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Quality Control Associate Jobs in Montreal, QC (NOW HIRING)

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Quality Control Associate information

See Montreal, QC salary details

$10

$19

$33

How much do quality control associate jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for quality control associate in Montreal, QC is $19.81, according to ZipRecruiter salary data. Most workers in this role earn between $14.86 and $22.77 per hour, depending on experience, location, and employer.

What does a quality control associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

What are the key skills and qualifications needed to thrive as a quality control associate?

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges quality control associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

What is the difference between Quality Control Associate vs Quality Assurance Technician?

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

What are the most commonly searched types of Quality Control jobs in Montreal, QC?

The most popular types of Quality Control jobs in Montreal, QC are:

Infographic showing various Quality Control Associate job openings in Montreal, QC as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 11% Part Time, 5% Contract, and 2% Nights. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $41,195 per year, or $19.8 per hour.

Quality Operations Associate

Cameleon RH

Pointe-claire, QC • On-site

Full-time

Re-posted 27 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
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\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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