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Added 4 mins ago
MM
Manufacturing Engineer
Malach Metal & Machining
Brossard, QC
- Full-time
…operating across Canada and the United States, supporting OEM contract manufacturing and in-house product lines. We take pride in precision, craftsmanship, safety, quality, and teamwork.…
Added 4 mins ago
IC
HR & Admin Generalist - POPJOY Retail
IGG.com Canada
Vancouver, BC
- Full-time
Professional reference check conducted with your consent
Added 4 mins ago
WP
Manager, Safety, Security and Asset Management
Westerner Park
Red Deer, AB
- Full-time
Post-secondary education, professional training or equivalent experience in occupational health and safety, emergency management, security, business continuity, asset management,…
Added 4 mins ago
CE
Class 5 Driver (Construction Equipment)
Cooper Equipment Rentals Limited
Vancouver, BC
- Full-time
We are looking for customer-oriented, motivated individuals to join our professional team.
Added 19 mins ago
B&
Administrative Assistant
Black & McDonald Limited
Toronto, ON · Scarborough, ON
- $47,500 to $57,500 CAD / year
- Full-time
Black & McDonald’s Southern Ontario team is growing! If you are committed and collaborative professional looking to contribute to a hard-working, innovative team, this opportunity is for…
Added 19 mins ago
AC
Chef De Projet Flux De Matériel/ Project Manager (Material Flow)
Aston Carter
Saint-Eustache, QC
- $38 to $45 CAD / hour
- Contract
Ce poste Contract est basé à Saint-Eustache, QC.
Added 19 mins ago
R
Project Engineer
Raise
Saskatoon, SK
- Contract
Contract: Start Date 02/02/2027 to End Date 12/31/2027 (11 Months)
Added 19 mins ago
NC
Assistant, Administration
Newmont Corporation
Dease Lake 9, BC
- $72,700 to $90,900 CAD / year
- Full-time
Whether you are an experienced mining professional or looking to take the next step in your career, Red Chris offers the opportunity to be part of a dynamic team and a significant…
Added 19 mins ago
A
Firmware Engineer
Actalent
Montreal, QC
- $45 to $60 CAD / hour
- Contract
Added 19 mins ago
R
Data Support Engineer
Raise
Burnaby, BC
- Full-time
Contract: Start Date 2026-11-23 End Date 2027-11-26 (1 year)
Added 19 mins ago
N
Application Analyst
NetworkPedia
AB · Edmonton, AB
- Contract
Work Schedule: 36.25 hours per week | 1,210 approved contract hours
Added 19 mins ago
BH
Property Representative 2 (Interconnections and Site C)
BC Hydro
Vancouver, BC
- $104,800 to $112,800 CAD / year
- Full-time
…administering and controlling project implementation elements, contract details, budgets, scope, risks and costs; approving and recommending progress payments and other invoices for payment…
Added 19 mins ago
Project Engineer
Shell
Scotford, AB
Professional Engineer (P. Eng) or must be eligible for accreditation with APEGA in a Professional Engineering capacity
Added 19 mins ago
RS
Sleeman Material Handler
Ryder Supply Chain Solutions
Calgary, AB · CAN - Calgary AB Freeport Blvd
- Full-time
Performing duties within performance measurement guidelines of the contract
Added 19 mins ago
DC
Case Worker - HART Hub - Full-time Contract - 1 Day Vacancy
Durham Community Health Centre
Whitby, ON
- Full-time
Employment Status: Full-time Contract – 1 Day Vacancy
Added 19 mins ago
DC
Case Worker - HART Hub - Full-time Contract - 1 Day Vacancy
Durham Community Health Centre
Oshawa, ON
- Full-time
Employment Status: Full-time Contract – 1 Day Vacancy
Added 19 mins ago
DC
Case Worker - HART Hub - Full-time Contract - 2 Overnight Vacancies
Durham Community Health Centre
Oshawa, ON
- Full-time
Employment Status: Full-time Contract – 2 Overnight Vacancies
Added 19 mins ago
DC
Case Worker - HART Hub - Full-time Contract - 2 Overnight Vacancies
Durham Community Health Centre
Whitby, ON
- Full-time
Employment Status: Full-time Contract – 2 Overnight Vacancies
Added 19 mins ago
DC
Case Worker - HART Hub Full-time Contract - 2 Evening Vacancies
Durham Community Health Centre
Whitby, ON
- Full-time
Employment Status: Full-time Contract – 1 Day Vacancy
Added 19 mins ago
DC
Case Worker - HART Hub Full-time Contract - 2 Evening Vacancies
Durham Community Health Centre
Oshawa, ON
- Full-time
Employment Status: Full-time Contract – 1 Day Vacancy
Added 19 mins ago
B
VP Sales Lead
BMO
Toronto, ON · FCP
- Full-time
Bachelor's degree in Business, Finance, Accounting, Economics, or a related field; advanced degree or professional designation considered an asset.
Added 19 mins ago
B
VP Sales Lead
BMO
Edmonton, AB · Enbridge
- Full-time
Bachelor's degree in Business, Finance, Accounting, Economics, or a related field; advanced degree or professional designation considered an asset.
Added 19 mins ago
R&
IT Project Manager – MPW Replat
Robertson & Company Ltd.
Waterloo, ON
- Contract
How to Apply: If you are a motivated professional looking to contribute to a leading team, please submit your resume outlining your qualifications and experience relevant to this role.…
Added 19 mins ago
MH
Director, Equipment Planning and Biomedical Services
Mackenzie Health
Richmond Hill, ON
- $137,748 to $175,793 CAD / year
- Full-time
…(DBFP) equipment relationships, Managed Equipment Services (MES) contract, as well as a traditional in-house biomedical engineering service and support model. This role also works closely…
Added 19 mins ago
AW
Training and Development Specialist
Agilus Work Solutions
Calgary, AB
- Contract
…across multiple Oil Sands sites in Alberta. This fly-in-fly-out contract opportunity is ideal for a training and competency professional who thrives in field-based industrial environments…

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!

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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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