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Qa Associate Jobs in Hamilton, ON (NOW HIRING)

Quality Assurance Engineer Location: Remote Reporting to: Engineering Squad Lead About the Role We are looking for a Quality Assurance Engineer to join our team at 1VALET. This role is critical to ...

As a QA analyst plays critical role in making sure the quality of product/ project is as per the requirement before it is pushed to production QA analyst participates in all phases of projects ...

Quality Assurance Specialist

Ottawa, ON ยท Hybrid

CA$88K - CA$110K/yr

Job Posting Title Quality Assurance Specialist Job Category Operations Training Delivery Language Requirements Bilingual Required / Bilingue requis English and French are required / Le francais et ...

Position Summary The Quality Assurance Representative (QAR) will be the representative for quality matters related to specific customers or products and will coordinate the activities to ensure ...

QA Analyst

Ottawa, ON ยท On-site +1

LeverageTek is actively seeking a QA Analyst (MS Dynamics CRM) for a 6 month contract with its Ottawa based customer. Work Location: Hybrid Ottawa - Open to remote Key Tasks Create and execute test ...

QA Analyst

Ottawa, ON ยท On-site +1

LeverageTek is actively seeking a QA Analyst (MS Dynamics CRM) for a 9 month contract with its Ottawa based customer. Work Location: Hybrid Ottawa - Open to remote Key Tasks Create and execute test ...

Quality Assurance Specialist

Kitchener, ON ยท On-site

CA$25 - CA$30/hr

Reports audit findings to Director QA or designate and conducts post-audit meetings as necessary. * Performs/ reviews non-conformance investigations to ensure the non-conformance has been addressed ...

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Qa Associate information

See Hamilton, ON salary details

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How much do qa associate jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for qa associate in Hamilton, ON is $23.68, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $28.98 per hour, depending on experience, location, and employer.

What is a QA associate?

QA Associates, or Quality Assurance Associates, are professionals responsible for monitoring, inspecting, and proposing measures to improve processes that ensure the quality of products or services in a company. They work closely with production, development, and compliance teams to make sure that products meet required standards and regulations. Their tasks often include reviewing documentation, conducting audits, and reporting on quality metrics. QA Associates play a crucial role in maintaining customer satisfaction and regulatory compliance in industries such as pharmaceuticals, manufacturing, and software.

Is a QA associate a difficult job?

A QA associate role involves testing products or software to identify defects, which requires attention to detail, analytical skills, and knowledge of testing tools. The job can be challenging depending on project complexity and deadlines but is generally manageable with proper training and experience.

What are some common challenges faced by a QA associate, and how can they be addressed?

QA Associates often encounter challenges such as managing tight deadlines, adapting to rapidly changing project requirements, and ensuring thorough test coverage. Effective communication with developers and other team members is crucial to address issues quickly and maintain product quality. Staying organized, using test management tools, and participating in regular stand-up meetings can help QA Associates stay on top of their workload and deliver consistent results.

What does a QA associate do?

A QA associate is responsible for testing products, software, or processes to ensure they meet quality standards and specifications. They develop test plans, identify defects, document issues, and work with teams to improve quality, often using testing tools and following industry protocols.

Is QA a good entry level job?

A QA Associate role is often suitable for entry-level candidates, as it typically requires basic knowledge of testing processes, attention to detail, and familiarity with testing tools. It provides a good foundation in quality assurance practices and can lead to more advanced positions in software development or testing. However, some roles may prefer candidates with prior experience or certifications in quality assurance or related fields.

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

To thrive as a QA Associate, you need a solid understanding of quality assurance methodologies, attention to detail, and often a degree in a scientific or technical field. Familiarity with tools like LIMS, GMP/GLP regulations, and quality management systems, as well as relevant certifications such as ASQ or Six Sigma, is typically required. Strong analytical thinking, effective communication, and problem-solving abilities help you excel within cross-functional teams. These skills ensure product compliance, support continuous improvement, and maintain high standards in regulated environments.
What are the most commonly searched types of Qa jobs in Hamilton, ON? The most popular types of Qa jobs in Hamilton, ON are:
What cities near Hamilton, ON are hiring for Qa Associate jobs? Cities near Hamilton, ON with the most Qa Associate job openings:
Infographic showing various Qa Associate job openings in Hamilton, ON as of July 2026, with employment types broken down into 1% As Needed, 65% Full Time, 32% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $49,264 per year, or $23.7 per hour.

Quality Assurance Assoc Specialist

Zimmer Biomet Canada, Inc

Mississauga, ON โ€ข Hybrid

CA$55K - CA$65K/yr

Other

PTO

Posted 14 days ago


Job description

Valued Team member: We are glad you are exploring new opportunities within Zimmer Biomet!


What You Can Expect

Responsible for gathering relevant and factual information plus data in order to solve quality related problems. Resolve issues by identifying and applying solutions from acquired technical experience and guided precedents. Plan and execute projects by identifying and organizing activities into time dependent sequencing with realistic timelines. Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Quality goals.

This is a hybrid position, 3 days onsite per week.

How You'll Create Impact
  • Support improvement of Quality Management Systems (QMS) aligned with international standards and corporate policies.
  • Perform Quality Systems maintenance activities including drafting and reviewing SOPs, implementing training programs, providing cross-functional training, and participation in internal audits.
  • Assist with Health Canada inspections and corporate / third party audits.
  • Monitor and communicate changes in global/local regulatory requirements and international standards; ensure compliance and continuity of business operations.
  • Execute product hold workflow from initiation phase through resolution.
  • Develop and implement corrective / preventative action plans.
  • Perform product and process containment to reduce risks and impact of the nonconformance, utilize root cause analysis tools (e.g. 5 Why, Ishiwaka) and assist with all aspects of investigation, documentation and data collection.
  • Support KPI data collection and trending, coordination of management reviews and quality systems reviews.
  • Assist with supplier management processes, including new supplier onboarding and approval, supplier monitoring and supplier corrective action plans
  • Assist with product complaints, recalls, incident reports, FRNs as necessary.
What Makes You Stand Out
  • Knowledge of the Canadian Food and Drugs Act, Canada Medical Device Regulations & Canada CTO regulations.
  • Knowledge of ISO 13485:2016 standard.
  • Excellent team collaboration and teamwork skills.
  • Strong attention to detail; project/submission management skills, ability to multi-task and balance competing priorities.
  • Knowledge of overall business environment, the orthopaedic industry, and the marketplace.
  • Ability to learn and stay abreast of regulations pertinent to medical devices, biologics, in-vitro diagnostic devices and combination products as needed, based on functional area.
  • Ability to build relationships between Quality Assurance and other areas of the organization; ability to communicate effectively at all levels.
  • Strong writing, communication, and interpersonal skills.
  • Ability to identify risk in business strategies.
  • Strong problem-solving skills.
  • Effective negotiating skills.
Your Background
  • Bachelor's degree required, science or engineering discipline preferred.
  • 0-2 years of relevant experience required.
  • Post grad studies or certification in RAQA required.
  • Advanced science degree preferred.
  • Experience in Regulatory Affairs, Engineering, Quality, or related field considered an asset.
  • Certification as a quality engineer (e.g. CQE) or Supplier Quality Profession (CSQP) granted through the American Society of Quality (ASQ), or Certified in Project Management (e.g. CAPM, APM) preferred.
  • A combination of education and experience may be considered.
Travel Expectations

Up to 5%

Expected Compensation Range

$55,000 - $65,000 CAD/annual

Holiday and PTO provided

This is a new position


EOE/M/F/Vet/Disability

Employment Type: OTHER