Full-time jobs in Canada (393,844 jobs)

Explore full-time jobs across Canada. Choose a location and read the full job details.

393,844 listings · 47,927 employers Counted Nov 12, 2026. How we count

About these jobs

Employers hiring include Walmart Canada (9,455 listings), Health Match BC (4,294 listings), Walmart (3,010 listings).

Common roles: Project manager, Sales representative, Cook.

68,330 of these listings include employer-provided pay. Open a job to see its currency and pay period.

Advertised starting pay
Pay period	Median starting pay	Listings
CAD / hour	24.00	39,518
CAD / year	80,000.00	26,437
CAD / month	5,377.61	715
USD / year	126,000.00	230
CAD / week	1,622.80	83
CAD / day	360.00	44
USD / hour	22.00	29
GBP / year	40,000.00	13
EUR / year	68,000.00	11
USD / month	4,000.00	11

Employer-listed minimums from at least 10 listings per currency and pay period. These are advertised starting amounts, not employee salaries. Jobs without a minimum and unusual amounts are excluded.

Workplace classifications: 1% remote, 16% hybrid, 82% on-site, 0% not specified. Hybrid and on-site classifications may be inferred from descriptions. Check the original ad.

Based on the dated count above. Listings can change. How we count

Full-time jobs in Canada

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Added 1 hour ago
YO
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Kelowna, BC · Lake Country, BC
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Must Have(s)
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Dillon Consulting Limited
Calgary, AB · Winnipeg, MB · Saint John, NB · Fredericton, NB · Moncton, NB · Yellowknife, NT · Sydney Indian Reserve No. 28A, NS · Halifax, NS · St. John's, NL · Edmonton, AB · Sydney, NS
- Full-time
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Senior Corporate Communications Specialist
Dillon Consulting Limited
Hamilton, ON · Guelph, ON · Kingston, ON · London, ON · Toronto, ON · Ottawa, ON · Oakville, ON · Kitchener, ON · Vancouver, BC · Chatham-Kent, ON · North York, ON · Chatham, ON
- Full-time
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Toronto, ON
- Full-time
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Ottawa, ON
- Full-time
This position is a hybrid position with a minimum – 3 days per week on site
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Calgary, AB
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Spruce Grove, AB
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All applicants must have legal authorization to work in the country where the position is based, without restricti
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framing manager
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Peterborough, ON
- Full-time
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Welland, ON
- Full-time
Full Time Day shift Supervisor
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Toronto, ON
- Full-time
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Winnipeg, MB
Journeyman / Red Seal Automotive Service Technician certification required
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Machinist Granton, NS
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New Glasgow, NS
- Full-time
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Waste Connections of Canada
Fort St. John, BC
- Full-time
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- Full-time
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Toronto, ON · Sun Life Toronto One York
- Full-time
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Sr Risk Analyst
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Calgary, AB
- Full-time
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Armour Transportation Systems
St. John's, NL
- Full-time
Day Shift Available | Steady Year-Round Work | Flexible Schedules · We're hiring Class 1 Drivers (P&D) for opportunities across Grand Falls and St.John's NL for day shifts and local work
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Lumsden, SK
- $20 to $25 CAD / hour
- Full-time

DPS Group Global

Process Engineer (CQV)

Lunenburg, NS, Canada

Full-time

Apply on LinkedIn About employer

Applications open in a new tab.

Job details

Job type: Full-time
Apply by: Nov 20, 2026
Experience: Minimum 5 years' experience in Commissioning, Qualification and Validation (CQV) within a regulated pharmaceutical environment.
Posting language: English
Posted: Nov 12, 2026

Original job description

Overview

Our Client is seeking a Process Engineer to support capital projects on site, providing technical oversight of Commissioning, Qualification and Validation (CQV) activities. The successful candidate will ensure process requirements, GMP principles and risk-based methodologies are appropriately applied throughout project delivery, maintaining compliance and inspection readiness.

Key Responsibilities

Provide technical oversight and review of CQV documentation, including commissioning plans, risk assessments, qualification protocols and reports.
Ensure process requirements are effectively translated into GMP-compliant design and qualification strategies.
Support the identification, justification and control of critical quality attributes (CQAs) and critical process parameters (CPPs).
Apply risk-based approaches to determine qualification scope, testing requirements and verification activities.
Review and approve CQV strategies, plans and lifecycle documentation.
Challenge and guide project teams, vendors and CQV service providers to ensure regulatory and industry best practice compliance.
Support design reviews, change controls and deviation investigations from a technical compliance perspective.
Ensure systems remain in a validated state and support ongoing inspection readiness.

Requirements

Bachelor's degree in Engineering (Chemical, Mechanical, Electrical or related discipline).
Minimum 5 years' experience in Commissioning, Qualification and Validation (CQV) within a regulated pharmaceutical environment.
Strong understanding of pharmaceutical manufacturing processes, CQAs and CPPs.
Working knowledge of GMP regulations and industry standards, including EU GMP, FDA and ICH guidelines.
Experience reviewing and approving CQV lifecycle documentation.
Strong risk assessment, problem-solving and analytical skills.
Excellent stakeholder management and communication abilities.
Ability to identify, assess and escalate compliance and quality risks.

Apply on LinkedIn About employer

More about this job

Responsibilities

Provide technical oversight and review of CQV strategies, plans, risk assessments, qualification protocols, reports, and lifecycle documentation for capital projects. Ensure process requirements and risk-based approaches are applied in GMP-compliant design and qualification, while supporting change controls, deviation investigations, validated-state maintenance, and inspection readiness.

Requirements

Requires a bachelor's degree in engineering and at least five years of CQV experience in a regulated pharmaceutical environment. Candidates should understand pharmaceutical manufacturing, CQAs and CPPs, GMP regulations and EU GMP, FDA, and ICH guidance, and have strong documentation review, risk assessment, problem-solving, analytical, and stakeholder communication skills.

Skills

Commissioning, Qualification, And Validation (CQV)
GMP Compliance
Pharmaceutical Manufacturing Processes
Critical Quality Attributes (CQAs)
Critical Process Parameters (CPPs)
Risk Assessment
CQV Documentation Review
Qualification Protocols
Design Reviews
Change Control
Deviation Investigations
Stakeholder Management
Problem-Solving
Analytical Skills
Inspection Readiness

Visa sponsorship

Not detected in the job text

Keywords

Commissioning, Qualification, And Validation (CQV)
Good Manufacturing Practice (GMP)
EU GMP
FDA Guidelines
ICH Guidelines
Pharmaceutical Manufacturing
Capital Projects
Process Requirements
Critical Quality Attributes (CQAs)
Critical Process Parameters (CPPs)
Risk-Based Methodologies
Risk Assessments
Qualification Protocols
Commissioning Plans
CQV Strategies
Lifecycle Documentation
GMP-Compliant Design
Design Reviews
Change Control
Deviation Investigations
Validated State
Inspection Readiness
Regulatory Compliance
Quality Risk Management

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Work requirements

Full-time jobs in Canada