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Quality Associate Jobs in Quebec (NOW HIRING)

Support QC inspectors and QA programs. WHAT WE ARE LOOKING FOR * Secondary 5 or baccalaureate in quality, mechanics, industry or similar discipline; * 5-10 years experience in a similar role ...

The Quality Engineering role designs, implements, and maintains quality assurance methodologies, controls, and inspection protocols to ensure materials and manufacturing processes consistently meet ...

We are looking for an experienced Quality Engineer for our client. This is a permanent position that is remote to start with later relocation to Calgary or Winnipeg . Our client is a global ...

We are looking for an experienced Quality Engineer for our client. This is a permanent position that is remote to start with later relocation to Calgary or Winnipeg . Our client is a global ...

We are looking for an experienced Quality Engineer for our client. This is a permanent position that is remote to start with later relocation to Calgary or Winnipeg . Our client is a global ...

We are looking for an experienced Quality Engineer for our client. This is a permanent position that is remote to start with later relocation to Calgary or Winnipeg . Our client is a global ...

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Quality Associate information

See Quebec salary details

$10

$20

$31

How much do quality associate jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for quality associate in Quebec is $20.75, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $24.04 per hour, depending on experience, location, and employer.

What Does a Quality Associate Do?

A quality associate works as part of a team, typically in the manufacturing industry, to inspect and audit a factory to ensure that production follows the necessary protocols and delivers the expected results. In this role, your responsibilities involve all aspects of quality control. You test procedures and make adjustments as required to meet goals and deadlines. As part of your duties, you log your findings and implement a plan for the smooth operation of the line for the long-term. Some people in this career specialize in a particular facet of the manufacturing process.

What are the key skills and qualifications needed to thrive as a Quality Associate, and why are they important?

To thrive as a Quality Associate, you need attention to detail, knowledge of quality control principles, and often a degree in science, engineering, or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and documentation software is typically required. Strong analytical thinking, communication skills, and problem-solving abilities help you collaborate across teams and address process issues effectively. These skills and qualities ensure that products and processes consistently meet standards, minimizing errors and maintaining compliance.

What are some common challenges Quality Associates face when working on cross-functional teams?

Quality Associates often collaborate with departments like manufacturing, engineering, and regulatory affairs to ensure product quality standards are met. One common challenge is balancing differing priorities—while production teams may be focused on output and speed, Quality Associates must prioritize compliance and thorough documentation. Navigating these competing interests requires strong communication skills and a proactive approach to problem-solving. Building positive relationships across teams and fostering a culture of quality can help overcome these challenges and ensure successful outcomes.

What are Quality Associates?

Quality Associates are professionals responsible for ensuring that products or services meet established quality standards before reaching customers. They assist in monitoring production processes, performing inspections, and documenting quality issues or defects. Quality Associates also help implement quality control procedures and work closely with other departments to resolve any quality-related problems. Their role is essential in maintaining compliance with regulatory requirements and ensuring customer satisfaction.

What does a QA associate do?

A QA associate is responsible for inspecting and testing products or processes to ensure they meet quality standards and specifications. They document issues, collaborate with production teams, and may use tools like checklists or testing software to identify defects and improve quality. Attention to detail and knowledge of quality procedures are essential for this role.

What is the difference between Quality Associate vs Quality Technician?

AspectQuality AssociateQuality Technician
Required CredentialsHigh school diploma or equivalent; some roles may prefer certifications like ASQ CQPAHigh school diploma; certifications like CQTA are common but not always required
Work EnvironmentOffice settings, manufacturing floors, labsManufacturing plants, labs, production lines
Employer & Industry UsageManufacturing, healthcare, aerospace, automotiveManufacturing, electronics, pharmaceuticals
Common Search & ComparisonOften compared for entry-level quality rolesSimilar roles but more technical focus

While both roles focus on quality assurance, a Quality Associate typically handles documentation, audits, and process improvements, often in office or administrative settings. A Quality Technician usually performs hands-on inspections, testing, and data collection directly on the production floor. Both roles are essential in maintaining product quality but differ in their daily tasks and work environments.

What are the most commonly searched types of Quality jobs in Quebec? The most popular types of Quality jobs in Quebec are:
What are popular job titles related to Quality Associate jobs in Quebec? For Quality Associate jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Quality Associate jobs in Quebec look for? The top searched job categories for Quality Associate jobs in Quebec are:
What cities in Quebec are hiring for Quality Associate jobs? Cities in Quebec with the most Quality Associate job openings:

Quality Operations Associate

Cameleon RH

Pointe-claire, QC • On-site

Full-time

Posted 3 days ago


Job description

\n <\/head>\n \n Quality Operations Associate<\/b><\/span>
<\/h1>Introduction
<\/h2>

At Cameleon, we believe that happiness at work comes from the right match between the right role, the right company, the right manager, and a stimulating environment where you can thrive.
<\/p>

Today, we are offering an exciting opportunity to join a well\-established company in the medical device industry, where quality, innovation, and patient safety are at the heart of everything they do.
<\/p>

If you are passionate about quality, detail\-oriented, and enjoy understanding, analyzing, and improving processes, this opportunity could be exactly what you are looking for!
<\/p>\n


Job Details
<\/h2>


<\/p>\n

\n Location:<\/b> Pointe\-Claire, QC
\n <\/div>\n
\n Employment Type:<\/b> Full\-time permanent position
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<\/p>\n


Work Environment
<\/h2>

You will join a well\-established organization in the medical device sector, recognized for the quality of its products and its strong commitment to patient safety.
<\/p>

You will work within a collaborative and multidisciplinary team, interacting with Commercial (Branded and Private Label), Operations, Customer Service, Supplier Quality, and Regulatory Affairs teams.
<\/p>

This is a dynamic environment where your ability to analyze, propose solutions, and drive improvements will have a real impact.
<\/p>\n


Your Day\-to\-Day Role
<\/h2>

As a Quality Operations Associate<\/b>, you will play a key role in managing quality activities, with a strong focus on complaint handling and continuous improvement.
<\/p>

More specifically, you will:
<\/p>\n

    \n
  • Manage customer complaints in an ISO 13485 regulated environment
    <\/li>\n
  • Lead and support quality investigations (root cause analysis, risk assessment, resolution)
    <\/li>\n
  • Ensure proper tracking and effectiveness of CAPAs (Corrective and Preventive Actions)
    <\/li>\n
  • Collaborate with cross\-functional teams to resolve quality issues
    <\/li>\n
  • Identify trends and recommend improvement actions
    <\/li>\n
  • Participate in internal audits and support compliance with the Quality Management System (QMS)
    <\/li>\n
  • Maintain accurate and compliant documentation in line with regulatory requirements
    <\/li>\n
  • Actively contribute to continuous improvement of quality processes
    <\/li>\n <\/ul>\n
    The Must\-Haves
    <\/h2>\n
      \n
    • College diploma (DEC) in a scientific field
      <\/li>\n
    • Minimum of 3 years of experience in an ISO 13485 regulated environment
      <\/li>\n
    • Experience in Quality Assurance (QA), ideally with complaint handling or CAPA
      <\/li>\n
    • Good understanding of Quality Management Systems (QMS)
      <\/li>\n
    • Strong communication skills in both French and English (written and spoken)
      <\/li>\n
    • Strong attention to detail, analytical mindset, and sound judgment
      <\/li>\n
    • Ability to manage multiple priorities in a fast\-paced environment
      <\/li>\n
    • Team player with a strong customer\-centric mindset
      <\/li>\n <\/ul>

      Nice to have:<\/b>
      <\/p>\n

        \n
      • Experience in complaint handling
        <\/li>\n
      • In\-depth knowledge of ISO 13485
        <\/li>\n
      • Experience with QMS and ERP systems
        <\/li>\n
      • Training or certification in Quality Assurance or Root Cause Analysis
        <\/li>\n <\/ul>\n
        6 Great Reasons to Apply!
        <\/h2>\n
          \n
        • Join a recognized company in the medical device industry
          <\/li>\n
        • Play a key role with direct impact on product quality and patient safety
          <\/li>\n
        • Work in a collaborative and stimulating environment
          <\/li>\n
        • Grow your expertise in a highly regulated quality environment
          <\/li>\n
        • Be involved in meaningful continuous improvement initiatives
          <\/li>\n
        • Enjoy a structured, supportive, and people\-focused workplace
          <\/li>\n <\/ul>\n
          Ready to Join the Adventure?
          <\/h2>

          We can't wait to meet you!
          <\/p>

          Send us your application today or reach out confidentially. At Cameleon, we are always looking for passionate talents ready to make a difference
          <\/p>\n

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