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

Ensure control of defective WIP materials (quarantine, retention, and disposal areas) to keep ... quality roles. * Prior experience working in a GMP setting. * Knowledge of cGMP, ISO, and ...

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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 ...

... quality control checks on products before they are shipped ou · Supporting assembly, extra support, and other warehouse related request when needed · Adhere to all company policies and procedures ...

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 ...

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 ...

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

See Vaughan, ON salary details

$9

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$32

How much do quality control associate jobs pay per hour?

As of Jul 18, 2026, the average hourly pay for quality control associate in Vaughan, ON is $18.79, according to ZipRecruiter salary data. Most workers in this role earn between $14.10 and $21.61 per hour, depending on experience, location, and employer.

What is a QC Associate job description?

A Quality Control (QC) Associate is responsible for inspecting and testing products or materials to ensure they meet quality standards and specifications. They document findings, identify defects, and collaborate with production teams to address issues, often using tools like measurement instruments and quality management systems. The role typically requires attention to detail, knowledge of quality procedures, and adherence to safety protocols.

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, and why are they important?

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.

Which pays more, QA or QC?

Quality Assurance (QA) and Quality Control (QC) roles often have similar pay scales, but QA positions typically offer higher salaries due to their focus on process improvement and prevention. Factors such as industry, experience, certifications, and location can influence compensation for both roles.

What do quality control associates do?

Quality control associates inspect products, materials, or processes to ensure they meet quality standards and specifications. They perform tests, document findings, and may use tools like calipers or microscopes, often working in manufacturing or production environments to identify defects and ensure product consistency.

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.

Is QC a high paying job?

The salary for a Quality Control Associate varies depending on industry, experience, and location, but it is generally considered an entry-level to mid-level position with moderate pay. Higher salaries are often associated with advanced certifications, specialized skills, or supervisory roles within quality control departments.
What cities near Vaughan, ON are hiring for Quality Control Associate jobs? Cities near Vaughan, ON with the most Quality Control Associate job openings:
Infographic showing various Quality Control Associate job openings in Vaughan, ON as of July 2026, with employment types broken down into 94% Full Time, and 6% Part Time. Highlights an 94% In-person, and 6% Hybrid job distribution, with an average salary of $39,086 per year, or $18.8 per hour.
Quality Associate-II, QA Assurance

Quality Associate-II, QA Assurance

Baxter

Alliston, ON • On-site

CA$86K - CA$129K/yr

Full-time

Posted 8 days ago


Job description

This is whereyour work makes a difference.

At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job-you will find purpose and pride.

Your Team at Baxter

Within Quality, every role matters. Baxter's products are shipped worldwide to patients in need. Whether you build new processes or solve unique production challenges, you have the trust and chance to bring creativity. No matter your role, your work will impact part of our global operation.

The mission of Baxter is to save and sustain lives. This mission is embedded into everything we do. This means if there is a decision to be made where quantity and quality are at odds, we will always choose quality. Our patients come first, always.

The Quality function values both working together as a team and independently. We draw energy from working in a plant or an office where there are opportunities to collaborate. As the company evolves, so does the way our team approaches work as it strives to build top-of-the-line products.

We build relationships with each other to get work done. Building these relationships is easy because we all share common traits of being reliable, ethical, and caring. We lean on our colleagues for their expertise and hold each other accountable. We feel empowered to speak up when there's a new insight or opportunity to improve something. This open dialog builds trust within the team and helps develop a better product for our customers.

What you'll be doing
  • Provide front line day-to-day assistance on product quality issues to ensure GMP, regulatory and procedural compliance to maintain high standards of quality.
  • Support during assigned Shift, with the requirement to support plant overtime and planned shutdowns when applicable.
  • Provide technical assistance on review and approval of department-related procedural changes, product quality concerns, reinspections, new product introductions, and protocols.
  • Support timely follow-up on quality exceptions and their preventative/corrective actions.
  • Support initiation/investigation and approvals of non-conformance events in the Trackwise system.
  • Act as SME for Electronic Batch Record (EBR) and SPC or equivalent experience.
  • Perform change control assessments/executions and approvals.
  • Ensure control of defective WIP materials (quarantine, retention, and disposal areas) to keep segregation, movement, documentation, and timely follow-up within the plant in sync with regulatory and compliance requirements.
What you'll bring

Required:

  • University Degree or equivalent experience, Bachelor of Science or equivalent experience.
  • 1 - 3 years' experience in manufacturing and quality roles.
  • Prior experience working in a GMP setting.
  • Knowledge of cGMP, ISO, and regulatory standards.
  • Diligent with the ability to work effectively under pressure.
  • Strong written and verbal communication abilities, negotiation capabilities, and the capacity to collaborate with individuals at every level of the organization.
  • Ability to build positive relationships and partner with internal and external collaborators.
  • Strong ability to balance multiple priorities.
  • Strong analytical and problem-solving skills with critical thinking abilities.
  • Intermediate to Advanced proficiency in MS Office Suite.
Preferred:
  • 3+ years with exposure to various areas of the manufacturing environment.
  • Experience in pharmaceutical, healthcare, or food manufacturing environments.
  • Experience with continuous improvement methodologies, Lean 6S, Kaizen, TPM, DMAIC.

Join us in our mission to make a global impact with your outstanding skills and dedication to quality!

Garbing Processes

We understand that compensation is an important factor as you consider the next step in your career. At Baxter,we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated salary range for this position is $86,400 - $129,600 annually, which reflects base salary as wellas estimated target payout under the Management Incentive Compensation Plan. Individual pay will bedetermined based upon skills, expertise and experience, and the incentive, which is contingent upon company andindividual performance outcomes. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

This posting is for a current existing vacancy within our organization. We are actively seeking qualified candidatesto fill this open position. If you are interviewed for this position, we will advise you within 45 days of the interview
as to whether or not you were successful in obtaining the position. Information submitted as part of the jobapplication process will be kept on file for 3 years from the date of submission in accordance with legislative
requirements.

As part of our recruitment process, Baxter Corporation may use AI tools to assist screening candidates and assistin evaluating candidate qualifications. All final hiring decisions are made by the hiring manager and recruitmentteam

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice
Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.