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Quality Auditor Jobs in Quebec (NOW HIRING)

As a Global GMP Quality Auditor at Novartis, you will play a critical role in ensuring compliance, quality, and patient safety across our global network. This is an opportunity to work with diverse ...

The Auditor, Medical Devices will support the Business Assurance business by leading and/or ... Review client's quality management system documentation * Verify and document evidence of ...

Collaborate closely with junior and senior auditors, as well as managers and partners, to ensure high-quality and efficient engagements. * Supervise intermediate auditors in the field and uphold firm ...

Document audit files and ensure quality control * Monitor the implementation of action plans ... Coordinate with external auditors: provide the required information and participate in the work as ...

... quality of the documentation * Act as a "coach" or resource person for your colleagues Your team ... Auditor profile : * Strong understanding of the audit process, including leading engagements ...

... ensuring the quality of the documentation * Act as a \"coach\" or resource person for your ... Auditor profile : * Strong understanding of the audit process, including leading engagements ...

... ensuring the quality of the documentation * Act as a \"coach\" or resource person for your ... Auditor profile : * Strong understanding of the audit process, including leading engagements ...

... ensuring the quality of the documentation * Act as a \"coach\" or resource person for your ... Auditor profile : * Strong understanding of the audit process, including leading engagements ...

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Showing results 1-20

Quality Auditor information

See Quebec salary details

$9

$19

$38

How much do quality auditor jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for quality auditor in Quebec is $19.93, according to ZipRecruiter salary data. Most workers in this role earn between $14.18 and $22.60 per hour, depending on experience, location, and employer.

What is a quality auditor?

Quality Auditors are professionals responsible for assessing and ensuring that products, services, or processes meet established standards of quality. They conduct audits, inspections, and reviews to identify areas of non-compliance and recommend improvements. Quality Auditors work in various industries, such as manufacturing, healthcare, and food production, to help organizations maintain regulatory compliance and deliver consistent quality. Their role is crucial in minimizing defects, ensuring customer satisfaction, and supporting continuous improvement initiatives.

What are the key skills and qualifications needed to thrive as a quality auditor, and why are they important?

To thrive as a Quality Auditor, you need a solid understanding of quality management systems, auditing techniques, and regulatory standards, often supported by a relevant degree or professional certification such as ISO 9001 Lead Auditor. Familiarity with audit management software, documentation tools, and industry-specific compliance systems is typically required. Attention to detail, analytical thinking, and strong interpersonal communication help Quality Auditors identify issues and work collaboratively on solutions. These skills are crucial for ensuring organizational compliance, continuous improvement, and the delivery of high-quality products or services.

What does a quality auditor do?

As a quality auditor, your main duties are to inspect a product or system to ensure that it meets the set specifications and standards, write audit reports and assessments, and develop quality control monitoring protocols. Your responsibilities depend on the specifics of your job. Some quality auditors are only responsible for checking a specific element of a product, such as consumer safety or standards compliance. For example, a sorter separates materials, such as fabrics, by color, size, or fabric type. A sample, on the other hand, may monitor a large batch product, such as paint, to ensure there are no defects in the run.

What are some common challenges quality auditors face when ensuring compliance across multiple departments?

Quality Auditors often encounter challenges such as varying levels of process understanding, resistance to change, and inconsistent documentation across departments. Successfully addressing these issues requires strong communication skills, adaptability, and the ability to build rapport with team members from different backgrounds. Auditors frequently collaborate with departmental leads to clarify standards, provide constructive feedback, and foster a culture of continuous improvement.

What is the difference between Quality Auditor vs Quality Inspector?

AspectQuality AuditorQuality Inspector
Primary RoleEvaluates quality management systems and processes to ensure compliance and continuous improvementInspects products or services to identify defects or deviations from standards
CertificationsISO Auditor, CQE, internal auditor certificationsNone specific, often trained in inspection techniques
Work EnvironmentOffice-based, audits conducted in various departments or facilitiesManufacturing floors, labs, or production lines
FocusProcess compliance and improvementProduct quality and defect detection

While both roles focus on quality, a Quality Auditor assesses systems and processes to prevent issues, whereas a Quality Inspector examines products directly to identify defects. Understanding these differences helps in choosing the right career path or hiring the appropriate professional for quality assurance needs.

How do I become a quality auditor?

To become a quality auditor, typically, candidates need a high school diploma or equivalent, with some roles requiring a bachelor's degree in a related field such as quality management, engineering, or business. Relevant certifications like Certified Quality Auditor (CQA) from the American Society for Quality (ASQ) can enhance job prospects, and experience in quality control or manufacturing environments is often preferred.

How much does a quality auditor get paid?

The average salary for a quality auditor typically ranges from $40,000 to $70,000 per year, depending on experience, industry, and location. Entry-level positions may start lower, while experienced auditors with certifications can earn higher wages, often with opportunities for overtime and bonuses.

What are popular job titles related to Quality Auditor jobs in QC?

For Quality Auditor jobs in QC, the most frequently searched job titles are:

Infographic showing various Quality Auditor job openings in Quebec as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, 3% Contract, and 1% Nights. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $41,458 per year, or $19.9 per hour.

Full-time

Posted 5 days ago


Job description

Band

Level 4


Job Description Summary

#LI-Remote
Location: Remote/Canada or Remote/Mexico. For the role posting in Mexico, please see REQ-10086366.
Novartis will not offer relocation support for this role.
Are you passionate about safeguarding quality and driving continuous improvement across a global healthcare organization? As a Global GMP Quality Auditor at Novartis, you will play a critical role in ensuring compliance, quality, and patient safety across our global network. This is an opportunity to work with diverse manufacturing sites, development centers, contract manufacturers, laboratories, warehouses and suppliers, using your expertise to identify risks, strengthen quality systems, and influence positive change. If you thrive in a collaborative environment and are motivated by making a meaningful impact on healthcare around the world, we encourage you to apply.


Job Description

Key Responsibilities

Plan, lead, and execute GMP audits across global operations and external partners.

Assess compliance with regulations, quality standards, procedures, and guidance documents.

Document audit observations, prepare reports, and communicate findings to stakeholders.

Review and approve corrective and preventive action plans addressing audit findings.

Provide expert guidance and training on audit activities.

Escalate critical compliance issues and support timely mitigation activities when required.

Maintain expertise in evolving regulations, industry standards, and quality expectations.

Essential Requirements

Degree in Chemistry, Pharmacy, Biology, Engineering, or another related scientific discipline; other degrees with relevant experience may be considered.

Minimum 10 years of broad experience in the pharmaceutical or medical device industry, including QA/QC management and manufacturing, development, or other relevant experience such as working at a regulatory health authority.

Expertise in at least one of the following areas: drug product (DP) manufacturing, biologics, sterile manufacturing, laboratories, microbiology, packaging, active pharmaceutical ingredients (API), excipients, medical devices, computer system validation, or quality systems.

Excellent knowledge of regulatory requirements, with experience and/or interaction with local Health Authorities and sporadically with other Health Authorities; sound and practical judgement in the interpretation and application of regulations and standards.

Strong interpersonal skills, including diplomacy, persuasion, and stakeholder management.

Willingness to travel approximately 60% globally.

Excellent oral and written English communication skills.

English language proficiency is required due to the need to participate in national and international meetings conducted in English and review scientific and strategic materials primarily available in English. These responsibilities are an essential part of the role and cannot be performed solely in French.

DesirableRequirements

3 years auditing experience

Proficiency in an additional language such as German, French, Italian, Chinese, or Spanish.

At Novartis Canada, we are determined to be a valued partner and advocate, with a deep understanding of patient needs along the entire care journey - from drug development, to diagnosis, to access and beyond. Part of the way we are doing this is by leveraging data, technology, and partnerships.

Research & Development: we focus on four core therapeutic areas: Cardiovascular, Renal & Metabolic, Immunology, Neuroscience and Oncology. We also develop and deliver treatments through other promoted and established brands, which today are helping millions of patients. Over the last three years, our average annual research and development investment in Canada was over $30 million, and we conduct clinical trial research in every region throughout Canada.

Commitment to Diversity and Inclusion: Novartis is committed to building outstanding, inclusive work environment and diverse team's representatives of the patients and communities we serve.


Skills Desired

Collaboration, Data Integrity, Decision Making, Leadership, Risk Management