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Added 21 mins ago
Maintenance Technician Associate
Opta Group
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SUSTAINABILITY: We engineer solutions with efficiency, responsibility, and sustainability as our foundation, optimizing performance today, while strengthening the resilience of tomorrow's…
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Added 51 mins ago
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Site Operations Manager
AML Oceanographic Ltd.
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- $100,000 to $125,000 CAD / year
- Full-time
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Spécialiste Qualité Fournisseurs
Actalent
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- $40 to $55 CAD / hour
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Mechanical Engineer
Actalent
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- $45 to $75 CAD / hour
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We are seeking a Mechanical Engineer or experienced Mechanical Designer to support a time-sensitive reverse engineering project. You measure a machine, recreate it as a precise 3D CAD model…
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Spécialiste Qualité Fournisseurs
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Ingénieur En Qualité/Software Quality Engineer
Actalent
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- $39 to $57 CAD / hour
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The Software Quality Engineer will join the Software Quality department supporting engine programs. This group is responsible for reviewing software delivered by internal software teams and…
Added 51 mins ago
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Manufacturing Engineer
Actalent
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- $45 to $55 CAD / hour
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The Manufacturing Engineer plays a key role in improving dimensional quality for body and general assembly parts and subassemblies in both launch and steady-state production. This role…
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The Process Engineer - SMT Support is responsible for developing, optimizing, and sustaining surface mount technology (SMT) manufacturing processes used in the production of broadcast and…
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Electronics Engineer
Actalent
Calgary, AB
- $52 to $60 CAD / hour
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…individual's contributions are recognized. As an Electronics Engineer, you will have the opportunity to make a significant impact in education, business, and beyond by developing products…
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Actalent

Test Engineer

Quebec, QC, Canada

$40 to $58 CAD / hour · Contract

Apply About employer

Applications open in a new tab.

Job details

Pay: $40 to $58 CAD / hour
Job type: Contract
Apply by: Nov 29, 2026
Posting language: English · French
Posted: Oct 30, 2026

Original job description

English section of this bilingual listing.

Job Title: Validation & Verification (V&V) Engineer Job Description

The V&V Engineer is responsible for planning, executing, documenting, and reporting verification and validation activities for medical devices and associated software systems. You will work closely with R&D, Quality Assurance, Regulatory Affairs, Manufacturing Engineering, and Product Management teams to ensure products meet design requirements, regulatory standards, and customer expectations.

Responsibilities

Develop and maintain Verification & Validation plans, protocols, test methods, and reports.
Execute design verification testing to confirm compliance with product requirements.
Support design validation activities to ensure devices satisfy intended use and user needs.
Conduct integration, system, performance, reliability, environmental, and usability testing.
Analyze test results and document findings in accordance with quality system procedures.
Review product requirements and design inputs for testability.
Create and maintain traceability matrices between requirements, risks, and verification activities.
Ensure complete verification coverage across all product requirements.
Participate in risk assessments and FMEA activities.
Verify effectiveness of risk control measures.
Support regulatory submissions through preparation of verification and validation documentation.
Support product risk management activities in accordance with ISO & FDA regulations.

Essential Skills

7 years of testing experience with test cases, test protocols, test plan, test scenarios, functional testing.
3 years of lab test setup experience.
3 years of safety-critical documentation.
Experience in software testing, validation, MATLAB.

Additional Skills and Qualifications

Medical experience.
Proficiency in Python.
Optic knowledge.
French language proficiency required.

Job Type & Location

This is a Contract position based out of Quebec, QC.

Pay And Benefits

The pay range for this position is $40.00 - $58.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Job Type & Location

This is a Contract position based out of Quebec, QC.

Workplace Type

This is a hybrid position in Quebec,QC.

À propos dActalent

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Read the full bilingual original

Titre du poste: Ingénieur Validation et Vérification (V&V) Description du poste

L'ingénieur V&V est responsable de la planification, de l'exécution, de la documentation et du reporting des activités de vérification et de validation pour les dispositifs médicaux et les systèmes logiciels associés. Vous travaillerez en étroite collaboration avec les équipes de R&D, Assurance Qualité, Affaires Réglementaires, Ingénierie de Fabrication et Gestion de Produits pour garantir que les produits répondent aux exigences de conception, normes réglementaires et attentes des clients.

Responsabilités

Développer et maintenir des plans, protocoles, méthodes de test et rapports de Vérification & Validation.
Exécuter des tests de vérification de conception pour confirmer la conformité aux exigences du produit.
Soutenir les activités de validation de la conception pour garantir que les dispositifs répondent à l'utilisation prévue et aux besoins des utilisateurs.
Conduire des tests d'intégration, de système, de performance, de fiabilité, environnementaux et de convivialité.
Analyser les résultats des tests et documenter les conclusions conformément aux procédures du système de qualité.
Revoir les exigences du produit et les entrées de conception pour leur testabilité.
Créer et maintenir des matrices de traçabilité entre les exigences, les risques et les activités de vérification.
Assurer une couverture complète de la vérification sur toutes les exigences du produit.
Participer aux évaluations des risques et aux activités FMEA.
Vérifier l'efficacité des mesures de contrôle des risques.
Soutenir les soumissions réglementaires par la préparation de la documentation de vérification et de validation.
Soutenir les activités de gestion des risques produits conformément aux réglementations ISO & FDA.

Compétences Essentielles

7 ans d'expérience en test avec des cas de test, protocoles de test, plans de test, scénarios de test, tests fonctionnels.
3 ans d'expérience en configuration de tests en laboratoire.
3 ans de documentation critique pour la sécurité.
Expérience en ingénierie logicielle, validation, MATLAB.

Compétences Supplémentaires & qualifications

Expérience médicale.
Compétences en Python.
Connaissances en optique.
Maîtrise du français obligatoire.

Environnement De Travail

Le bureau est situé à Québec, avec une présence requise de 3 jours sur site pour les jours de test. Vous travaillerez sur des dispositifs médicaux cardiovasculaires innovants utilisés mondialement pour améliorer les résultats des patients.

Type de poste & Emplacement

Ce poste Contract est basé à Quebec, QC.

Taux de rémunération & Avantages

La fourchette salariale associée à ce poste est de $40.00 - $58.00/hr.

La rémunération individuelle offerte pour ce poste, à lintérieur de cette fourchette, dépendra de nombreux facteurs, notamment les qualifications, les compétences, lexpérience pertinente, la connaissance du poste, la localisation géographique, léquité interne ainsi que dautres facteurs pertinents liés au poste.

Type de poste & Emplacement

Ce poste Contrat (temporaire) est basé à Quebec, QC.

Type de milieu de travail

Il s'agit d'un poste hybrid, situé à Quebec,QC.

Job Title: Validation & Verification (V&V) Engineer Job Description

The V&V Engineer is responsible for planning, executing, documenting, and reporting verification and validation activities for medical devices and associated software systems. You will work closely with R&D, Quality Assurance, Regulatory Affairs, Manufacturing Engineering, and Product Management teams to ensure products meet design requirements, regulatory standards, and customer expectations.

Responsibilities

Develop and maintain Verification & Validation plans, protocols, test methods, and reports.
Execute design verification testing to confirm compliance with product requirements.
Support design validation activities to ensure devices satisfy intended use and user needs.
Conduct integration, system, performance, reliability, environmental, and usability testing.
Analyze test results and document findings in accordance with quality system procedures.
Review product requirements and design inputs for testability.
Create and maintain traceability matrices between requirements, risks, and verification activities.
Ensure complete verification coverage across all product requirements.
Participate in risk assessments and FMEA activities.
Verify effectiveness of risk control measures.
Support regulatory submissions through preparation of verification and validation documentation.
Support product risk management activities in accordance with ISO & FDA regulations.

Essential Skills

7 years of testing experience with test cases, test protocols, test plan, test scenarios, functional testing.
3 years of lab test setup experience.
3 years of safety-critical documentation.
Experience in software testing, validation, MATLAB.

Additional Skills and Qualifications

Medical experience.
Proficiency in Python.
Optic knowledge.
French language proficiency required.

Work Environment

The office is located in Quebec City with a requirement to be on-site for 3 days during testing days. You will be working on innovative cardiovascular medical devices that are used globally to improve patient outcomes.

Job Type & Location

This is a Contract position based out of Quebec, QC.

Pay And Benefits

The pay range for this position is $40.00 - $58.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Job Type & Location

This is a Contract position based out of Quebec, QC.

Workplace Type

This is a hybrid position in Quebec,QC.

À propos dActalent

Actalent est un leader mondial dans les services dingénierie et de sciences ainsi que dans les solutions de talents. Nous aidons des entreprises visionnaires à faire progresser leurs initiatives dingénierie et de science grâce à laccès à des experts spécialisés qui favorisent léchelle, linnovation et la rapidité de mise sur le marché. Avec un réseau de près de 20 000 consultants et 5 000 clients à travers les États-Unis, le Canada, lAsie et lEurope, Actalent dessert de nombreuses entreprises du Fortune 500. Nous sommes fiers dêtre lune des 500 meilleures firmes de conception de lEngineering News-Record (ENR) pour nos services de conception en ingénierie et un lauréat du prix ClearlyRated Best of Staffing® tant pour le service client que pour les talents.

Actalent est un employeur souscrivant au principe de légalité des chances et accepte toutes les candidatures sans tenir compte de la race, du sexe, de lâge, de la couleur, de la religion, des origines nationales, du statut dancien combattant, dun handicap, de lorientation sexuelle, de lidentité sexuelle, des renseignements génétiques ou de toute autre caractéristique protégée par la loi.

Si vous souhaitez faire une demande daccommodement raisonnable, tel que la modification ou lajustement du processus de demande demploi ou dentrevue à cause dun handicap, veuillez envoyer un courriel à actalentaccommodation@actalentservices.com pour connaître dautres options daccommodement.

Numéro du permis d'agence de placement de personnel : AP-2000486 (Canada Québec)

Numéro du permis d'agence de recrutement de travailleurs étrangers temporaires : AR-2000485 (Canada Québec)

Ordonnance sur légalité des chances de San Francisco: Conformément à lOrdonnance sur légalité des chances de San Francisco, pour tous les postes situés dans la ville et le comté de San Francisco, nous examinerons les candidatures des personnes qualifiées ayant un casier judiciaire ou des antécédents criminels.

Utilisation de lintelligence artificielle (IA): Nous pouvons utiliser lintelligence artificielle (IA) pour soutenir certaines étapes de notre processus dembauche, notamment la recherche, la présélection et lévaluation des candidatures. LIA aide à analyser les candidatures et les qualifications, mais les décisions finales sont prises par notre équipe de recrutement. En soumettant votre candidature, vous reconnaissez et acceptez que celle-ci puisse être examinée à laide doutils dIA.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Personnel Placement Agency Permit Number: AP-2000486 (Canada Quebec)

Temporary Foreign Worker Recruitment Agency Permit Number: AR-2000485 (Canada Quebec)

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Apply About employer

More about this job

Responsibilities

Plan, execute, document, and report verification and validation activities for cardiovascular medical devices and associated software, including integration, system, performance, reliability, environmental, and usability testing. Maintain requirements and risk traceability, assess test results and risk controls, and prepare documentation supporting regulatory submissions.

Requirements

Requires seven years of testing experience, including test cases, protocols, plans, scenarios, and functional testing, plus three years of laboratory test setup and safety-critical documentation experience. Experience in software testing, validation, and MATLAB is required; medical experience, Python, optics knowledge, and French proficiency are also listed, with French proficiency stated as mandatory.

Skills

Verification And Validation
Test Planning
Test Protocols
Test Cases
Functional Testing
Laboratory Test Setup
Software Testing
MATLAB
Python
Medical Device Testing
Design Verification
Design Validation
Risk Management
FMEA
Requirements Traceability
French Proficiency

Visa sponsorship

Not detected in the job text

Keywords

Verification And Validation
Medical Devices
Cardiovascular Devices
Software Systems
Test Plans
Test Protocols
Test Methods
Test Cases
Test Scenarios
Functional Testing
Laboratory Test Setup
Design Verification
Design Validation
Integration Testing
System Testing
Performance Testing
Reliability Testing
Environmental Testing
Usability Testing
Requirements Traceability
Risk Management
FMEA
Quality System Procedures
Regulatory Submissions
ISO Regulations
FDA Regulations
MATLAB
Python
Optics
French

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