieur du Canada, vous devez joindre une copie de l’évaluation comparative d’études délivrée par le ministère de l’Immigration, de la Francisation et de l’Intégration à votre dossier en ligne. Notez que, si vous ne fournissez pas ce document au moment de compléter votre dossier, vous ne pourrez pas transmettre votre candidature.

Vos qualités professionnelles

Ce poste vous plaira si vous

• faites preuve d’une vision stratégique développée et d’un sens éthique;
• démontrez un esprit de collaboration et êtes capable de travailler efficacement dans un environnement interdisciplinaire;
• possédez des aptitudes marquées en communication.

Des conditions de travail avantageuses, c’est juste ici!

• Minimum de quatre semaines de vacances après la première année
• Subvention pour la pratique d’activités physiques
• Horaire flexible et différents types de congés offerts

Quelques précisions

Nous recrutons aux endroits suivants :

• Québec (3800, rue de Marly)
• Laval (5, Place-Laval)

Les modalités d’inscription

• Nous vous invitons à consulter les étapes liées au processus de recrutement via Espresso-jobs
• Vous devez fournir toutes les informations demandées dans le formulaire électronique, même si elles sont déjà inscrites dans votre curriculum vitæ. Si vous apportez des modifications à celui-ci après la période d’inscription, elles ne seront pas considérées.

Vous avez des questions?

Nous sommes là pour répondre à toutes vos questions. Contactez-nous par téléphone au 418 652-6601 (région de Québec), au 514 228-3139 (région de Montréal) ou au 1 855 824-0337 (sans frais).

Programme d’accès à l’égalité en emploi

Revenu Québec applique un programme d’accès à l’égalité en emploi et invite les femmes, les personnes handicapées, les autochtones, les minorités visibles et les minorités ethniques à présenter leur candidature. Des mesures d’adaptation peuvent être offertes aux personnes handicapées en fonction de leurs besoins.

Votre quotidien à Revenu Québec

En tant qu’administratrice ou administrateur de plateforme ServiceNow, vous devrez

• effectuer le suivi quotidien de la plateforme, optimiser les infrastructures, maintenir les configurations et mettre en place des mécanismes permettant de suivre l’utilisation et la performance;
• configurer la plateforme, les découvertes et les intégrations ainsi qu’appliquer les règles de sécurité selon les standards et les procédures définis, tout en veillant à sa performance et à sa stabilité;
• collaborer avec les équipes de développement pour renforcer la sécurité, corriger les anomalies, faire évoluer la plateforme et réaliser les graduations dans les instances de ServiceNow;
• analyser et évaluer de nouvelles versions d’applications disponibles sur le marché et coordonner le déploiement de celles-ci.

En tant qu’analyste CMDB, vous devrez

• définir et documenter les éléments de configuration et leurs attributs, tout en assurant une gestion rigoureuse, cohérente et conforme aux bonnes pratiques en ITSM ;
• analyser les données actuelles de la CMDB, corriger les données erronées, aider les responsables de services à effectuer la maintenance ainsi que participer aux travaux liés aux mises à niveau et aux correctifs de la plateforme;
• réaliser des analyses régulières afin d’identifier des possibilités d’amélioration et mettre en œuvre des stratégies d’optimisation des inventaires informatiques, par exemple l’activation de la santé de la CMDB ;
• participer aux activités d’audit et de conformité pour garantir la conformité de la CMDB.

En tant que configuratrice ou configurateur de plateforme ServiceNow, vous devrez

• analyser les besoins fonctionnels ainsi que concevoir et documenter des solutions de configuration basées sur les bonnes pratiques de ServiceNow;
• configurer les applications et les modules de la plateforme, y compris notamment les formulaires, les flux de travail et les interfaces utilisateurs;
• participer aux travaux de mises à niveau et prendre en charge la résolution d’incidents liés aux configurations;
• assurer la qualité et la fiabilité des solutions configurées, tout en veillant à l’évolution continue de la plateforme ServiceNow.

En prime, vous aurez l’occasion de vous épanouir professionnellement grâce au soutien d’une équipe qui aura à cœur votre réussite et votre avancement.

Les prérequis

Pour vous joindre à notre équipe, vous devez

• détenir
  • soit un diplôme universitaire de premier cycle (baccalauréat) ou l’équivalent dans l’un des domaines suivants ou dans tout autre domaine jugé pertinent :

• • • informatique,
    • génie informatique,
    • génie logiciel,
    • administration (technologies de l’information);
  • soit un diplôme universitaire de premier cycle (baccalauréat) dans tout autre domaine et avoir minimalement une année d’expérience jugée pertinente;
  • détenir de l’expérience en lien avec la plateforme ServiceNow.

L’élément suivant pourrait être considéré comme un atout : avoir de l’expérience en lien avec la CMDB, la ITSM, le module ITOM et la gestion des actifs informatiques (ITAM).

Informations complémentaires

Vous devez avoir le statut de citoyen canadien ou celui de résident permanent, ou encore être titulaire d’un permis de travail valide au Canada.

Si vous avez obtenu votre diplôme à l’extérieur du Canada, vous devez joindre une copie de l’évaluation comparative d’études délivrée par le ministère de l’Immigration, de la Francisation et de l’Intégration à votre dossier en ligne. Notez que, si vous ne fournissez pas ce document au moment de compléter votre dossier, vous ne pourrez pas transmettre votre candidature.

Vos qualités professionnelles

Ce poste vous plaira si vous 

• faites preuve de créativité, d’initiative et d’innovation;
• démontrer une grande autonomie et un sens élevé des responsabilités;
• faites preuve de rigueur et d’un bon sens de l’organisation.

Des conditions de travail avantageuses, c’est juste ici!

• Minimum de quatre semaines de vacances après la première année
• Subvention pour la pratique d’activités physiques
• Horaire flexible et différents types de congés offerts
• Sécurité et stabilité en emploi
• Et bien plus encore!

Salaire

Le salaire sera déterminé à la suite d’une analyse de vos expériences de travail pertinentes et de votre formation. Il est donc important d’inscrire toutes ces informations dans votre dossier en ligne et votre curriculum vitæ.

Les modalités d’inscription

• Nous vous invitons à consulter les étapes liées au processus de recrutement via Espresso-jobs
• Vous devez fournir toutes les informations demandées dans le formulaire électronique, même si elles sont déjà inscrites dans votre curriculum vitæ. Si vous apportez des modifications à celui-ci après la période d’inscription, elles ne seront pas considérées.

Vous avez des questions?

Nous sommes là pour répondre à toutes vos questions. Contactez nous par téléphone au 418 652-6601 (région de Québec), au 514 228-3139 (région de Montréal) ou au 1 855 824-0337 (sans frais).

Programme d’accès à l’égalité en emploi

Revenu Québec applique un programme d’accès à l’égalité en emploi et invite les femmes, les personnes handicapées, les autochtones, les minorités visibles et les minorités ethniques à présenter leur candidature. Des mesures d’adaptation peuvent être offertes aux personnes handicapées en fonction de leurs besoins.

Numéro de l'offre
551E-26000147

Lieu de travail
Canada /
- 03-Capitale-Nationale
- 13-Laval

Statut d'emploi
Régulier

De nouveaux défis, c’est juste ici!

• Nombre d’emplois offerts : 1
• Statut de l’emploi : emploi régulier
• Mode d’organisation du travail : travail en mode hybride
• Lieu de travail : Québec ou Laval

Le lieu de travail sera déterminé en fonction de chaque personne sélectionnée.

Votre contribution à la mission de Revenu Québec

Le Service de la sécurité de l’information et du soutien au traitement massif de Revenu Québec, c’est une équipe de plus de 22 personnes qui contribuent chaque jour à assurer le pilotage, le développement et l’amélioration des outils informatiques essentiels aux opérations de la Direction générale du recouvrement, en plus de jouer un rôle de soutien.

En évoluant au sein de cette équipe, vous collaborerez avec vos collègues en vue de relever des défis stimulants, comme contribuer à l’élaboration et à l’intégration d’initiatives fondées sur l’intelligence artificielle (IA). L’innovation et la collaboration sont des principes fondamentaux qui guideront votre travail au quotidien.

Votre quotidien à Revenu Québec

En tant que conseillère ou conseiller en IA, vous devrez

• analyser les besoins d’affaires et identifier les possibilités d’intégration de l’IA, en tenant compte des enjeux organisationnels;
• évaluer les répercussions possibles, les bénéfices potentiels et les risques en lien avec les initiatives fondées sur l’IA afin d’orienter la prise de décisions;
• collaborer avec des équipes multidisciplinaires pour vous assurer d’un alignement entre les besoins, les solutions et les priorités organisationnelles;
• contribuer à la mise en œuvre, au déploiement et à l’évolution de solutions liées à l’IA, dans une perspective d’amélioration continue;
• participer à la collecte, à l’analyse et à la valorisation de données en vue de l’optimisation de systèmes et de processus;
• définir des orientations stratégiques et technologiques en lien avec l’intégration de stratégies fondées sur l’IA.

En prime, vous aurez l’occasion de vous épanouir professionnellement grâce au soutien d’une équipe qui aura à cœur votre réussite et votre avancement.

Les prérequis

Pour vous joindre à notre équipe, vous devez

• détenir
  • soit un diplôme universitaire de premier cycle (baccalauréat) ou l’équivalent dans l’un des domaines suivants ou dans tout autre domaine jugé pertinent :
    • informatique,
    • IA,
    • science des données ou analytique,
    • administration ou administration des affaires;
  • soit un diplôme universitaire de premier cycle (baccalauréat) dans tout autre domaine et avoir minimalement une année d’expérience jugée pertinente;
• avoir de l’expérience en IA ou en transformation numérique.

Par ailleurs, avoir de l’expérience dans l’intégration ou le déploiement de solutions liées à l’IA pourrait être considéré comme un atout.

Informations complémentaires

Vous devez avoir le statut de citoyen canadien ou celui de résident permanent, ou encore être titulaire d’un permis de travail valide au Canada.

Si vous avez obtenu votre diplôme à l’extérieur du Canada, vous devez joindre une copie de l’évaluation comparative d’études délivrée par le ministère de l’Immigration, de la Francisation et de l’Intégration à votre dossier en ligne. Notez que, si vous ne fournissez pas ce document au moment de compléter votre dossier, vous ne pourrez pas transmettre votre candidature.

Vos qualités professionnelles

Ce poste vous plaira si vous

• démontrez des aptitudes marquées en communication et en vulgarisation;
• faites preuve d’un bon sens de l’autonomie et de l’organisation, et savez gérer les priorités;
• avez une grande facilité à travailler en équipe;
• accordez une grande importance à la performance et à l’atteinte des résultats.

Des conditions de travail avantageuses, c’est juste ici!

• Minimum de quatre semaines de vacances après la première année
• Subvention pour la pratique d’activités physiques
• Horaire flexible et différents types de congés offerts

Quelques précisions

Nous recrutons aux endroits suivants :

• Québec (3800, rue de Marly)
• Laval (5, Place-Laval)

Les modalités d’inscription

• Nous vous invitons à consulter les étapes liées au processus de recrutement, via Espresso-jobs
• Vous devez fournir toutes les informations demandées dans le formulaire électronique, même si elles sont déjà inscrites dans votre curriculum vitæ. Si vous apportez des modifications à celui-ci après la période d’inscription, elles ne seront pas considérées.

Vous avez des questions?

Nous sommes là pour répondre à toutes vos questions. Contactez-nous par téléphone au 418 652-6601 (région de Québec), au 514 228-3139 (région de Montréal) ou au 1 855 824-0337 (sans frais).

Programme d’accès à l’égalité en emploi

Revenu Québec applique un programme d’accès à l’égalité en emploi et invite les femmes, les personnes handicapées, les autochtones, les minorités visibles et les minorités ethniques à présenter leur candidature. Des mesures d’adaptation peuvent être offertes aux personnes handicapées en fonction de leurs besoins.

CE QUE LE CÉGEP VOUS OFFRE

À quelques pas du métro Du Collège, le cégep de Saint-Laurent est un milieu engagé et dynamique. Il dispose d’un grand campus vert où plus de 700 membres du personnel contribuent à la réussite de nos étudiants et étudiantes.

Nous sommes fiers de participer au programme d’accès à l’égalité en emploi, afin de créer des opportunités pour les femmes, les minorités ethniques et visibles, les personnes autochtones et les personnes en situation de handicap. Ensemble, nous pouvons continuer à bâtir un environnement inclusif et diversifié où chacun a sa place!

• 20 jours de vacances
• 13 jours fériés
• 7 jours de congé de maladie
• Assurances collectives
• Régime de retraite RREGOP
• Congés spéciaux (mariage, déménagement)
• Programme de perfectionnement et de formation
• Horaire flexible, conciliation travail et vie personnelle, CPE sur le campus
• Opus & Cie : tarif avantageux pour le transport en commun
• Accès à la bibliothèque et aux installations sportives (gym, piscine, aréna)

* Selon les dispositions de la convention collective

LA MISSION QUI VOUS ATTEND

L’emploi d’analystes spécialisés en informatique comporte plus spécifiquement la coordination, la gestion de projets, et la supervision des activités d’analyse, de mise en œuvre, d’évolution, d’implantation, de soutien opérationnel de projets concernant les ressources informationnelles et touchant plusieurs secteurs du Collège.

Nous recherchons une personne passionnée par le développement et l’automatisation afin de contribuer à l’évolution des processus de gestion des identités et des accès du Collège. Vous développerez des solutions efficaces et sécuritaires en collaboration avec différentes équipes afin d’assurer la fiabilité et l’évolution des mécanismes de gestion des accès.

Vous avez envie d’un poste rempli de sens et de défis? Rejoignez notre équipe!
Quelques attributions caractéristiques du poste :

Programmation et traitement de données (70 % de la tâche)

Assurer la continuité et l’évolution d’une architecture logicielle Python complexe composées d’une vingtaine de modules et d’une base de code de grande envergure ; Exploiter et traiter l’information de base de données complexes dans un processus automatisé de gestion des identités et des accès pour tous les usagers du Cégep ;Mettre en place des mécanismes d’intégration entre différents systèmes (AD, Azure AD, sites web, etc.)

Sécurité de l’information (30 % de la tâche)

Participer aux processus de gouvernance des identités et des accès ; Participer à la gestion des incidents de sécurité liés aux accès et aux données. Contribuer à la mise en œuvre de contrôles de sécurité dans un environnement infonuagique hybride (Microsoft 365) ;
Au besoin, accomplir toute autre tâche connexe.

LES ATOUTS QU’ON RECHERCHE

Qualifications requises

Diplôme universitaire terminal de premier cycle dans un champ de spécialisation approprié, notamment en informatique, génie logiciel ;Certification de spécialisation délivrée par une autorité compétente et reconnue notamment dans le domaine des ressources informationnelles (ex. : Microsoft Azure Fundamentals, Microsoft Information Security Administrator) ;Minimum de trois années d’expérience pertinente ;

Autres exigences :

Compétences recherchées :

• Excellente maîtrise de Python, SQL et des outils de gestion de version (Git);
• Bonne compréhension des environnements Microsoft 365 (accès conditionnel, DLP, étiquettes de sensibilité);
• Connaissance d’Active Directory et Azure AD;
• Capacité à évoluer dans des environnements complexes et interconnectés.

Qualités personnelles:

• Autonomie, esprit d’analyse et débrouillardise;
• Structuré et rigoureux dans ses développements logiciels (documentation de code, tests, journaux et validation);
• Sens du service et bonnes habiletés relationnelles.

Envoyez votre CV via Espresso-jobs.

Description du poste

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Exigences

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Informations supplémentaires

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Description du poste

VTRAC Consulting Corporation

Intelligent Resources

Location: Montreal, QC (Hybrid Quebec)

Type: Contract / Consulting

Term: 3-6 months

Le poste

Looking for a motivated and proactive IT Project Coordinator to support the successful delivery of digital transformation and customer engagement projects. This is an excellent opportunity for an early-career professional who has experience supporting technology projects and is eager to learn, take ownership, and grow within a consulting environment.

Responsabilités

• Coordinate project activities across multiple stakeholders and teams
• Support the planning, execution, and monitoring of digital and technology projects
• Facilitate project meetings, document decisions, action items, and follow-ups
• Assist with requirements gathering and documentation
• Support project scoping and solution design activities
• Maintain project plans, schedules, risks, issues, and status reports
• Prepare project documentation, specifications, and client deliverables
• Coordinate testing activities, test scenarios, and defect tracking
• Track project tasks and ensure timely completion of deliverables
• Support deployment planning and go-live readiness activities
• Assist with change management and user adoption initiatives
• Work closely with architects, consultants, and client stakeholders to ensure smooth project execution
• Utilize collaboration and project management tools including Microsoft 365, Teams, Jira, and related platforms

Qualifications

• 1–3 years of experience in Project Coordination, Project Administration, Business Analysis, Customer Success, Digital Marketing Technology, CRM, or a related field
• Experience supporting IT, CRM, Digital Marketing, SaaS, Martech, or customer experience projects is preferable
• Strong organizational and documentation skills
• Ability to manage multiple priorities and follow through on commitments
• Excellent communication and stakeholder management skills
• Comfortable working with both business and technical teams
• Experience with Microsoft Office 365, Teams, Jira, and project tracking tools
• Self-starter with a proactive attitude and strong attention to detail
• Ability to learn quickly and thrive in a fast-paced consulting environment

Atouts (Nice to Have)

• Exposure to CRM, Marketing Automation, Customer Data Platforms (CDP), Analytics, or Digital Experience platforms
• Experience working in a consulting or client-facing environment
• Knowledge of Agile or traditional project delivery methodologies

Exigences linguistiques

• Bilingual, professional French ( A MUST), and English communication skills
• Comfortable collaborating with French-speaking team members and clients
• Quebec French is not mandatory; strong business-level French is acceptable

Ce que la réussite implique

In the first 90 days, you will:

• Quickly onboard into client projects
• Build strong working relationships with architects and consultants
• Take ownership of project coordination activities
• Improve project organization and communication
• Successfully offload administrative and coordination tasks from senior technical resources

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.

Minimum qualifications

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 sur le 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: $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!

À propos

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

About Safety Assessment

Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

About Charles River

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Ce que nous offrons

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Technicien – Necropsy (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 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.

Exigences

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

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

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

Informations spécifiques au rôle

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

Pourquoi Charles River ?

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

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

À propos de Safety Assessment

Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

À propos de Charles River

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Description du poste

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Chef d’équipe, exploitation

Informations sur le poste

Date : Jun 21, 2026
Location : La Salle, QC, CA, H8N 1X1
Identifiant de la demande : 290544
Nom/numéro du magasin : QC-Carrefour Angrignon (1514)
Adresse : 7077 Newman Blvd, La Salle, QC H8N 1X1, Canada (CA)
Type demploi : Full Time
Type de poste : Regular
Statut du poste vacant : ce poste correspond à un poste vacant existant

Description du poste

En tant que chef déquipe, exploitation, vous devrez gérer tous les aspects de lexploitation dun magasin Sephora précis. Cela comprend la gestion de tous les membres de léquipe exploitation. De plus, vous soutiendrez régulièrement la dotation de léquipe exploitation, léquipe chargée des stocks pendant la nuit, léquipe de direction de lexploitation et lexécution générale des activités de Sephora.

• Assurer lexcellence opérationnelle. Diriger les activités dexploitation du magasin. Voir à la bonne exécution de lensemble des processus visant lexploitation du magasin, conformément aux normes de lentreprise
• Gérer les stocks. Gérer les stocks du magasin. Cela comprend lexpédition, la réception, le retour de la marchandise, le dénombrement périodique et la vérification de la conformité de tous les processus avec les directives de lentreprise et dans les délais impartis
• Marchandisage visuel. Gérer les concepts de marchandisage et les éléments visuels sur scène pour quils soient conformes aux normes de lentreprise. Gérer toutes les équipes de nettoyage internes ou tierces et veiller à ce quelles respectent les normes convenues en leur donnant de la rétroaction, de lencadrement et en transmettant les problèmes à une instance supérieure, au besoin
• Gestion de lapprovisionnement. Gérer le processus nécessaire au maintien du budget et de la quantité de fournitures, de démonstrateurs et déchantillons appropriés pour le magasin
• Évaluer le rendement et le perfectionnement. Participer à la gestion de toutes les situations exigeant une gestion du rendement au sein de léquipe exploitation. Veiller à ce que les membres de léquipe reçoivent en temps opportun de la rétroaction à des fins damélioration et assurer un suivi, le cas échéant
• Être passionné par les clients. Agir régulièrement à titre de responsable en service dans le magasin. Collaborer dans la mesure du possible avec les conseillers beauté et les clients dans laire de vente

Qualifications et expérience

• Vous possédez 1-3 ans dexpérience dans un rôle similaire dans un magasin ayant un volume de vente équivalent ou de lexpérience interne équivalente
• Vous avez une capacité éprouvée à influencer vos pairs et à donner de la rétraction
• Vous avez dexcellentes aptitudes en exploitation de magasin
• Vous avez fait preuve dune gestion efficace du temps et de compétences en résolution de problèmes

Récompenses significatives

La rémunération varie entre 21.10 $ CA et 26.40/hr $ CA. De plus, vous bénéficierez de primes de rendement, d'un programme d'avantages sociaux concurrentiel et d'initiatives de formation et de perfectionnement solides visant à promouvoir le soutien et la reconnaissance des employés. La rémunération finale offerte dépendra de divers critères, y compris, mais sans s'y limiter, les qualifications et l'expérience réelles de la personne, ainsi que tout autre critère opérationnel légitime et non discriminatoire pertinent au poste ou à l'emplacement.

Sephora Canada s'engage à fournir des accommodements raisonnables aux candidat(e)s handicapé(e)s ou souffrant d'autres problèmes médicaux.

Dans le cadre de notre engagement en faveur de la transparence et de l'efficacité, nous tenons à vous informer que nous utilisons des technologies d'intelligence artificielle (IA) dans notre processus de recrutement pour faciliter la présélection et l'évaluation initiales des candidatures.

Job Segment: Equipment Operator, Manufacturing, Operations

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 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 spécifiques au poste

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

Pourquoi Charles River ?

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

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.

A 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.

A propos de Charles River

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Charles River

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Description du poste

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

In this role, primary responsibilities include:

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

Qualifications minimales

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 poste

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

Pourquoi Charles River ?

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

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

À propos de Safety Assessment

Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

À propos de Charles River

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Ce que nous offrons

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Description du poste

Qui nous sommes

BM Digital est une société de croissance technologique, alimentée par Meteoric AI, notre plateforme exclusive d’intelligence pour influenceurs et médias payants - et nous opérons à une échelle que la plupart des entreprises de croissance n’atteignent jamais.

Nous gérons 80 000+ partenariats avec des créateurs chaque mois, supervisons 500 M$+ de dépenses médiatiques annuelles sur Meta et TikTok, et travaillons exclusivement avec des marques de consommation à forte croissance.

Si vous avez fait passer des comptes Meta de 20k $ par jour à 300k+/jour, et que vous savez exactement pourquoi cela a fonctionné et comment le reproduire - nous voulons avoir de vos nouvelles.

Le rôle

Nous recherchons un Head of Growth qui a été profondément impliqué dans le quotidien du scaling agressif des médias payants et qui sait ce qu’il faut réellement pour pousser efficacement les dépenses Meta à grande échelle.

Vous comprenez comment l’algorithme de Meta réagit à la vitesse de création, à l’architecture de contrôle des coûts, à la structure d’audience, et à l’augmentation du budget - et vous pouvez traduire cette compréhension en une croissance durable et cumulative sur un portefeuille de clients DTC.

Vous serez responsable de la stratégie de croissance sur l’ensemble d’un portefeuille, dirigerez une équipe d’analystes en médias payants et de stratèges créatifs, et serez la voix senior lors des échanges avec les clients quand il faut quelqu’un capable d’observer un compte et de voir non seulement ce qui se passe, mais aussi ce qui doit se passer ensuite pour débloquer le prochain niveau d’échelle.

Ce que vous aurez en charge

Scaling Meta agressif et efficace - monter jusqu’à des six chiffres par jour lorsque l’économie unitaire le permet.

Vous connaissez la différence entre scaler parce que les données disent d’y aller et scaler parce qu’un client vous l’a demandé.

Vous ne confondez jamais les deux.

Stratégie de médias payants full-funnel sur Meta, Google et TikTok - avec une hiérarchie claire sur où pousser et où protéger la marge.

Vous pouvez diagnostiquer les problèmes de performance au niveau de la création, de l’audience, de l’offre, de la landing page, ou du checkout - et vous savez lequel corriger en premier.

Leadership de la stratégie créative aux côtés de notre équipe créative.

Vous comprenez qu’à grande échelle, la création est le levier principal, et vous avez un point de vue solide sur ce qui fait qu’un concept gagne avant même que les données ne reviennent.

Relations clients seniors sur un portefeuille de marques DTC à forte croissance.

Vous pouvez accompagner un fondateur sceptique à travers une stratégie de reset, défendre une décision de scaling avec des données, et gérer la tension entre l’efficacité à court terme et la croissance à long terme - sans perdre la confiance du client.

Développement de l’équipe - transformer les juniors analystes et stratèges en des opérateurs solides et indépendants.

Exigences

Preuve concrète d’un parcours de scaling des comptes Meta au-delà de 100k$/jour.

Vous pouvez expliquer précisément comment vous l’avez fait, ce qui s’est cassé, et comment vous l’avez corrigé.

• 6–10 ans en publicité digitale payante, avec une part significative de gestion de gros budgets Meta pour des marques e-commerce DTC.

Compréhension approfondie de la structure de l’algorithme de Meta - fatigue créative, interactions de contrôle des coûts, saturation de l’audience, dynamiques de CPM, et architecture des campagnes qui donne à l’algorithme ce dont il a besoin pour dépenser efficacement à grande échelle.

Rigueur analytique sans être paralysé par les données.

Vous prenez des décisions, vous avancez vite, et vous assumez la responsabilité des résultats.

Communicateur clair et direct - avec les clients, la direction et votre équipe, surtout lorsque la nouvelle n’est pas celle qu’ils veulent entendre.

Ce que nous offrons

Compensation & Localisation 150 000 – 300 000 USD de rémunération annuelle totale, incluant le salaire de base, la prime de performance et des actions Tout à distance - nous avons construit l’infrastructure pour des équipes distribuées hautes performances et nous faisons confiance à nos collaborateurs pour faire leur meilleur travail depuis l’endroit où ils travaillent le mieux Powered by JazzHR

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

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

Exigences liées au poste

• 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.

Charles River : amélioration de la qualité de vie

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.

Résumé 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 poste

• 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.

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 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.

Responsabilités principales

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 relatives au poste

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

Pourquoi Charles River ?

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

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

À propos de Safety Assessment

Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

À propos de Charles River

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

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.

Présentation de l’entreprise

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Description du poste

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

In this role, primary responsibilities include:

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

Exigences 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 rôle

Role Specific Information:

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Annual bonus based on performance;
• Schedule: Monday to Friday 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.

Ce que nous offrons

Why Charles River ?

• We offer competitive benefits and advantages from day one to support your well-being;
• Paid development training;
• Employee and family assistance program;
• Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
• Access to a doctor and various health professionals (telemedicine);
• 3 weeks’ Vacation & 10 Personal day policy;
• Many social activities!

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

À propos 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

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 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.

Exigences minimales

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

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

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

Informations spécifiques au rôle

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

Pourquoi Charles River ?

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

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

À propos de Safety Assessment

Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

À propos de Charles River

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Ce que nous offrons

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Présentation de l’entreprise

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.

Exigences

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.

Aperçu du poste

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.

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);
• 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.

Technician – Necropsy (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 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.

Exigences 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.

Why Charles River ?

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

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

About Safety Assessment

Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

About Charles River

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.