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CM
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Actalent

Mechanical Test Engineer

Vancouver, BC, Canada

$48 to $57 CAD / hour · Contract

Apply About employer

Applications open in a new tab.

Job details

Pay: $48 to $57 CAD / hour
Job type: Contract
Apply by: Nov 9, 2026
Experience: 8+ years of test/design/systems engineering experience in a product development environment, particularly within medical device R&D.
Posting language: English · French
Posted: Oct 10, 2026

Original job description

English section of this bilingual listing.

Job Description

The Mechanical Test Engineer is responsible for supporting new product development programs by delivering product design verification. This role requires close interaction with cross-functional teams including design, manufacturing, quality, regulatory, and program management.

Responsibilities

Manage and complete design verification activities for multiple new product development programs.
Develop a project plan for design verification based on program scope, including deliverables, timelines, and resource needs.
Identify, ideate, and oversee the development of novel engineering test methods and fixtures.
Oversee the development of verification plans, protocols, and reports.
Peer-review and provide feedback on team deliverables for technical soundness and audit-readiness.
Oversee technical and schedule communication with internal and external partners to efficiently manage and mitigate risks.
Collaborate with test engineers, design engineers, and cross-functional teams to analyze product test failures and recommend solutions.
Provide critical updates to management.
Develop and maintain subject matter expertise in applicable technical standards for medical device development.
Identify and implement improvements to the verification test system through standardization, tools, and automation.
Ensure deliverables comply with applicable regulatory standards.
Follow quality management system and documentation practices.
Ensure completion of tasks within the project schedule with high attention to detail.

Essential Skills

Bachelors degree in engineering (mechanical, mechatronics, or similar); Advanced degree preferred.
P.Eng from the EGBC preferred; ability and willingness to obtain a P.Eng license required.
8+ years of test/design/systems engineering experience in a product development environment, particularly within medical device R&D.
Strong analytical foundation using engineering principles for problem-solving during new product development.
Hands-on experience developing and qualifying engineering test methods and tools.
Hands-on experience with developing electromechanical systems and root cause analysis.
Experience managing and delivering design verification in a highly regulated industry.
Experience using project planning tools and concepts.
Experience using statistical techniques, preferably using Minitab.
Proficient in writing concisely and accurately with meticulous attention to detail and clarity.
Strong verbal and written communication skills suitable for a cross-functional environment.
Ability to work within tight deadlines with transparent communication.
Familiarity with CAD tools and microcontrollers (e.g., Arduino); hands-on experience preferred.
Familiarity with medical device applicable technical and regulatory standards; hands-on experience preferred.

Additional Skills & Qualifications

Experience with requirements management and issue tracking tools preferred.
For applicants without an Engineer in Training or a Professional Engineer license, an alternative title will be used until a license is obtained.
Support for job-related professional growth and development, including reimbursements for expenses incurred in joining the EGBC.

Job Type & Location

This is a Contract position based out of Vancouver, BC.

Pay And Benefits

The pay range for this position is $48.08 - $57.69/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.

Workplace Type

This is a fully onsite position in Vancouver,BC.

À propos d'Actalent

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

Manage and complete design verification activities for multiple new product development programs.
Develop a project plan for design verification based on program scope, including deliverables, timelines, and resource needs.
Identify, ideate, and oversee the development of novel engineering test methods and fixtures.
Oversee the development of verification plans, protocols, and reports.
Peer-review and provide feedback on team deliverables for technical soundness and audit-readiness.
Oversee technical and schedule communication with internal and external partners to efficiently manage and mitigate risks.
Collaborate with test engineers, design engineers, and cross-functional teams to analyze product test failures and recommend solutions.
Provide critical updates to management.
Develop and maintain subject matter expertise in applicable technical standards for medical device development.
Identify and implement improvements to the verification test system through standardization, tools, and automation.
Ensure deliverables comply with applicable regulatory standards.
Follow quality management system and documentation practices.
Ensure completion of tasks within the project schedule with high attention to detail.

Essential Skills

Bachelors degree in engineering (mechanical, mechatronics, or similar); Advanced degree preferred.
P.Eng from the EGBC preferred; ability and willingness to obtain a P.Eng license required.
8+ years of test/design/systems engineering experience in a product development environment, particularly within medical device R&D.
Strong analytical foundation using engineering principles for problem-solving during new product development.
Hands-on experience developing and qualifying engineering test methods and tools.
Hands-on experience with developing electromechanical systems and root cause analysis.
Experience managing and delivering design verification in a highly regulated industry.
Experience using project planning tools and concepts.
Experience using statistical techniques, preferably using Minitab.
Proficient in writing concisely and accurately with meticulous attention to detail and clarity.
Strong verbal and written communication skills suitable for a cross-functional environment.
Ability to work within tight deadlines with transparent communication.
Familiarity with CAD tools and microcontrollers (e.g., Arduino); hands-on experience preferred.
Familiarity with medical device applicable technical and regulatory standards; hands-on experience preferred.

Additional Skills & Qualifications

Experience with requirements management and issue tracking tools preferred.
For applicants without an Engineer in Training or a Professional Engineer license, an alternative title will be used until a license is obtained.
Support for job-related professional growth and development, including reimbursements for expenses incurred in joining the EGBC.

Work Environment

The work environment involves collaboration with cross-functional teams using advanced engineering tools and technologies. The position requires adherence to high standards of regulatory compliance and quality management systems. The role is dynamic, involving interactions with internal and external partners to manage projects efficiently.

Job Type & Location

This is a Contract position based out of Vancouver, BC.

Pay And Benefits

The pay range for this position is $48.08 - $57.69/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.

Workplace Type

This is a fully onsite position in Vancouver,BC.

À propos d'Actalent

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.

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.

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

Manage design verification for multiple medical device development programs, including project plans, test methods, fixtures, protocols, reports, and schedule and risk communications. Analyze test failures with cross-functional teams, provide technical reviews and management updates, and improve verification systems while ensuring regulatory and quality compliance.

Requirements

A bachelor's degree in mechanical, mechatronics, or similar engineering is required, with an advanced degree preferred; an EGBC Professional Engineer license is preferred, and willingness to obtain one is required. Candidates need 8+ years of product development engineering experience, preferably in medical device R&D, along with hands-on test method development, design verification, electromechanical systems, root cause analysis, and strong communication and analytical skills.

Skills

Design Verification
Test Method Development
Test Fixture Development
Project Planning
Root Cause Analysis
Electromechanical Systems
Statistical Analysis
Minitab
Regulatory Compliance
Medical Device Standards
Requirements Management
Issue Tracking
CAD
Microcontrollers
Cross-Functional Communication
Quality Management Systems

Benefits

Professional Growth And Development Support
Reimbursement For EGBC Membership Expenses

Visa sponsorship

Not detected in the job text

Keywords

Design Verification
Medical Device Development
Product Development
Test Engineering
Test Methods
Test Fixtures
Verification Plans
Test Protocols
Verification Reports
Project Planning
Risk Management
Root Cause Analysis
Electromechanical Systems
Statistical Techniques
Minitab
CAD
Arduino
Microcontrollers
Requirements Management
Issue Tracking
Regulatory Standards
Quality Management Systems
EGBC
Professional Engineer License
Design Engineering
Manufacturing
Quality Assurance
Cross-Functional Teams

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