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Added 13 mins ago
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Project Engineer/Analyst
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- Full-time
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- $150,000 to $185,000 CAD / year
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Technology Lead - GenAI Lead
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Actalent

Systems Test Engineer

Montreal, QC, Canada

$40 to $50 CAD / hour · Contract

Apply About employer

Applications open in a new tab.

Job details

Pay: $40 to $50 CAD / hour
Job type: Contract
Apply by: Dec 2, 2026
Posting language: English · French
Posted: Nov 2, 2026

Original job description

English section of this bilingual listing.

Job Title: Test Engineer

Job Description

Join a leading biomedical engineering firm specializing in medical devices used in interventional medical specialties. This role involves working on the Guardian project, a remediation initiative to ensure compliance with FDA standards, focusing on catheter medical devices.

Responsibilities

Review and remediate extensive volumes of system and software test requirements.
Evaluate test requirements line-by-line to identify gaps, ambiguities, and inconsistencies.
Rewrite test requirements to ensure clarity, testability, traceability, and compliance.
Maintain and improve test documentation traceability and align with Design History File (DHF).
Collaborate with the Quality team to identify documentation deficiencies and define remediation scope.
Execute corrective actions independently and support audit/readiness activities as needed.
Analyze historical product changes and documentation to ensure updated documentation reflects current systems.
Contribute to product/system-level risk analysis and support updates to Risk files.
Identify systemic issues in documentation practices and propose improved engineering processes.
Standardize writing practices and documentation workflows to align with test strategies and verification activities.

Essential Skills

Proficiency in requirement writing and specification documents.
Experience in systems design and engineering.
Knowledge of documentation review and test requirement design.
Understanding of regulated documentation, preferably in the medical field.
Troubleshooting skills and experience in Test Method Validation.
Familiarity with functional test, electrical electronic systems, and medical equipment.
Experience in biomedical engineering and quality assurance.
Familiarity with IEC, ISO, and ISO/IEEE standards.
1 year of experience in regulated documentation, preferably medical.
1 year of experience in troubleshooting.
1 year of experience working with electrical electronic systems.
Understanding of stages in Test Method Validation.
Experience in biomedical engineering is an asset.
Experience with user manuals and test requirements is an asset.

Work Environment

Hybrid work environment with 4 to 5 days in the office, primarily on Tuesday, Wednesday, and Thursday. Additional office days may be required depending on project needs.

Job Type & Location

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

Pay And Benefits

The pay range for this position is $40.00 - $50.00/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 Montreal, QC.

Workplace Type

This is a hybrid position in Montreal,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 de Test

Description Du Poste

Rejoignez une entreprise de génie biomédical de premier plan spécialisée dans les dispositifs médicaux utilisés dans les spécialités médicales interventionnelles. Ce rôle implique de travailler sur le projet Guardian, une initiative de remédiation pour garantir la conformité aux normes de la FDA, en se concentrant sur les dispositifs médicaux de type cathéter.

Responsabilités

Examiner et remédier à de grands volumes de exigences de test système et logiciel.
Évaluer les exigences de test ligne par ligne pour identifier les lacunes, ambiguïtés et incohérences.
Réécrire les exigences de test pour assurer la clarté, la testabilité, la traçabilité et la conformité.
Maintenir et améliorer la traçabilité de la documentation de test et s'aligner sur le dossier de l'historique de conception (DHF).
Collaborer avec l'équipe qualité pour identifier les déficiences de documentation et définir la portée de la remédiation.
Exécuter des actions correctives de manière indépendante et soutenir les activités d'audit/préparation si nécessaire.
Analyser les changements de produits historiques et la documentation pour garantir que la documentation mise à jour reflète les systèmes actuels.
Contribuer à l'analyse des risques au niveau du produit/système et soutenir les mises à jour des fichiers de risques.
Identifier les problèmes systémiques dans les pratiques de documentation et proposer des processus d'ingénierie améliorés.
Standardiser les pratiques d'écriture et les flux de travail de documentation pour s'aligner sur les stratégies de test et les activités de vérification.

Compétences Essentielles

Maîtrise de la rédaction des exigences et des documents de spécification.
Expérience dans la conception et l'ingénierie de systèmes.
Connaissance de la révision de documentation et de la conception des exigences de test.
Compréhension de la documentation réglementée, de préférence dans le domaine médical.
Compétences en dépannage et expérience dans la validation des méthodes de test.
Connaissance des tests fonctionnels, des systèmes électroniques électriques et des équipements médicaux.
Formation en ingénierie biomédicale et assurance qualité.
Familiarité avec les normes IEC, ISO et ISO/IEEE.

Compétences Supplémentaires & Qualifications

Au moins 1 an d'expérience dans la conception des exigences de test.
1 an d'expérience dans la conception de systèmes de test.
1 an d'expérience dans la documentation réglementée, de préférence médicale.
1 an d'expérience en dépannage.
1 an d'expérience de travail avec les systèmes électroniques électriques.
Compréhension des étapes de la validation des méthodes de test.
Expérience en ingénierie biomédicale est un atout.
Expérience avec les manuels d'utilisation et les exigences de test est un atout.

Environnement De Travail

Environnement de travail hybride avec 4 à 5 jours au bureau, principalement mardi, mercredi et jeudi. Des jours supplémentaires au bureau peuvent être nécessaires en fonction des besoins du projet.

Type de poste & Emplacement

Ce poste Contract est basé à Montreal, QC.

Taux de rémunération & Avantages

La fourchette salariale associée à ce poste est de $40.00 - $50.00/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 Montreal, QC.

Type de milieu de travail

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

Job Title: Test Engineer

Job Description

Join a leading biomedical engineering firm specializing in medical devices used in interventional medical specialties. This role involves working on the Guardian project, a remediation initiative to ensure compliance with FDA standards, focusing on catheter medical devices.

Responsibilities

Review and remediate extensive volumes of system and software test requirements.
Evaluate test requirements line-by-line to identify gaps, ambiguities, and inconsistencies.
Rewrite test requirements to ensure clarity, testability, traceability, and compliance.
Maintain and improve test documentation traceability and align with Design History File (DHF).
Collaborate with the Quality team to identify documentation deficiencies and define remediation scope.
Execute corrective actions independently and support audit/readiness activities as needed.
Analyze historical product changes and documentation to ensure updated documentation reflects current systems.
Contribute to product/system-level risk analysis and support updates to Risk files.
Identify systemic issues in documentation practices and propose improved engineering processes.
Standardize writing practices and documentation workflows to align with test strategies and verification activities.

Essential Skills

Proficiency in requirement writing and specification documents.
Experience in systems design and engineering.
Knowledge of documentation review and test requirement design.
Understanding of regulated documentation, preferably in the medical field.
Troubleshooting skills and experience in Test Method Validation.
Familiarity with functional test, electrical electronic systems, and medical equipment.
Experience in biomedical engineering and quality assurance.
Familiarity with IEC, ISO, and ISO/IEEE standards.

Additional Skills And Qualifications

At least 1 year of experience in test requirement design.
1 year of experience in test systems design.
1 year of experience in regulated documentation, preferably medical.
1 year of experience in troubleshooting.
1 year of experience working with electrical electronic systems.
Understanding of stages in Test Method Validation.
Experience in biomedical engineering is an asset.
Experience with user manuals and test requirements is an asset.

Work Environment

Hybrid work environment with 4 to 5 days in the office, primarily on Tuesday, Wednesday, and Thursday. Additional office days may be required depending on project needs.

Job Type & Location

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

Pay And Benefits

The pay range for this position is $40.00 - $50.00/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 Montreal, QC.

Workplace Type

This is a hybrid position in Montreal,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

Review and remediate system and software test requirements, improving their clarity, testability, traceability, and regulatory compliance. Maintain and align test documentation with the Design History File, support quality and audit activities, contribute to risk analysis, and improve documentation processes.

Requirements

Candidates should have at least one year of experience in test requirement design, test systems design, regulated documentation, troubleshooting, and electrical or electronic systems. The role also calls for knowledge of test method validation, functional testing, medical equipment, quality assurance, and relevant IEC, ISO, and ISO/IEEE standards; biomedical engineering experience is an asset.

Skills

Test Requirement Design
Requirements Writing
Systems Design
Systems Engineering
Documentation Review
Regulated Documentation
Test Method Validation
Troubleshooting
Functional Testing
Electrical and Electronic Systems
Medical Equipment
Biomedical Engineering
Quality Assurance
Risk Analysis
Traceability
IEC, ISO, and ISO/IEEE Standards

Visa sponsorship

Not detected in the job text

Keywords

Medical Devices
Catheter Devices
FDA Compliance
Guardian Project
System Testing
Software Testing
Test Requirements
Test Systems Design
Requirements Writing
Test Method Validation
Design History File
Regulated Documentation
Traceability
Corrective Actions
Audit Readiness
Risk Analysis
Risk Files
Functional Testing
Electrical and Electronic Systems
Medical Equipment
Biomedical Engineering
Quality Assurance
IEC Standards
ISO Standards
ISO/IEEE Standards
Verification
User Manuals

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