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Added 12 mins ago
PH
Founding Engineer
Prometheus Health Systems
Remote, Canada
- $150,000 to $190,000 CAD / year
- Full-time
- Remote
As our first engineer, you'll work directly with the founder, a practising physician who built the platform, and with our clinical collaborators. You'll take ownership of a working system…
Added 12 mins ago
S
Test R&D Engineer, Co-Op
Stryker
Burnaby, BC
- Full-time
The Test R&D Engineer, Co-op will work with the Opto-mechanical Test R&D team to ensure we develop high quality products within Stryker Endoscopy’s product portfolio. Test R&D engineers…
Added 27 mins ago
R
SCADA Transmission Engineer
Raise
Burnaby, BC
- Full-time
Demonstrated expertise with GE RTU products (e.g., GE D400, D20, D200, D25, IBOX), Ethernet networks, DNP3 protocol, Modbus Plus® protocol, and protocol test equipment/software.
Added 27 mins ago
P
Senior Software Engineer - Java/React
PointClickCare
Mississauga, ON
- Full-time
Strong track record building and shipping production software in modern languages
Added 27 mins ago
P
Principal Software Engineer
PointClickCare
Mississauga, ON
- Full-time
Strong track record building and shipping production software in modern languages
Added 27 mins ago
B
Jr. Hardware Engineer
Broadcom
Ottawa, ON
- Full-time
Test Execution: Set up and conduct mechanical or electrical tests on prototypes under the direction of the lead engineer.
Added 42 mins ago
IG
Dayforce Application Engineer
Insight Global
Canada
- Contract
Insight Global is seeking a Dayforce Application Engineer to join a large retail client. This individual will join the People Enablement Technology team and support the ongoing health and…
Added 42 mins ago
HT
PD Software for Service
Husky Technologies
Bolton, ON
- Full-time
The Service team is currently seeking a Software engineer/designer to specialize in resolving service issues with a focus on Injection Molding Machine controls, including servo drive and…
Added 42 mins ago
HT
Manufacturing Engineer (Contract)
Husky Technologies
Bolton, ON
- Full-time
We have an opening for a Mechanical / Manufacturing Engineer working with our Manufacturing Engineering Team as outlined below:
Added 42 mins ago
A
Software Engineer
Applicantz
Toronto, ON
- $50 to $55 CAD / hour
- Contract
…Solutions (PDMS) division. We are looking for an experienced Software Engineer to join one of our teams to help us fulfill the mission of the organization, supporting cross-platform device…
Added 42 mins ago
P
Principal Software Engineer
PointClickCare
Mississauga, ON
- $142,700 to $178,400 CAD / year
- Full-time
Strong track record building and shipping production software in modern languages
Added 42 mins ago
P
Senior Software Engineer - Java/React
PointClickCare
Mississauga, ON
- $130,100 to $162,600 CAD / year
- Full-time
Strong track record building and shipping production software in modern languages
Added 42 mins ago
M
Senior Software Engineer-C#
Morningstar
Toronto, ON
- Full-time
Morningstar is seeking a Senior Software Engineer (Backend) to design, build, and maintain scalable enterprise applications and APIs. The role focuses on backend development using C#, .NET,…
Added 56 mins ago
AT
Hardware Engineer Co-op
Arlo Technologies
Richmond, BC · CA - British Columbia - Richmond
- $3,500 to $4,000 CAD / month
- Full-time
…production life cycle development, exposure to a wide variety of test equipment and an introduction to BLE/WiFi technologies. Specifically, you will be responsible for the design of new IoT…
Added 1 hour ago
A
Frontend Software Engineer – React/TypeScript
Applicantz
Toronto, ON
- $50 to $55 CAD / hour
- Contract
…Solutions (PDMS) division. We are looking for an experienced Software Engineer to join one of our teams to help us fulfill the mission of the organization, supporting cross-platform device…
Added 1 hour ago
IC
Python Developer
IT Connex
Toronto, ON · Greater Toronto Area, Canada
- Contract
Design, develop, test, and support Python-based applications and services.
Added 1 hour ago
CG
Embedded Software Test Engineer / HSIT – ISO 26262
CS GROUP
Ottawa, ON
- Full-time
We are looking for a detail-oriented Embedded Software Test / Verification & Validation Engineer to support testing activities within an HSIT team in an automotive environment.
Added 1 hour ago
CD
Lead Digital Verification Engineer
Cadence Design Systems
Montreal, QC
- Full-time
…aspects of digital verification including flow development, test plan development and execution, functional coverage closure, and code coverage…
Added 1 hour ago
FM
Quality Engineer
FluidAI Medical
Kitchener, ON
- $70,000 to $85,000 CAD / year
Create test methods and strategies for existing and new products, backed by sound statistical rationale.
Added 1 hour ago
CT
System Designer Co-Op
Comtech Telecommunications Corp.
Gatineau, QC
- Full-time
- Temporary
- Internship
Integrate, validate, and test complex system features.
Added 1 hour ago
GI
Mechanical Field Engineer
Green Infrastructure Partners
Paradise, NL · St. John's, NL · Topsail Rd, Paradise, NL
- Full-time
…cleaning activities, as applicable. Maintain inspection and test records and track deficiencies and corrective actions with the responsible…
Added 1 hour ago
GI
Electrical Field Engineer
Green Infrastructure Partners
Paradise, NL · St. John's, NL · Topsail Rd, Paradise, NL
- Full-time
…qualified and authorized personnel; maintain inspection and test records and track deficiencies and corrective…
Added 1 hour ago
Senior AI Engineer, IT Solutions 1 1 1
Celestica International LP
Toronto, ON
We are seeking a highly motivated and technically proficient AI Engineer to join our growing Data & Analytics team. In this role, you will be a key liaison between business stakeholders and…
Added 1 hour ago
QW
QA Automation Engineer – Selenium & Playwright
Quantum World Technologies Inc.
Toronto, ON
- Contract
Experience with TestNG, JUnit, or Playwright Test frameworks.
Added 1 hour ago
A
Quality Assurance Tech III
Actalent
Vancouver, BC
- $45 to $50 CAD / hour
- Contract
We are seeking a talented and highly motivated Quality Assurance Engineer for a contract position. The ideal candidate possesses excellent communication skills, attention to detail, and has…

FluidAI Medical

Quality Engineer

Kitchener, ON, Canada

$70,000 to $85,000 CAD / year

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Job details

Pay: $70,000 to $85,000 CAD / year
Experience: 2-5 years of experience working in a medical device or similarly regulated environment.
Posting language: English
Posted: Nov 3, 2026

Original job description

Job Summary:

Do you believe that quality and fast progress can go hand in hand? Do you enjoy solving technical problems in a fast-paced environment? Are you passionate about quality and delivering life-changing medical devices? If so, read on!

At FluidAI, patient safety and regulatory compliance are non-negotiable. We rely on sound judgement and a risk-based approach to meet them effectively, focussing effort where it matters most. You’ll work closely with a cross-functional team to support the development, implementation, and operation of a Quality Management System that is compliant while also being clear, efficient, and scalable. You’ll make sure our controls fit the risk, keep documentation meaningful, and help the team efficiently meet requirements. You’ll also support regulatory activities across Canada, the US, and International markets.

This position requires you to come into our Kitchener, ON office at least 50% of the time.

Job Responsibilities:

Use a risk-based approach to quality. Apply rigor where it matters most, and keep things lean where it doesn't.
Partner with engineering and operations to ensure quality is built into product and processes
Own the linkage of Design Controls in all stages of the production lifecycle.
Ensure product, material, and process specifications are clear, unambiguous, and practical for production.
Create test methods and strategies for existing and new products, backed by sound statistical rationale.
Plan, execute, and analyze test method/process validations.
Lead and support component/product inspection and qualification activities.
Support identification, auditing, and onboarding of new suppliers to ensure compliance and business continuity.
Create and maintain process risk documentation in line with ISO 14971, and evaluate process risks to set appropriate controls throughout the product lifecycle
Lead investigation and timely closure of non-conformances and CAPAs.
Assess engineering change for quality and regulatory impact, and maintain change control in a way that keeps work moving.
Support regulatory submissions, licence applications and amendments, and responses to regulator questions.
Support post-market activities, including complain handling, post-launch monitoring, and trend analysis.
Support the creation of Device Master Records and the transfer of processes to manufacturing
Support internal audits, external audits (ex: MDSAP), and interaction with testing laboratories
Look for ways to simplify and improve the QMS, and challenge processes that add burden without reducing risk
Collaborate with Subject Matter Experts on process validation activities to ensure consistent, repeatable, and effective processes are implemented during design and manufacturing transfer.
Maintain and support the development of process control and monitoring to ensure effective process transfer activities and compliance

Required Qualifications:

Bachelor’s Degree in engineering or a science-related field.
2-5 years of experience working in a medical device or similarly regulated environment.
Working knowledge of ISO13485:2016, ISO 14971, IEC 60601-1:2005, and other relevant standards.
Strong knowledge of Quality Concepts, with the judgement to know where requirements can flex and where they can't.
Comfort making risk-based decisions with incomplete information, and the ability to clearly document and defend your rationale.
Strong analytical skills with practical knowledge of statistical methods.
Strong project management skills and the ability to juggle shifting priorities in a fast-moving environment
Ability to work independently and take ownership.
Collaborative, solutions-oriented mindset. You help the team find practical, compliant solutions instead of simply flagging problems.
Ability to work cross-functionally with departments such as Operations, Product Development, Regulatory Affairs, R&D, and Marketing.
Strong interpersonal, written, oral communication, and negotiation skills.
Familiarity with cGMP.
Experience interacting with regulatory agencies (FDA, Health Canada, etc.) and Auditing Organizations/Testing Laboratories (TUV, Intertek, Nemko, etc.).

Preferred Qualifications:

MASc or MS.
CQE, CRE, or RAC certifications.
Experience preparing or supporting regulatory submissions
Experience interacting with regulators, notified bodies, auditing organizations, and testing laboratories
Experience with MDSAP audits
Thorough knowledge of Canadian, US, and International Medical Device Regulations
Experience assessing changes for regulatory reportability
Familiarity with post-market surveillance, complaint handling, and adverse event reporting
Familiarity with IEC 62304 and software as/in a medical device
Experience building or scaling a QMS at a startup or early-stage company
Familiarity with Six Sigma and/or Lean manufacturing.
Applied knowledge of Advanced Quality tools (FMEA, GD&T, Root Cause Analysis, Mistake Proofing/Poka Yoke).
Experience with the medical device product development lifecycle (risk management, design/process verification, and validation).
Ability to read and interpret CAD drawings.
Experience working in compliance risk situations.
Familiarity with Python or similar programming languages.

Transparency & Hiring Practices:

Compensation: Salary range for this position is $70,000 - $85,000 CAD annually.
Application Screening: All applications are screened manually. We do not use AI or AI-Augmented Applicant Tracking Systems (ATS) to screen, assess, reject, or select candidates.
Position Status: This job posting is for an active vacancy.

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More about this job

Responsibilities

Develop, maintain, and improve a risk-based Quality Management System while ensuring design controls, specifications, validations, supplier quality, and manufacturing processes meet applicable requirements. Lead quality investigations and change control, support regulatory submissions and post-market activities, and contribute to audits and process transfers.

Requirements

Requires a bachelor’s degree in engineering or a science-related field and 2–5 years of experience in medical devices or a similarly regulated environment. Candidates should know ISO 13485, ISO 14971, IEC 60601-1, cGMP, and statistical methods, and be able to make risk-based decisions, manage priorities, and collaborate across functions.

Skills

Risk-Based Quality Management
Design Controls
Quality Management Systems
Process Validation
Statistical Analysis
Supplier Auditing
Risk Management
CAPA
Non-Conformance Investigation
Change Control
Regulatory Submissions
Post-Market Surveillance
Complaint Handling
Internal and External Auditing
Cross-Functional Collaboration
Project Management

Visa sponsorship

Not detected in the job text

Keywords

ISO 13485:2016
ISO 14971
IEC 60601-1
IEC 62304
cGMP
MDSAP
FDA
Health Canada
Quality Management System
Design Controls
Risk Management
FMEA
CAPA
Root Cause Analysis
Process Validation
Test Method Validation
Statistical Methods
Supplier Auditing
Change Control
Regulatory Submissions
Post-Market Surveillance
Complaint Handling
Adverse Event Reporting
Six Sigma
Lean Manufacturing
GD&T
Poka Yoke
Device Master Records
Medical Device Regulations
Python

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