Jobs in Canada

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Added 13 mins ago
LC
Beauty Specialist, Hourly Part Time Flexible Shifts
Loblaw Companies Limited
Calgary, AB
- Part-time
Each store has an Associate-Owner, so you will work for a local business owner while having the support of a national brand. Benefit from a purchase discount program, flexible and varied…
Added 13 mins ago
TH
Tool Rental Associate Part Time - 7245 Regina Northwest
The Home Depot Canada
Regina, SK
- Part-time
Added 13 mins ago
TH
Merchandising Execution Associate Part-Time - 7086 Winnipeg Southwest
The Home Depot Canada
Winnipeg, MB
- Part-time
Added 13 mins ago
TH
Paint Sales Associate Full-Time - 7056 Crossroads
The Home Depot Canada
Winnipeg, MB
- Full-time
Added 13 mins ago
TH
Lumber Associate Part Time (KANATA)
The Home Depot Canada
Ottawa, ON
- Part-time
Added 13 mins ago
TH
Plumbing and Electrical Sales Associate Part Time - 7038 Brandon
The Home Depot Canada
Brandon, MB
- Part-time
Added 13 mins ago
TH
Lumber Sales Associate : Part Time - MARLBOROUGH
The Home Depot Canada
Calgary, AB
- Part-time
Added 13 mins ago
TH
Cashier Part Time - 7038 Brandon
The Home Depot Canada
Brandon, MB
- Part-time
…the assisted check-outs throughout the store. The front end associate will excel at processing transactions accurately and timely by executing our GET checkout…
Added 13 mins ago
TH
Seasonal Sales Associate : Part Time - MARLBOROUGH
The Home Depot Canada
Calgary, AB
- Part-time
Added 13 mins ago
TH
Cashier : Part Time - CHINOOK
The Home Depot Canada
Calgary, AB
- Part-time
…the assisted check-outs throughout the store. The front end associate will excel at processing transactions accurately and timely by executing our GET checkout…
Added 13 mins ago
TH
Lumber Sales Associate : Part Time - RICHMOND
The Home Depot Canada
Richmond, BC
- Part-time
Added 13 mins ago
GF
Warehouse Associate - Nights
Gordon Food Service - Canada
Delta, BC
- Full-time
Ensuring compliance with all Health and Safety rules and regulations and Food Safety programs
Added 13 mins ago
TH
Millwork Sales Associate Part-Time - 7258 Lloydminster
The Home Depot Canada
Lloydminster, AB
- Part-time
Added 28 mins ago
SC
Sales Associate-Print&Services
Staples Canada
Chatham-Kent, ON · Chatham, ON
- Part-time
Added 58 mins ago
M
Associate Director, Clinical Data Management
Merck
Canada
- Full-time
The Associate Director, Data Collection Data Steward, Global Data Management and Standards (GDMS), Global Clinical Data Standards (GCDS) provides program-level oversight of data standards,…
Added 58 mins ago
PC
Payroll Associate (Contract)
Pwc Canada
Toronto, ON
- Full-time
…calculating wages, deductions, and taxes, as well as confirming compliance with relevant laws and regulations. Your responsibilities include collaborating with HR teams to maintain employee…
Added 1 hour ago
A
Associate, Multi-Unit Financing
ATB
Calgary, AB · Edmonton, AB
- Full-time
Ready to help shape Alberta’s multi-family landscape? As an Associate, Multi-Unit Financing, you will be an integral member of the ATB Commercial Real Estate team, directly supporting…
Added 1 hour ago
SD
Pharmacy Assistant, Hourly Part Time Flexible Shifts
Shoppers Drug Mart
Sherwood Park, AB
- Part-time
Each store has an Associate-Owner, so you will work for a local business owner while having the support of a national brand. Benefit from a purchase discount program, flexible and varied…
Added 2 hours ago
W
(CAN) People Greeter
Walmart
Spruce Grove, AB
- Part-time
Added 2 hours ago
W
Associate Technical Consultant, Environmental Scientist
Worley
Calgary, AB
- Full-time
Interpreting environmental data and developing practical, technically sound recommendations that support risk management and regulatory compliance.
Added 2 hours ago
M
Senior Data Center Technician
Microsoft
Quebec, QC
- $73,200 to $119,600 CAD / year
- Full-time
Added 2 hours ago
S
DCN HR Administrator
SLB
Calgary, AB
- Full-time
Conduct periodic audits of HR files and training databases to ensure compliance and completeness.
Added 2 hours ago
TH
Tool Rental Associate Part Time - 7245 Regina Northwest
The Home Depot
Regina, SK
- Part-time
Added 2 hours ago
H
Office Coordinator
hireVouch
Toronto, ON
- Contract
Sustainability: Implement sustainability initiatives in the office under direction. Track and report on sustainability metrics and compliance with environmental regulations under direction.
Added 2 hours ago
GT
Senior Associate, Audit – Relocate to Australia
Grant Thornton Australia
Toronto, ON
- Full-time
Are you an experienced Auditor looking for a role in Australia? We have an exciting opportunity for a Senior Associate to join our Audit team in Melbourne or Adelaide!

Quantum Management Services Ltd.

Quality Assurance Associate

Brantford, ON, Canada

$30 CAD / hour · Contract

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Job details

Pay: $30 CAD / hour
Job type: Contract
Apply by: Nov 29, 2026
Posting language: English
Posted: Oct 30, 2026

Original job description

Position: Quality Assurance Associate
Location: Brantford, ON (On-site)
Salary: $30/hour
Job Type: 6-month Contract - Potential for Extension
Posting Type: Open Vacancy

Do you have a passion for quality, an eye for detail, and experience working in a regulated manufacturing environment? Here's your opportunity to put your expertise to work!

Our client is looking for a Quality Assurance Associate to join their team in Brantford. This role is ideal for a quality professional with pharmaceutical, radiopharmaceutical, or medical-device experience who enjoys solving problems, strengthening quality processes, and ensuring documentation and procedures meet regulatory standards.

You'll play an important role in maintaining quality systems, supporting investigations, and working alongside Quality Control, Quality Assurance, and Manufacturing teams to help keep operations compliant and products up to standard. If you're looking to build on your GMP experience and expand your knowledge of quality systems, this could be an excellent next step.

What's in It for You?

- $30/hour with potential for contract extension
- Hands-on experience in a regulated manufacturing environment
- Exposure to pharmaceutical GMP or medical-device quality systems
- Opportunity to work with deviations, investigations, CAPA, and change control
- Experience using electronic quality systems and controlled documentation
- Collaboration with Quality and Manufacturing teams

Key Responsibilities:

- Review and maintain controlled quality documentation, including SOPs, batch records, forms, logbooks, and other quality records.
- Support deviation and non-conformance investigations by gathering evidence, reviewing documentation, identifying potential root causes, and preparing reports.
- Assist with CAPA activities, including documenting corrective actions, tracking implementation, and supporting follow-up.
- Support change control processes and maintain accurate quality records.
- Ensure documentation meets Good Documentation Practices (GDocP) and applicable GMP requirements.
- Maintain and update quality records using electronic quality management systems (eQMS).
- Support internal audits, regulatory inspections, and audit-readiness activities.
- Assist with product quality reviews, batch documentation review, and release-related activities as required.
- Collaborate with Quality Control, Manufacturing, and other departments to address quality issues and support timely resolution.
- Track quality data, maintain compliance records, and contribute to continuous improvement initiatives.

Qualifications & Experience:

- Experience in a pharmaceutical, radiopharmaceutical, medical-device, or similarly regulated manufacturing environment.
- Working knowledge of GMP requirements, preferably Canadian drug GMP or equivalent FDA drug GMP.
- Experience supporting deviations, investigations, CAPA, and quality documentation.
- Familiarity with Good Documentation Practices (GDocP), SOPs, and controlled records.
- Experience using an eQMS or electronic quality system, such as TrackWise, MasterControl, QT9, or a similar platform.
- Exposure to change control, batch record review, product release, and audit support is an asset.
- Experience with ISO 13485 and/or MDSAP is an asset.
- Laboratory or analytical testing experience with techniques such as HPLC, GC, IR, or titration is an asset but not required.
- Strong attention to detail, documentation, organization, and problem-solving skills.
- Ability to work collaboratively with Quality and Manufacturing teams in an on-site environment.
- Diploma or degree in Science, Chemistry, Life Sciences, Pharmaceutical Sciences, Quality Assurance, or a related field.

PLEASE NOTE THAT APPLICANTS WHO APPLY DIRECTLY TO THE POSTING WILL BE REVIEWED!

REFER A TEMP HIRE AND EARN A BONUS! For details, click here.

All applications are reviewed by our recruitment team, and hiring decisions are made by people. We may also use AI-enabled tools to support parts of the application review process.

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More about this job

Responsibilities

Maintain controlled quality documentation and electronic quality records, and support deviation investigations, CAPA, change control, audits, and batch documentation review. Collaborate with Quality Control, Manufacturing, and other teams to resolve quality issues, maintain compliance, and contribute to continuous improvement.

Requirements

Requires experience in pharmaceutical, radiopharmaceutical, medical-device, or similarly regulated manufacturing, with working knowledge of GMP and experience supporting investigations, CAPA, and quality documentation. A science-related diploma or degree is requested; familiarity with eQMS, change control, batch review, audits, ISO 13485, MDSAP, or laboratory testing is beneficial.

Skills

GMP Compliance
Good Documentation Practices
Quality Documentation
Deviation Investigations
Root Cause Analysis
CAPA
Change Control
Electronic Quality Management Systems
SOP Management
Batch Record Review
Audit Support
Regulatory Inspection Readiness
Product Quality Reviews
Quality Data Tracking
Problem-Solving
Attention To Detail

Benefits

Hands-On Experience In A Regulated Manufacturing Environment
Exposure To Pharmaceutical GMP Or Medical-Device Quality Systems
Opportunity To Work With Deviations, Investigations, CAPA, And Change Control
Experience Using Electronic Quality Systems And Controlled Documentation
Collaboration With Quality And Manufacturing Teams
Potential For Contract Extension

Visa sponsorship

Not detected in the job text

Keywords

Good Manufacturing Practices
Good Documentation Practices
Canadian Drug GMP
FDA Drug GMP
Electronic Quality Management System
TrackWise
MasterControl
QT9
Standard Operating Procedures
Controlled Documentation
Deviation Investigations
Non-Conformance
Root Cause Analysis
Corrective And Preventive Action
Change Control
Batch Records
Product Release
Internal Audits
Regulatory Inspections
Audit Readiness
ISO 13485
MDSAP
HPLC
Gas Chromatography
Infrared Spectroscopy
Titration
Pharmaceutical Manufacturing
Radiopharmaceuticals
Medical Devices
Continuous Improvement

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