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Qc Associate Jobs in Ontario (NOW HIRING)

Based in Etobicoke, Auto Kool services its customers through a network of six (6) distribution centers across Canada located in Toronto [ON], Ottawa [ON], Montreal [QC], Moncton [NB], Dartmouth [NS ...

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Shipping Associate

Etobicoke, ON · On-site

CA$18 - CA$22/hr

The Shipping Associate is responsible for managing the accurate and timely movement of goods from ... Perform quality control checks on outgoing shipments * Load and unload goods safely using ...

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... Associate (CQIA) certification is an asset. Work Experience: · Minimum 2-5 years of experience in quality assurance, quality control, process engineering, or within a manufacturing/industrial ...

Warehouse Associate Additive manufacturing and metrology are changing the way we design and ... Attention to detail and a keen eye for quality control * Ability to multitask * Experience with ...

... QC. We have 15 technical sales reps providing Canada-wide consultation & solution-sales of ... What do our Warehouse Associates do? The primary purpose of this role is to be responsible for ...

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... Associate is an asset. Work Experience: * Minimum one (1) year relevant work experience in quality assurance, quality control, process engineering and industrial settings or experience working in a ...

Showing results 21-40

Qc Associate information

See Ontario salary details

$10

$19

$33

How much do qc associate jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for qc associate in Ontario is $19.86, according to ZipRecruiter salary data. Most workers in this role earn between $14.90 and $22.84 per hour, depending on experience, location, and employer.

What is a QC associate?

A QC (Quality Control) Associate is a professional responsible for performing tests and inspections on products, materials, or processes to ensure they meet established quality standards. They work primarily in manufacturing, pharmaceutical, biotechnology, or food industries, helping to identify defects and maintain compliance with regulatory requirements. QC Associates document their findings, report issues, and may assist in implementing corrective actions to improve product quality. Their work is critical in ensuring that only safe and effective products reach customers.

What skills and qualifications are needed to be a QC associate?

To thrive as a QC Associate, you need a background in chemistry, biology, or a related scientific field, often supported by a relevant degree or laboratory experience. Familiarity with laboratory equipment, analytical instruments (like HPLC or GC), and quality management systems (such as GMP or ISO standards) is typically required. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for ensuring accuracy and collaborating with team members. These competencies are essential for maintaining product quality, regulatory compliance, and operational efficiency in quality control environments.

What challenges do QC associates face when ensuring product quality, and how can they be addressed?

QC Associates often encounter challenges such as tight production deadlines, handling multiple testing protocols, and maintaining accuracy under pressure. Adapting to new technologies or updated regulatory standards can also present difficulties. To address these, strong organizational skills, continuous training, and effective communication with cross-functional teams are essential. Additionally, maintaining thorough documentation and proactively identifying potential issues can help ensure consistent product quality and compliance.

What are the most commonly searched types of Qc jobs in Ontario?

The most popular types of Qc jobs in Ontario are:

What are popular job titles related to Qc Associate jobs in Ontario?

For Qc Associate jobs in Ontario, the most frequently searched job titles are:

What job categories do people searching Qc Associate jobs in Ontario look for?

The top searched job categories for Qc Associate jobs in Ontario are:

What cities in Ontario are hiring for Qc Associate jobs?

Cities in Ontario with the most Qc Associate job openings:

Infographic showing various Qc Associate job openings in Ontario as of August 2026, with employment types broken down into 1% As Needed, 64% Full Time, 33% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $41,311 per year, or $19.9 per hour.

Associate Quality Lead (Quality Assurance Programs)

Roche

Mississauga, ON • On-site

Full-time

Posted 16 days ago


Roche rating

9.3

Company rating: 9.3 out of 10

Based on 23 frontline employees who took The Breakroom Quiz

3rd of 86 rated pharmaceutical


Job description

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

Are you ready to shape the future of quality management in healthcare? As an Associate Quality Lead within our Pharma Development Quality (PDQ) function, you will play a vital role in supporting the delivery of quality-focused strategies that reinforce trust in our Quality Management System (QMS). Working with a high degree of independence, you will collaborate with cross-functional teams to ensure our clinical and safety data meets rigorous global regulatory standards.

In this dynamic position, you will have the unique opportunity to champion a culture of continuous improvement and innovation. By leveraging data analytics and digital tools, you will help optimize data collection and provide key insights that directly support our mission of delivering life-changing medicines to patients faster and more securely.

The Opportunity:

  • Implement Quality Strategies: Support the design, execution, and tracking of risk-based quality management strategies across the PDQ portfolio.

  • Deliver Quality Assurance: Execute targeted activities to assess quality assurance status and generate confidence in our end-to-end systems.

  • Manage Quality Data: Enhance data collection procedures, perform ad-hoc analyses, and deliver high-quality data insights to fulfil external regulatory needs.

  • Present to Health Authorities: Demonstrate the effective implementation of quality strategies.

  • Drive Compliance Projects: Participate in departmental or cross-functional compliance initiatives aimed at optimizing daily operations.

  • Champion Innovation: Drive the adoption of innovative digital tools and technologies into daily workflows to foster a proactive quality culture.

  • Foster Collaboration: Build and maintain an inclusive, supportive work environment while executing departmental goals and initiatives under limited supervision.

  • Audit Execution: Utilize AI and automated tools to execute audits and synthesize audit evidence.

  • Inspection Support: Provide logistical and compliance support for GCP inspections, including scribe duties and back-room document QC.

Who You Are

You are a proactive, organized professional looking to elevate your career in quality management within a global, life-changing industry. You thrive in environments that value continuous learning, offer room for professional growth, and empower you to work independently to make a genuine impact on patient outcomes.

To be successful in this role, you bring:

  • A Bachelor's degree in a scientific or quality-related discipline, or an equivalent combination of education and 1-3 years' of experience.

  • Experience within the pharmaceutical, biotech, or medical device industry, with a foundational understanding of product development and GxP regulations (e.g., GCP, GVP, MDR).

  • Strong digital and data literacy, with the ability to interpret data and translate it into actionable quality insights.

  • Exceptional organizational and execution skills, alongside a demonstrated ability to take ownership of projects proactively.

  • Developing expertise in Critical to Quality (CtQ) factors and functional group operations.

  • Fluency in written and spoken English, with strong presentation skills.

Relocation Benefits are not available for this job posting.

#MQRS

The expected salary range for this position based on the primary location of Mississauga is 89,256.00 and 117,148.50 of hiring range. Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.

We use artificial intelligence to screen, assess or select applicants for this role.

This posting is for an existing vacancy at Hoffmann-La Roche Ltd.

Who we are

A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.


Let's build a healthier future, together.

Roche is an Equal Opportunity Employer.


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