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Added 2 mins ago
CC
GRADE PERSON
Conwest Contracting
Vancouver, BC
- Full-time
Ability to identify any design conflicts that may arise and report to the site supervisor.
Added 2 mins ago
M
Senior Full Stack Java Engineer - Workforce Management (WFM)
Miratech
Canada
- Full-time
We are looking for a Senior Full Stack Engineer to join the Workforce Management product stream and build enterprise-scale solution supporting forecasting, capacity planning, scheduling,…
Added 2 mins ago
C
Geotechnical Engineer
CIMA+
Montreal, QC
- Full-time
…what’s expected of us to meet the challenges of tomorrow and engineer a better…
Added 2 mins ago
TS
Fire Protection Engineer - Electrical (P.Eng), Relocation Assistance Available
TalentSphere Staffing Solutions
Toronto, ON
- Full-time
This role is ideal for an engineer with a strong background in fire alarm system design, fire and life safety engineering, and building code compliance. You will work on a diverse portfolio…
Added 2 mins ago
TS
Fire Protection Engineer - Mechanical (P.Eng), Relocation Assistance Available
TalentSphere Staffing Solutions
Mississauga, ON
- Full-time
This role is ideal for a mechanical engineer with a strong background in fire protection system design, sprinkler and standpipe systems, fire suppression, and building code compliance. You…
Added 2 mins ago
EI
DEVOPS & CLOUD INFRASTRUCTURE LEAD
EMERES INC.
Montreal, QC
- Full-time
Design, build, and maintain CI/CD pipelines for all engineering teams
Added 2 mins ago
PG
Mechanical Engineer
PACO Group
Longueuil, QC
- Full-time
At Groupe Paco, mechanical engineering takes amazing forms. Our teams design lifting systems for entertainment stages (Gala Systèmes), movable floors for swimming pools (Akvo Spiralift),…
Added 2 mins ago
AC
Pharmaceutical Facility Project Manager/Engineer
ALTEN Canada
Mississauga, ON
- $90,000 to $95,000 CAD / year
- Full-time
We are seeking a detail-oriented and proactive Facilities Engineer/ Pharmaceutical Construction PM with strong project management experience in a GMP-regulated environment. In this role,…
Added 2 mins ago
RI
Data Engineer
Rivago Infotech Inc
Toronto, ON
- Contract
We are seeking highly skilled Azure Data Engineer with strong expertise in SQL, Python, Datawarehouse, Cloud ETL tools to join our data team. The ideal candidate will design, implement and…
Added 2 mins ago
MV
Engineer-In-Training (Multiple Positions)
Metro Vancouver
Burnaby, BC
- $77,171.26 to $90,808.63 CAD / year
- Full-time
From the moment you join Metro Vancouver as an Engineer-in-Training, you’ll be contributing meaningful work on diverse, innovative and challenging projects, while sharing our vision for…
Added 2 mins ago
IG
Transmission line Engineer
Insight Global
Calgary, AB · Greater Calgary Metropolitan Area
- $75 to $80 CAD / hour
- Contract
We are seeking a Transmission Line Engineer to support the planning, design, analysis, and execution of high-voltage transmission line projects. The successful candidate will be responsible…
Added 14 mins ago
Project Engineer, Facilities MOP (Contract)
Trans Mountain
Calgary, AB
Trans Mountain is seeking a collaborative, motivated, and values driven individual to join our dynamic team as Project Engineer, Facilities MOP (Contract). In this position, you will play a…
Added 14 mins ago
Project Engineer, Pipeline MOP (Contract)
Trans Mountain
Calgary, AB
Trans Mountain is seeking a collaborative, motivated, and values driven individual to join our dynamic team as Project Engineer, Pipeline MOP (Contract). In this position, you will play a…
Added 14 mins ago
Senior Product Solutions Analyst
Scotiabank
Toronto, ON
…generative AI applications, including prompt engineering and design tailored for SGAM teams. The analyst will also collaborate with a range of third-party vendors to assess, integrate, and…
Added 14 mins ago
Engineer - Methods
Mitsubishi Heavy Industries, Ltd.
Mississauga, ON
Reporting to the Manager – Product Definition, the Engineer - Methods develops manufacturing integration concepts, determines assembly process/sequence, manufacturing bill of materials, and…
Added 14 mins ago
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Principal Firmware Engineer
Nokia
Ottawa, ON
- Full-time
In this role as a Principal Firmware Engineer, you will work within a dynamic Agile scrum team dedicated to innovation in optical systems. Collaborate closely with cross-functional teams,…
Added 26 mins ago
Backend Engineer, Payments & Risk
Stripe
Toronto, ON
Scope, design, build, and maintain APIs, services, and large-scale systems that reliably and efficiently handle billions of money movement requests
Added 26 mins ago
BB
Director of Engineering & Technical
Britespan Building Systems Inc
Kitchener, ON
- $140,000 to $160,000 CAD / year
- Full-time
Engineering quality, compliance and design standards
Added 26 mins ago
BB
Professional Engineer
Britespan Building Systems Inc
Kitchener, ON
- $115,000 to $130,000 CAD / year
- Full-time
We are looking for an experienced Professional Engineer to join our Engineering team and play a key role in the design, analysis, approval and continuous improvement of our innovative…
Added 26 mins ago
IO
Senior Engineer, Project Development
Irving Oil
Saint John, NB
- Full-time
As a Senior Engineer, you will support the development of capital projects by leading the front-end development stages (FEL 1 and 2) and supporting FEED / detailed engineering/execution…
Added 28 mins ago
Engineer 1-3 (Municipal Engineer)
The Government of Nova Scotia
Halifax, NS
As a Municipal Engineer, you will work closely with the Senior Engineer and report to the Manager of Municipal Infrastructure. You will provide technical engineering expertise in support of…
Added 28 mins ago
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Senior Azure Cloud Platform Engineer (Azure, Terraform, Power BI)
Recrute Action
Toronto, ON
- Contract
Senior Azure Cloud Platform Engineer (Azure, Terraform, Power BI)
Added 32 mins ago
IH
Platform Database RUN Engineer
InVita Healthcare Technologies
ON · Ontario, Canada
- $67,000 to $100,000 CAD / year
- Full-time
Added 32 mins ago
BS
Technical Lead
Brainhunter Systems Ltd
Toronto, ON
- Contract
8+ years building and operating complex enterprise digital products, including experience as a Technical Lead, Staff Engineer or senior full-stack developer.
Added 32 mins ago
GT
Data Analyst - ADF + Databricks
Global Technical Talent, an Inc. 5000 Company
Toronto, ON
- $90 to $95 CAD / hour
- Contract
…successful candidate will work on a daily basis with the Data Engineer Lead and client…

Zimmer Biomet

Quality Engineer I

Montreal, QC, Canada

Full-time

Apply About employer

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Job details

Job type: Full-time
Apply by: Nov 4, 2026
Posting language: English · French
Posted: Oct 5, 2026

Original job description

English section of this bilingual listing.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

What You Can Expect

Ensures Zimmer Biomet and compatible products meet regulatory, quality, and customer requirements throughout the design and development process, and product lifecycle. Collaborates cross-functionally and with external partners to achieve Zimmer Biomet’s quality and business objectives.

This position is on-site three days a week; however, increased on-site presence may be required during audit periods.

How You'll Create Impact

Works as part of a team, completing Quality tasks in the design and development, and change control processes.
Ensure compliance with global regulations and recognized standards (e.g., FDA 21 CFR Part 820, ISO 13485, ISO 14971, EU MDR).
Review, maintain and approve Design History Files (DHF) and Risk Management Files (RMF).
Identify and mitigate design risks using FMEA and other tools.
Support design verification and validation activities.
Supports design and change control processes.
Collaborate with design teams to embed quality standards.
Author, review and approve documentation in Quality capacity.
Define and control Critical to Quality (CTQ) characteristics.
Assist with regulatory submissions and audits.
Analyze quality data to identify trends and improvement areas.
Support quality improvement initiatives.
Support root cause investigations and CAPA activities.
Supports design transfer and sourcing transfers with Supplier Quality counterparts.
Supports customer complaints investigations.

What Makes You Stand Out

Experience in design controls, verification, validation (design, process and software).
Working knowledge of FDA 21 CFR 820.30, ISO 13485, and EU MDR.
Understanding of risk management (ISO 14971, FMEA, statistical tools).
Capable in V&V planning and execution including human factors usability studies.
Proficient in statistical data analysis.
Effective cross-functional communicator.
Excellent technical writing skills.
IT System Skills (Preferred Skills)

Your Background

Read the full bilingual original

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

What You Can Expect

Veille à ce que les produits de Zimmer Biomet et les produits compatibles respectent les exigences réglementaires, de qualité et des clients tout au long du processus de conception et de développement ainsi que du cycle de vie des produits. Collabore avec des équipes multidisciplinaires et des partenaires externes afin d’atteindre les objectifs de qualité et d’affaires de Zimmer Biomet.

Ce poste est basé sur site trois jours par semaine; toutefois, une présence accrue sur site peut être requise durant les périodes d’audit.

Ensures Zimmer Biomet and compatible products meet regulatory, quality, and customer requirements throughout the design and development process, and product lifecycle. Collaborates cross-functionally and with external partners to achieve Zimmer Biomet’s quality and business objectives.

This position is on-site three days a week; however, increased on-site presence may be required during audit periods.

How You'll Create Impact

Travaille au sein d’une équipe en réalisant des activités qualité dans le cadre des processus de conception, de développement et de contrôle des changements.
Assure la conformité aux réglementations mondiales et aux normes reconnues (p. ex., FDA 21 CFR Part 820, ISO 13485, ISO 14971, RDM de l’UE).
Révise, tient à jour et approuve les dossiers d’historique de conception (DHF) et les dossiers de gestion des risques (RMF).
Identifie et atténue les risques liés à la conception à l’aide de l’AMDEC (FMEA) et d’autres outils.
Soutient les activités de vérification et de validation de la conception.
Soutient les processus de conception et de contrôle des changements.
Collabore avec les équipes de conception afin d’intégrer les normes de qualité.
Rédige, révise et approuve la documentation dans le cadre de ses responsabilités en qualité.
Définit et contrôle les caractéristiques critiques pour la qualité (CTQ).
Participe aux soumissions réglementaires et aux audits.
Analyse les données qualité afin d’identifier les tendances et les occasions d’amélioration.
Soutient les initiatives d’amélioration de la qualité.
Soutient les enquêtes sur les causes fondamentales et les activités CAPA.
Soutient les transferts de conception et les transferts d’approvisionnement en collaboration avec les équipes Qualité fournisseurs.
Soutient les enquêtes liées aux plaintes clients.
Works as part of a team, completing Quality tasks in the design and development, and change control processes.
Ensure compliance with global regulations and recognized standards (e.g., FDA 21 CFR Part 820, ISO 13485, ISO 14971, EU MDR).
Review, maintain and approve Design History Files (DHF) and Risk Management Files (RMF).
Identify and mitigate design risks using FMEA and other tools.
Support design verification and validation activities.
Supports design and change control processes.
Collaborate with design teams to embed quality standards.
Author, review and approve documentation in Quality capacity.
Define and control Critical to Quality (CTQ) characteristics.
Assist with regulatory submissions and audits.
Analyze quality data to identify trends and improvement areas.
Support quality improvement initiatives.
Support root cause investigations and CAPA activities.
Supports design transfer and sourcing transfers with Supplier Quality counterparts.
Supports customer complaints investigations.

What Makes You Stand Out

Expérience en contrôles de conception ainsi qu’en vérification et validation (conception, processus et logiciels).
Connaissance pratique de la FDA 21 CFR 820.30, de l’ISO 13485 et du RDM de l’Union européenne.
Compréhension de la gestion des risques (ISO 14971, AMDEC/FMEA et outils statistiques).
Capacité à planifier et à exécuter des activités de V&V, y compris des études sur les facteurs humains et l’utilisabilité.
Maîtrise de l’analyse statistique des données.
Excellentes aptitudes à communiquer dans un environnement multidisciplinaire.
Excellentes compétences en rédaction technique.
Compétences en systèmes informatiques (atouts).

Windchill
Codebeamer
Jira
Microsoft Office
Minitab

Experience in design controls, verification, validation (design, process and software).
Working knowledge of FDA 21 CFR 820.30, ISO 13485, and EU MDR.
Understanding of risk management (ISO 14971, FMEA, statistical tools).
Capable in V&V planning and execution including human factors usability studies.
Proficient in statistical data analysis.
Effective cross-functional communicator.
Excellent technical writing skills.
IT System Skills (Preferred Skills)

Windchill
Codebeamer
Jira
Microsoft Office
Minitab

Your Background

Baccalauréat en génie ou dans un domaine connexe.
Solide compréhension des principes d’ingénierie.
Ceinture jaune ou ceinture verte Six Sigma, un atout.
B.S. in Engineering or related field
Solid foundation in engineering principles
Six Sigma Yellow or Green Belt Preferred

Travel Expectations

Jusqu’à 20 % de déplacements.

Up to 20%

EOE/M/F/Vet/Disability

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More about this job

Responsibilities

Supports quality activities throughout product design, development, change control, and the product lifecycle, ensuring compliance with applicable regulations and standards. Maintains design and risk management documentation, supports verification and validation, audits, regulatory submissions, investigations, CAPA, quality improvement, and design transfers.

Requirements

Requires a bachelor's degree in engineering or a related field and a solid foundation in engineering principles. Desired qualifications include experience with design controls and verification and validation, knowledge of FDA, ISO 13485, ISO 14971, and EU MDR requirements, statistical analysis skills, strong technical writing and communication, and preferably a Six Sigma Yellow or Green Belt.

Skills

Design Controls
Design Verification and Validation
Process Verification and Validation
Software Verification and Validation
Regulatory Compliance
Risk Management
FMEA
Statistical Data Analysis
Human Factors and Usability
Technical Writing
Cross-Functional Communication
Root Cause Investigation
CAPA
Quality Data Analysis
Design Transfer
Change Control

Benefits

Employee Resource Groups
Flexible Working Environment
Competitive Total Rewards
Wellness Incentives
Recognition and Performance Awards

Visa sponsorship

Not detected in the job text

Keywords

FDA 21 CFR Part 820
FDA 21 CFR 820.30
ISO 13485
ISO 14971
EU MDR
Design History File
Risk Management File
FMEA
Design Controls
Design Verification
Design Validation
Process Validation
Software Validation
Human Factors
Usability Studies
Critical to Quality Characteristics
Regulatory Submissions
Audits
Statistical Analysis
Root Cause Analysis
CAPA
Design Transfer
Supplier Quality
Customer Complaints
Six Sigma
Windchill
Codebeamer
Jira
Microsoft Office
Minitab

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