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Added 29 mins ago
LC
Senior Manager, Pensions
Loblaw Companies Limited
Toronto, ON
- Full-time
Support the Director of Pensions & Savings in the governance, financial risk management and overall pension and savings strategy for several registered defined benefit pension plans,…
Added 1 hour ago
W
(CAN) Manager, Business Operations eCommerce
Walmart
Mississauga, ON
- Full-time
Operational planning focuses on supply needs, with the manager developing incentives to optimize resource efficiency. The manager collaborates with stakeholders to drive program expansion…
Added 1 hour ago
S
Senior Environmental Coordinator
Stelco
Hamilton, ON
- Full-time
…monitoring contractor/vendor safety in support of work efforts. This senior-level role will take ownership of environmental projects and programs from planning through to completion and is…
Added 2 hours ago
LD
Manager of Facility Services & Capital Asset Management
Limestone District School Board
Kingston, ON
- Full-time
Reporting to the Superintendent of Business Services, the Manager will provide strategic leadership and operational oversight for the Board's facility services and capital asset management…
Added 2 hours ago
UO
Senior Manager, Animal Care Operations
University of Ottawa
Ottawa, ON
- Full-time
The Senior Manager leads managers and supervisors responsible for the operational delivery of animal care and research support services across the University's animal care facilities. The…
Added 2 hours ago
MP
Senior Manager - Estimating (Mining)
Michael Page
Toronto, ON · Greater Toronto Area, Canada
- $180,000 to $195,000 CAD / year
- Full-time
As a Senior Manager - Estimating, you will lead the development and delivery of major capital mining projects. You will provide estimating leadership across all project phases, ensuring…
Added 2 hours ago
Team Lead, Talent Acquisition (Civil)
Aecon
Toronto, ON
Reporting to the Senior Talent Acquisition Manager – Civil, the Team Lead will provide day-to-day leadership, mentorship and operational support to members of the Civil Talent Acquisition…
Added 3 hours ago
AC
Finance Manager, Academic
Algonquin College
Ottawa, ON
- Full-time
…Accepted Accounting Principles, internal financial controls and operational procedures within the Academic Area and ensures that financial and operational reconciliations and reports are…
Added 3 hours ago
SB
Senior Buyer
Steelway Building Systems
Aylmer, ON
- Full-time
The Senior Buyer must be comfortable analyzing complex information, identifying supply chain risks, challenging existing sourcing practices, and developing practical solutions that support…
Added 3 hours ago
I|
Manager - Logistics Technology SecOps
Intelcom | Dragonfly
Montreal, QC
- Full-time
Work with operations teams to reduce risk without slowing the delivery network.
Added 3 hours ago
MI
Senior Manager, Fund Accounting, Private Markets
MUFG Investor Services
Vancouver, BC
- $105,000 to $154,000 CAD / year
- Full-time
The Senior Associate Director is accountable for the performance and results of assigned private equity and private debt client portfolios, ensuring high-quality, timely and controlled…
Added 3 hours ago
M
Senior Manager, Project Controls
Metrolinx
Canada
- Full-time
This role requires you to be on-site at the office, 5 days per week
Added 4 hours ago
A
Sales Excellence and Planning Manager
Altis
Toronto, ON
- $150,000 to $160,000 CAD / year
- Full-time
This opportunity offers a balance of operational leadership and project delivery. You'll collaborate with Canadian and global teams, strengthen client servicing processes, and help…
Added 4 hours ago
PC
Manager, Internal Controls and Risk Management – Financial Services (Bilingual FR/EN)
PwC Canada
Montreal, QC
- Full-time
As a Manager, Internal Controls and Risk Management – Financial Services, you will work with a team of professionals to help anticipate and solve internal control and risk management…
Added 4 hours ago
Senior Project Manager (Contract)
Blue Ant Media Inc.
Toronto, ON
The Senior Project Manager leads the planning and delivery of technology and business transformation initiatives across Blue Ant Media, with accountability for project outcomes from initial…
Added 4 hours ago
QT
Manager, Project Management Office (PMO)
Quantum Technology Recruiting Inc. (QTR)
Toronto, ON
- $160,000 to $170,000 CAD / year
- Full-time
Working Model: Onsite - 4 days per week currently, moving to 5 days onsite downtown
Added 4 hours ago
FA
Commodity Manager – CFM56 Engine Components
FTAI Aviation
Montreal, QC
- Full-time
Reporting to the Senior Vice President, Supply Chain, you will lead end‑to‑end commodity strategy, from demand planning and sourcing to supplier development, contract negotiations, and risk…
Added 4 hours ago
Network Engineer-GCGCON
Great Canadian Entertainment
Toronto, ON · North York, ON
Under the general direction of Sr Manager, Network Services & Delivery, the Network Engineer is a senior level hands on technical leader responsible for the architecture, design,…
Added 4 hours ago
P
Manager, Internal Controls and Risk Management – Financial Services (Bilingual FR/EN)
PwC
Montreal, QC
- Full-time
As a Manager, Internal Controls and Risk Management – Financial Services, you will work with a team of professionals to help anticipate and solve internal control and risk management…
Added 5 hours ago
UC
Senior AI Project Manager
UniSysTech Consulting
Toronto, ON · Greater Toronto Area, Canada
- Other
We are seeking an experienced Senior Project Manager – AI SDLC to lead the strategic rollout of enterprise-wide, AI-augmented engineering capabilities, developer tooling, and intelligent…
Added 5 hours ago
WP
Sr. Project Manager
Western Pacific Enterprises LTD
AB · Edmonton, AB
- Full-time
WPE is seeking a highly experienced Senior Project Manager to lead and oversee the delivery of assigned Power and Systems work packages on the Capital Line South Extension project in…
Added 5 hours ago
I
Manager - Logistics Technology SecOps
Intelcom
Montreal, QC · Service Centre (Montreal) Lab
- Full-time
Work with operations teams to reduce risk without slowing the delivery network.
Added 5 hours ago
IR
Associate Vice President, Salesforce Engineering & Development
Info-Tech Research Group
Toronto, ON · London, ON
- Full-time
…a Quality Engineering Lead, and a Salesforce Administration Manager, all while partnering as a peer with Product Management and collaborating closely with a separate Architecture…
Added 6 hours ago
FC
Chargé de projet TI
FOP Consultants
Montreal, QC
- Full-time
FOP CONSULTANTS is looking for a motivated Senior IT Project Manager to contribute to the successful delivery of projects. Key responsibilities include end-to-end management of large-scale…
Added 6 hours ago
E
Senior Manager, Program Transformation and Service Excellence
Eva's
Toronto, ON
- $84,241 to $97,760 CAD / year
- Full-time
Senior Manager, Program Transformation and Service Excellence is responsible for leading strategic initiatives, quality improvement activities, service excellence projects, program…

VitalBio

Senior Quality Management System (QMS) Quality Engineer

400 Iroquois Shore Rd, Oakville, ON, L6H 1M5, Canada

The compensation range for this role is $90,000-$115,000. · Full-time

Apply on vitalbio.na.teamtailor.com About employer

Applications open in a new tab.

Job details

Pay: The compensation range for this role is $90,000-$115,000.
Job type: Full-time
Experience: Minimum 7 years of Quality Engineering or Quality Systems experience within a regulated medical device environment.
Posting language: English
Posted: Oct 6, 2026

Original job description

Position Summary

The Senior Quality Management System (QMS) Quality Engineer is a technical leader responsible for maintaining, improving, and ensuring the effectiveness of the Company's Quality Management System (QMS) and electronic Quality Management System (eQMS). This individual partners closely with Quality, Regulatory Affairs, R&D, Manufacturing, Operations, Supply Chain, and Program Management to ensure compliance with applicable regulatory requirements and industry standards throughout the product lifecycle.

The Senior QMS Quality Engineer will lead quality system initiatives including CAPA, change control, document control, training, audits, supplier quality, management review, risk management, and continuous improvement activities. This role will serve as a key quality systems resource supporting product development, verification, validation, commercialization, and post-market activities within a regulated medical device environment.

Diagnostics, point-of-care diagnostics, molecular diagnostics, or IVD experience is strongly preferred.

Key Responsibilities

Quality Management System Leadership

Maintain and continuously improve the Quality Management System (QMS) in accordance with applicable regulatory requirements and industry standards.
Ensure compliance with FDA QMSR, ISO 13485, ISO 14971, MDSAP, Health Canada Medical Device Regulations, and internal procedures.
Support development, implementation, and continuous improvement of quality policies, procedures, and processes.
Monitor quality system performance and identify opportunities for improvement.
Support organizational readiness for regulatory inspections, certification audits, and commercialization activities.

eQMS Administration & Process Ownership

Serve as a primary administrator and business process owner for the electronic Quality Management System (eQMS).
Configure and maintain workflows associated with document control, training, CAPA, nonconformance, change control, complaints, supplier quality, and audits.
Support eQMS implementations, upgrades, enhancements, validation activities, and data migrations.
Develop reports, dashboards, and metrics to monitor quality system effectiveness.
Partner with IT and software vendors to maintain compliant and efficient system functionality.
Drive user adoption and continuous improvement of eQMS capabilities.

CAPA, Nonconformance & Change Control

Lead and facilitate CAPA, nonconformance, deviation, and change control processes.
Conduct and support root cause investigations using structured problem-solving methodologies.
Ensure corrective and preventive actions are appropriately implemented and verified for effectiveness.
Monitor quality system trends and identify systemic improvement opportunities.

Audit & Inspection Readiness

Plan, conduct, and support internal audits.
Participate in supplier audits, customer audits, certification audits, and regulatory inspections.
Manage audit findings and ensure timely closure of corrective actions.
Maintain a state of continuous audit readiness across the organization.

Document Control & Training

Support document lifecycle management including creation, review, approval, revision, and archival.
Ensure training requirements are established and maintained.
Monitor training compliance and effectiveness.
Support development and maintenance of quality system documentation and records.

Product Development & Risk Management Support

Support design control activities throughout product development.
Participate in design reviews, verification, validation, and design transfer activities.
Support implementation and maintenance of risk management processes in accordance with ISO 14971.
Review design and process changes for quality system and regulatory impact.

Supplier Quality Support

Support supplier qualification, monitoring, and re-evaluation activities.
Participate in supplier audits and supplier corrective action activities.
Support supplier performance monitoring and quality agreements.
Ensure supplier quality processes align with company quality requirements.

Management Review & Quality Metrics

Support Management Review preparation and execution.
Develop and maintain quality system performance metrics and dashboards.
Analyze trends and recommend quality system improvements.
Present quality system performance data to leadership teams as required.

Continuous Improvement

Lead and support quality system improvement initiatives.
Drive simplification, harmonization, and optimization of quality processes.
Apply risk-based decision making to quality system improvements.
Promote a culture of quality and continuous improvement across the organization.

Qualifications

Education

Bachelor's degree in Engineering, Biomedical Engineering, Life Sciences, Quality, or a related technical discipline.

Experience

Minimum 7 years of Quality Engineering or Quality Systems experience within a regulated medical device environment.
Minimum 5 years supporting and maintaining Quality Management Systems compliant with ISO 13485 and FDA requirements.
Demonstrated experience administering and maintaining electronic Quality Management Systems (eQMS).
Experience supporting FDA inspections, MDSAP audits, ISO 13485 certification audits, and customer audits.
Experience supporting product development, design controls, verification, validation, and commercialization activities.
Diagnostics, IVD, point-of-care diagnostics, molecular diagnostics, or laboratory instrumentation experience strongly preferred.

Required Technical Expertise

Quality Management Systems (QMS)
Electronic Quality Management Systems (eQMS)
ISO 13485
FDA Quality Management System Regulation (QMSR)
MDSAP
Health Canada Medical Device Regulations
ISO 14971 Risk Management
CAPA, Nonconformance, Deviation, and Change Control Systems
Internal Auditing and Audit Management
Document Control and Training Systems
Supplier Quality Management
Design Controls and Product Development Processes
Root Cause Analysis and Corrective Action Methodologies
Data Integrity Principles (ALCOA+)
Quality Metrics, Reporting, and Dashboard Development
Computer System Validation (CSV)

Preferred eQMS Experience

Experience with one or more of the following:

MasterControl
Greenlight Guru
Veeva
ETQ Reliance
TrackWise
Arena QMS
Equivalent regulated eQMS platforms

Preferred Certifications

ASQ Certified Quality Engineer (CQE)
ASQ Certified Quality Auditor (CQA)
ASQ Certified Manager of Quality/Organizational Excellence (CMQ/OE)
ISO 13485 Lead Auditor
Lean Six Sigma Green Belt or Black Belt
Regulatory Affairs Certification (RAC)

Success Measures

Effective maintenance and continuous improvement of the Quality Management System.
Successful completion of external audits, certification audits, and regulatory inspections.
Timely and effective closure of CAPAs, nonconformances, and change controls.
High levels of document control and training compliance.
Effective utilization and continuous improvement of the eQMS platform.
Successful support of product development, verification, validation, and commercialization activities.
Continuous improvement in quality system effectiveness, compliance, and operational efficiency.
Strong cross-functional partnerships supporting organizational quality objective

Why join us:

At Vital Bio, you will:

Drive sourcing strategies that directly impact the delivery and quality of cutting-edge diagnostic products.
Work with a diverse, high-performing team dedicated to innovation, operational excellence, and patient impact.
Grow your expertise and career in a supportive, fast-paced setting.
Be part of a company that values your insight, adaptability, and sense of humor.

The compensation range for this role is $90,000-$115,000. Compensation will be determined based on the individual’s demonstrated experience, education, training, relevant certifications or licensure, and other applicable business and organizational factors.

This role is a current, onsite vacancy.

About Vital

Vital is revolutionizing point-of-care diagnostics with our VitalOne platform, delivering real-time care wherever patients are. Our mission is to democratize health technology, making healthcare more accessible and proactive.

Our global team of experts spans chemistry, software, engineering, and microfluidics. We thrive on change, operate on trust, and value diverse perspectives. Our growth-minded culture empowers front-line decision-making and fosters impactful work.

We seek tenacious, bold individuals ready to transform healthcare. At Vital, your talent will make a difference as we work to ensure everyone has access to care when and where they need it.

Join us in revolutionizing healthcare and making a lasting impact on people's lives.

Vital Biosciences Inc. is an equal opportunity employer and values diversity in the workplace. We are therefore happy to accommodate any individual needs in keeping with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act. If you require accommodation in order to participate in our hiring process, please contact us to make your needs known in advance.

Apply on vitalbio.na.teamtailor.com About employer

More about this job

Responsibilities

The Senior QMS Quality Engineer is responsible for maintaining and improving the company's Quality Management System and electronic QMS to ensure regulatory compliance. This role leads key quality initiatives including CAPA, audits, risk management, and supplier quality while supporting product development and commercialization.

Requirements

Candidates must hold a bachelor's degree in Engineering, Life Sciences, or a related field and possess at least 7 years of experience in a regulated medical device environment. Strong expertise in ISO 13485, FDA regulations, and eQMS administration is required, with preference given to those with diagnostics or IVD industry experience.

Skills

Quality Management Systems
eQMS Administration
ISO 13485
FDA QMSR
CAPA
Change Control
Risk Management
ISO 14971
Internal Auditing
Document Control
Supplier Quality Management
Design Controls
Root Cause Analysis
Data Integrity
Quality Metrics
Computer System Validation

Visa sponsorship

Not detected in the job text

Keywords

Quality Management System
eQMS
ISO 13485
FDA QMSR
ISO 14971
MDSAP
CAPA
Change Control
Document Control
Risk Management
Supplier Quality
Design Controls
Root Cause Analysis
Data Integrity
Computer System Validation
Medical Device
Diagnostics
IVD
MasterControl
Greenlight Guru
Veeva
ASQ
Lean Six Sigma
Regulatory Affairs
Quality Engineering
Compliance
Auditing
Product Development
Verification
Validation

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Jobs in Canada