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Quality Control Associate Jobs in Ajax, ON (NOW HIRING)

JMR Personnel Services Ltd

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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 ...

Proto3000

Warehouse Associate

Maple, ON · On-site

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 ...

MD Analytics

Research Associate

Toronto, ON

Research Associate based in the Greater Toronto Area Working with a team in Toronto, you will be ... Key areas of focus include quality control for scripting, managing fieldwork, note-taking, creating ...

Harry Rosen, Inc.

Logistics Associate

Toronto, ON

CA$18.50 - CA$19.19/hr

Logistics Associate Full-Time, Permanent Harry Rosen, Bloor St. Your Style, Your Career Harry Rosen ... Follow quality control and receiving processes for all incoming goods * Prep product for placement ...

Fuller Landau LLP

Senior Associate, Audit

Toronto, ON · Hybrid

CA$80K - CA$95K/yr

Senior Associate, Audit Location:Toronto office, Hybrid Job vacancy status: Existing vacancy ... Plan, execute, and complete assurance engagements through to completion including all reviews, Q/C ...

Tremco CPG Inc.

Outside Sales Associate

Woodbridge, ON

CA$60K - CA$80K/yr

Montreal, QC If you are an ambitious, self-motivated individual with a proven record of effort ... Associate's degree (AAS), or Trade School Certification, or Bachelor's Degree (BS) preferred.

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Quality Control Associate information

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How much do quality control associate jobs pay per hour?

As of Aug 3, 2026, the average hourly pay for quality control associate in Ajax, ON is $17.97, according to ZipRecruiter salary data. Most workers in this role earn between $13.48 and $20.66 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 Ajax, ON? The most popular types of Quality Control jobs in Ajax, ON are:
What cities near Ajax, ON are hiring for Quality Control Associate jobs? Cities near Ajax, ON with the most Quality Control Associate job openings:
Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Ajax, ON as of July 2026, with employment types broken down into 94% Full Time, and 6% Nights. Highlights an 82% In-person, and 18% Hybrid job distribution, with an average salary of $37,369 per year, or $18 per hour.

Quality Assurance Associate

Apollo Health And Beauty Care

Toronto, ON • On-site

CA$52K - CA$60K/yr

Full-time

Medical, Dental

Posted 23 days ago

Job description

Benefits:
  • Gym Access
  • Dental insurance
  • Health insurance

We're Hiring!
The Quality Assurance Associate participates in the completion of milestones associated with specific projects and supports ongoing Annual Product Reviews, Management of Deviations, CAPAs, Change Management, SOP Management, and general quality management systems responsibilities in support of the manufacture, packaging and release of commercial products.
JOB RESPONSIBILITIES

  • Completes APR reports in accordance with the schedule, gathering information available from batch records, investigations, product changes, complaints etc.
  • Collaborate and liaise with business to review and manage Change Control Requests. Ensures GDP and change management procedures are followed.
  • Assists with monitoring all internal QMS compliance through performing internal audits, including production, facilities, validation, and the laboratories.
  • In collaboration with Quality colleagues identifies areas for continuous improvement within the QMS.
  • Acts as Subject Matter Expert (SME) for Investigations & Quality Risk Management. 
  • Reviews deviation and investigation records, includes tracking, follow-up, and reporting/trending. Ensures GDP and deviation procedures are followed.
  • Reviews Corrective and Preventative Actions (CAPA); includes tracking, follow-up, and reporting/trending and evaluating CAPA for effectiveness.
  • Works with all departments to guide the timely completion of Deviations, CAPA, Corrective Work Orders, Change Controls, and Investigations.
  • Helps the Compliance Specialist with the review of batch records for product release.
  • Generates and maintains Quality Assurance and QMS standard operating procedures (SOPs).
  • Oversees controlled document and system changes and performs detailed impact analysis to ensure all necessary GMP and qualification action items have been added to the change controls, as well as executed.
  • Collaborates significantly with cross functional groups, including Quality Assurance, Manufacturing, Process Development, Facilities, and Regulatory Affairs on quality assurance matters. 
  • Cross-train with other QA Associates.
  • Responsible for Logbook issuance, control, and review.
  • Files and maintains controlled documents.
  • Other duties as assigned
JOB REQUIREMENT

  • Minimum 5 years of GMP-related experience in biopharmaceutical or pharmaceutical manufacturing.
  • Bachelor's degree or diploma in Chemistry, Biology, Engineering, or a related field.
  • Strong knowledge of cGMP/GDP requirements, international regulatory compliance, and GMP operations.
  • Proven ability to prioritize tasks and meet internal and external customer needs in a fast-paced environment.
  • Experience supporting Quality projects, including data analysis and evaluation of identifiable factors.
Apollo Health & Beauty Care Ltd. will ensure accommodations are available in consultation with candidates during all stages of the recruitment process. The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job. Duties outlined in this job description may not be all-inclusive, and can be modified at any time if requested by management. Apollo is committed to providing accommodations for people with disabilities in all parts of the hiring process. Apollo will work with applicants to meet accommodation needs that are made known in advance.
We thank all applicants for their interest however only those meeting the minimum qualifications will be interviewed.
Vacancy Status: This posting represents an existing vacancy, and we are actively recruiting to fill this position.