309 Quality Management jobs in Canada

Job Description

We are currently seeking a Manager, Quality Management System (QMS) to take ownership of our compliance, audit, and continuous improvement processes. This is a critical leadership role, responsible for ensuring our QMS remains robust, efficient, and fully aligned with AS9100, ISO 9001, and customer-specific requirements.

Your Mission:

In this role, you won’t just manage quality systems, you’ll lead a culture of compliance and accountability across all programs, departments, and shop-floor activities. From planning internal audits to interfacing with third-party certifiers, you be the driving force behind our commitment to excellence.

What You’ll Be Responsible For:

 Leading, planning, and executing internal QMS audits aligned with AS9100
Managing receiving inspection activities and part conformity
riving Root Cause Corrective Actions (RCCA) from customer feedback
oordinating and hosting internal, supplier, and third-party audits
wning and overseeing the DSQR process
cting as the key liaison with external auditors during site audits and certifications
dministering the QMS in line with our Quality Manual and applicable standards
uiding and mentoring cross-functional teams in quality system practices and audit protocols
eading Management Review Meetings and reporting on QMS performance
elivering clear recommendations for continuous improvement

What You Bring to the Table:

degree or diploma in Mechanical, Manufacturing, or Process Engineering
ertification as an ISO 9001/AS9100 auditor
0+ years in quality assurance within a manufacturing environment, including management-level responsibilities
eep knowledge of AS9100, ISO standards, and aerospace or nuclear sector requirements
roven leadership in problem-solving, process improvement, and compliance
trong communication skills with the ability to lead audits, write reports, and collaborate with customers
confident, data-driven decision-maker with hands-on experience in quality tools and methodologies

Salary: $80-90k 

*** Only qualified who meet all of the requirements will be considered. Thank you and good luck with your search! 

Job Description

Our customer, a major oil and gas producer, is looking for a Quality Assurance Quality Management Plan Coordinator.  This is a long-term position based in downtown Calgary, but there will be monthly traveling within Alberta. The work schedule is 5 days a week, but the summer schedule is 4 days a week. The successful candidate will be responsible for reinforcing the safety codes act, specifically the B149 Gas Code within knowledge on Industrial building design and gas fitting.  This is a diverse role so the successful candidate will have a growth mindset.

Key Accountabilities :

• Ensure the Quality Management Plan (QMP) is adhered to in an effective manner by taking a proactive approach working with a variety of stakeholders.
• Provide technical expertise in the Alberta Safety Codes system, including the Act, regulations, Alberta Building Code, B149 gas codes and National Plumbing Code.
• Perform preliminary code analysis, provide technical support, recommendations, and code interpretation to project teams.
• Plan inspections by third party safety code officers.
• Review and coordinate documentation exchanged between projects and safety code officers.
• Effectively manage large amounts of data and documentation.
• Identify opportunities to use data for decision making and identifying areas of continuous improvement.

• Civil, Mechanical, Instrumentation Engineer/EIT/CET, Architect, Gasfitter, Plumber, Safety Code Officer.
• Highly motivated individual with excellent organization and communication abilities, problem solving skills, and attention to detail.
• Previous work experience in oil and gas industry, construction projects, or with regulatory / government agencies.
• Exposure to safety codes compliance programs, and experience using National Building Code – Alberta Edition or CSA B149 Gas Codes is considered an asset.

Job Description

Company Description

One of Canada's Best Diversity Employers and Greater Toronto's Top Employers for many consecutive years, William Osler Health System (Osler) provides a safe and supportive health care network to grow your career. Osler is nationally recognized for its commitment to patient safety and is Accredited with Exemplary Standing, the highest rating a Canadian hospital can receive. As a major Ontario hospital system, and home to some of the biggest specialty and emergency departments in the country, Osler serves the 1.3 million residents of Brampton, Etobicoke and surrounding communities. We are proud to offer you incredible exposure to best-in-class health care delivery and challenging hands-on opportunities to stay at the top of your game.

A hospital system built for and by the community, we continue to expand our services to meet the needs of a growing population, creating opportunities for increased hands-on skills development, cross-department training and promotional opportunities. Guided by our accomplished senior leadership team, together we are driving our vision of patient-inspired health care without boundaries.

At Osler, we invest in careers that go beyond where health care professionals like you can achieve their goals and find deep personal and professional fulfillment. Join our team today!

Reporting to the Director, Quality and Practice, the Quality Improvement and Patient Safety Consultant has a keen interest and demonstrated experience in leading and facilitating processes related to quality improvement, patient safety, accreditation, and critical incident management. This role is responsible for supporting corporate initiatives and working with organizational leadership and staff to develop policies and procedures that ensure high-quality care, minimize patient harm, and foster a culture of continuous improvement.

A key focus of this role includes the implementation and sustainability of accreditation standards, ensuring compliance with national best practices and regulatory requirements. The consultant will play an integral role in supporting the organization’s Quality Improvement Plan (QIP) by facilitating the selection, monitoring, and achievement of quality indicators aligned with strategic priorities. Additionally, the role involves analyzing patient safety incident data and patient care trends to drive evidence-based improvements and proactively address potential risks.

The Quality Improvement and Patient Safety Consultant collaborates with key stakeholders to implement solutions for identified improvement opportunities, map out new processes, test changes, and evaluate the impact of quality and patient safety initiatives. This includes supporting accreditation readiness activities, such as facilitating mock surveys, preparing evidence submissions, coordinating tracer activities, and ensuring alignment with Accreditation Canada standards.

In addition, this position supports the critical incident management process, assisting clinical leaders with the identification, review, and resolution of incidents. The consultant will coordinate and facilitate root cause analyses, lead interdisciplinary debriefings, and help translate learnings from incidents into system-level improvements. They will also play a key role in embedding a Just Culture approach, ensuring that lessons learned contribute to proactive risk mitigation strategies.

The Quality Improvement and Patient Safety Consultant plays a critical role in advancing the organization’s quality, accreditation, and patient safety agenda. This position is responsible for implementing evidence-based quality improvement strategies, leading accreditation activities, and supporting the successful execution of the Quality Improvement Plan (QIP) to enhance patient care outcomes. The consultant works closely with clinical leaders, frontline staff, and interdisciplinary teams to drive improvements that align with the organization’s strategic priorities and accreditation standards.

Accountabilities:

• Conduct surveillance and analysis of patient safety incidents, quality indicators, and accreditation-related metrics to identify trends and areas for improvement.
• Lead and support the coordination of critical incident reviews, root cause analyses, and accreditation tracers, ensuring key learnings drive system improvements.
• Collaborate with clinical leaders and staff to develop and implement policies, procedures, and improvement strategies that enhance quality, safety, and accreditation readiness.
• Support the planning, implementation, and monitoring of the Quality Improvement Plan (QIP) to ensure measurable improvements in patient care outcomes.
• Engage frontline staff in quality and patient safety initiatives, including education, knowledge translation, and participation in accreditation activities.
• Provide project management and data analysis support for quality improvement, accreditation, and risk management initiatives.
• Maintain and optimize systems that support patient safety incident reporting, accreditation evidence collection, and QIP progress tracking.
• Attend and contribute to various quality, patient safety, and accreditation committees as required.

• Undergraduate Degree in related field (business administration, health care administration, health profession)
• College degree/certificate in clinical practice or risk management, health care administration
• Three years work experience in clinical risk management, quality improvement, accreditation or related field in health care
• Critical incident management or patient safety and accreditation experience within the last three years preferred
• Member of a Regulated College in Ontario preferred
• Certified Risk Management designation an asset
• Demonstrated understanding of acute care environment
• Demonstrated understanding of quality improvement, patient safety methodologies
• Self-directed and able to deal with multiple stakeholders while managing multiple priorities and workload management
• Ability to work in a team based environment
• Exceptional computer skills
• Data management and statistical experience desirable
• Proven ability to remain up-to-date with health care quality assurance trends, practices and legislation
• Experience in collecting, analyzing, interpreting data and reporting for the purposes of quality improvement or critical incident management
• Experience in managing broad (e.g. hospital-wide) improvement projects
• Must demonstrate Osler's Values of Respect, Excellence, Service, Compassion, Innovation and Collaboration

Hours: Currently days, Monday to Friday (subject to change in accordance with operational requirements)

INTERNAL APPLICATION DEADLINE : August 27, 2025

POSTED :  August 13, 2025

Annual Salary:

Minimum: $88,413.00/yearly
Maximum: $110,526.00/yearly

#FT

#LI-RS1

Osler values inclusivity and diversity in the workplace. We welcome and encourage applicants from diverse backgrounds. We are committed to providing accessible employment practices that are in compliance with the Accessibility for Ontarians with Disabilities Act. If you require an accommodation at any stage of the recruitment process, please notify Human Resources at

While we thank all applicants, only those selected for an interview will be contacted. Any information obtained during the course of recruitment will be used for employment recruitment purposes only, and not for any other purpose.

Job Description

Senior Manager, Supplier Quality and Quality Management Systems (Remote)

Are you looking to make your next career move? CellCarta, a Contract Research Organization, is hiring a Senior Manager, Supplier Quality and Quality Management Systems to join our dynamic team. In this role, you will have the opportunity to use your expertise and skills to ensure our services meet the highest industry standards. Join a team of talented individuals committed to making a positive impact on human health and well-being. Apply today and take the first step toward an exciting new career with CellCarta!

Summary

The Senior Manager of Quality Systems and Supplier Quality plays a critical leadership role in driving excellence and ensuring robust supplier quality systems that align with regulatory expectations and business objectives. This position is responsible for the strategic oversight, implementation, and continuous improvement of supplier quality processes and system frameworks.

Responsibilities

More specifically, you will participate in the following:

• Lead the development and execution of supplier quality strategies, ensuring alignment with corporate quality objectives and regulatory requirements. Oversee supplier performance, risk management, and compliance;
• Lead comprehensive supplier assessments, including risk evaluations, audits, and qualification questionnaires;
• Serve as the primary interface with corporate suppliers, fostering strategic partnerships and ensuring alignment with quality expectations. Maintain and negotiate quality agreements, ensuring they reflect current regulatory and operational requirements;
• Plan, execute, and oversee supplier audits, ensuring thorough documentation and follow-up;
• Contribute to the development and implementation of a robust third-party IT vendor management program, ensuring quality and compliance across digital platforms and services;
• Maintain and enhance systems for managing supplier complaints and Supplier Corrective Action Requests (SCARs), ensuring timely resolution and continuous improvement;
• Participate in ISO certification audits, including ISO 27001 and ISO 13485. Serve as a subject matter expert on Quality Management Systems;
• Perform and support QA review of Computer System Validation (CSV) deliverables related to CellCarta systems;
• Collaborate across CellCarta business units to develop harmonized policies, procedures, and work instructions. Lead initiatives to standardize key quality system SOPs that meet both site-specific and corporate requirements;
• Partner with internal stakeholders to identify and implement process improvements that enhance quality system performance, supplier oversight, and regulatory compliance;
• Manage and update corporate documents, including corporate supplier management materials, to present in management reviews.

Education

• Minimum BA/BS in science or health-related discipline.

Main Requirements

• Minimum of 5 years’ experience managing supplier quality systems. Ideal candidate will have specific experience in managing supplier quality and performing CSV reviews. Two years of audit experience is preferred;
• Knowledge of GCLP, GMP, and global regulatory frameworks to ensure supplier quality systems meet evolving compliance standards;
• Demonstrate proficiency in ISO 13485, ISO 15189, and CAP/CLIA requirements, serving as a key resource during audits and inspections;
• Lead supplier quality alignment initiatives, including the development and negotiation of quality agreements;
• Knowledge of compliance requirements for different stages of development; must have knowledge of applicable global regulations;
• Demonstrate exceptional written and verbal communication skills, with the ability to clearly articulate complex quality requirements and agreements to internal and external stakeholders. Influence cross-functional teams through clarity, credibility, and strategic insight;
• Excellent project management skills;
• Experience reviewing CSV documentation is preferred.

Working Conditions

• Regular working hours: Monday to Friday, 9:00 AM - 5:00 PM;
• This is a remote position; however, candidates must be located in Canada.

Benefits

We offer a wide range of benefits including:

• Competitive Wages;
• Vacation and Personal Days;
• Comprehensive Group Insurance Plans;
• RRSP Contribution with Employer Matching;
• Employee Annual Incentive Plan (EAIP);
• Dialogue Telemedicine Service and Employee Assistance Program (EAP);
• Referral Program;
• Career Advancement Opportunities.

About CellCarta

CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The Company operates globally with facilities located in Canada, USA, Belgium, Australia, and China.

Joining CellCarta means working with dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world! 

Join us as we make an impact on patient therapy!

The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc. and its affiliates (collectively, “CellCarta”). The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta.

CellCarta will only process that information which is necessary to evaluate your application. This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contact

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Company Description

Located in Hamilton, Canada, SANIHEALTH LABS is a leading and trusted full-service private label manufacturing company. With over 50 years of experience, we are dedicated to developing safe, premium quality products for clients in the skincare, personal health, and beauty industry, both locally and internationally.

Role Description

This is full-time/part-time on-site role for a Quality Control (QC) Volunteer, located in Hamilton, ON. The QC Volunteer will be responsible for:

Assist QC staff in performing routine sampling and testing of raw materials, in-process, and finished products.

Support inspection and monitoring of production activities to ensure adherence to GMP standards.

Help maintain accurate and complete QC records, logs, and test reports.

Participate in environmental monitoring, equipment calibration checks, and cleaning verification activities as needed.

Assist in reviewing batch records, labels, and packaging to confirm compliance with specifications.

Follow all safety and GMP requirements, including proper gowning, hygiene, and documentation practices.

Participate in internal audits and quality checks under the supervision of the Quality team.

Perform general laboratory support tasks (e.g., preparing solutions, labeling, organizing samples, and maintaining cleanliness of work areas).

Qualifications

• Strong interest in quality assurance/control, manufacturing, or regulatory compliance.
• Experience with Good Manufacturing Practice (GMP)
• Strong analytical and problem-solving skills
• Excellent attention to detail and organizational skills
• Ability to work on-site in Hamilton, ON
• Previous experience in the skincare, personal health, or beauty industry is a plus
• Bachelor's degree in a relevant field such as Chemistry, Biology, pharmacy, engineering, or a related field (students or recent graduates preferred).

WANT TO JOIN US?

kindly send us your resume We really appreciate your effort in applying for this position. However, only those who have been shortlisted for interviews will be contacted.

Job Description:

The Quality Control Auditor reports to the Quality Control Lead.

The Quality Control Auditor ensures that quality assurance is in accordance with expectations set out in the Quality Manual, Quality Procedures and Work Instructions and is equal to the requirements in the customer order or customer contract or the ISO9001:2015 & AS9100:D Standards. The Quality Control Auditor provides leadership in quality issues.

Knowledge, Skills & Abilities:

• Performs on Machine quality auditing for first off inspections.
• CMM operation proficiency is mandatory.
• CMM beginner programming experience is a must: Calypso
• Master proficiency reading blueprints, mechanical drawings, GD&T specifications and measuring features & characteristics in physical components to verify & validate its conformance by using metrology instruments (durometers, bore/profile/high/roughness, angle/radius gauges, micrometers, dial indicators, Gage maker, mic track, optical-laser scanning probing arms, etc.).
• Proficient in both measuring units' systems: Imperial & International System of Units (SI).
• Master proficiency measuring element by element API Tubing & Casing (T&C) and Rotary Shouldered Connections (RSC) threads.
• Verifies & validates processes and product conformance via Inspection Receiving, First Offs, Final Inspection, Process & Dock audits, testing.
• Identifies and records non-conformances and participates with the multidisciplinary team to identify Root Cause, Corrective & Preventive Actions.
• Submits recommended solutions to Quality problems and Manufacturing issues.
• Verifies correction of nonconforming items. Controls further processing of nonconforming items until the deficiency or unsatisfactory conditions have been resolved.
• Ensures that personnel understand inspection procedures and are fully qualified to perform these inspections.
• Prepares inspection records required in advance so that inspections can be processed in a timely and efficient manner.
• Ensures that personnel carry out inspections and testing according to stated procedures.
• Collects, inspects, and maintains all quality records & statistical data for accuracy.
• Maintains inspection/test equipment and ensures that it is accurate and calibrated to stated procedures.
• Ensures corporate assets and property are actively protected and safeguarded and liabilities and errors are minimized.
• Other duties as directed by Quality Control Lead.

Key Standards for Role:

• AS9100:D
• ISO 9001:2015
• ISO 10012:2003
• IATF

Qualifications & Requirements:

• 5+ years of experience as Quality Control Auditor in a manufacturing environment preferred
• Engineering designation preferred.
• Bachelor of Engineering degree (4+ years) advantageous

Position Description
At a Glance
Legrand
has an exciting opportunity for a Quality Control Inspector to join the Power-Bus-Way Team in Mississauga, ON.

The Quality Control (QC) Inspector is responsible for performing quality checks on incoming raw materials, in-process components, and finished products; This role ensures that all items meet required specifications and standards prior to approval for use or shipment. The QC Inspector works closely with the production and quality teams to identify and resolve quality-related issues in a timely and effective manner.

Key Responsibilities

• Carry out quality assessment measures of all finished products, incoming raw materials, supplied materials, and components.
• Thoroughly review plans, specifications, and blueprints to understand product requirements.
• Monitor production operations to ensure they meet quality and production standards.
• Recommend adjustments to the assembly or production process when necessary.
• Measure products using tools such as rulers, tape measures, calipers, combination squares, and other instruments, ensuring all tools are calibrated to standard references.
• Operate electronic inspection and software-based equipment for accurate assessments.
• Reject non-conforming incoming materials/components/painted boxes and report issues promptly to relevant personnel.
• Resolve quality-related issues while adhering to tight deadlines.
• Document inspection processes, including detailed reports and performance records.
• Recommend improvements to production processes to maintain quality standards.
• Guide the production team on quality issues to improve overall product quality.
• Monitor and inspect the production process at various stages.
• Accept or reject finished items based on inspection results.
• Remove defective products and materials from production or shipment.
• Report all inspection-related issues, including quality, quantity, and design discrepancies.
• Inspect, test, or measure materials or products during production.
• Collaborate with Management and QA in determining when a Non-Conformance Report (NCR) should be issued.
• Assist in the creation and documentation of NCRs.
• Perform other duties as assigned.

Qualifications
Qualifications

• High school diploma or GED required; Technical certification or associate degree in a related field (e.g., manufacturing, mechanical, or industrial technology) is a plus
• 2+ years' experience in quality inspection, preferably in a manufacturing or production environment
• Previous experience with quality management systems.
• Able to work expected hours of: 7:00am - 4:30pm Monday - Thursday, 7:00am - 12:00pm Friday.
• Flexibility to cover other shifts would be an asset
• Strong attention to detail and ability to identify defects.
• Good math skills for reporting data, measuring, calibrating, and interpreting specifications.
• Critical thinking skills to address production problems and propose quality improvements.
• Physical stamina and the ability to stand for extended periods.
• Proficient in reading technical drawings, documents, and manuals.
• High motivation to ensure products meet the highest standards.
• Experience in calibrating measurement tools and equipment.
• Computer literacy, including proficiency in Microsoft Excel, Word, and report preparation.
• Ability to learn and adapt to new software tools and digital systems

Company Info
About Legrand
Legrand is the global specialist in electrical and digital building infrastructures. Our comprehensive offering of solutions for residential, commercial, and data center markets makes us a benchmark for customers worldwide. We harness technological and societal trends with lasting impacts on buildings with the purpose of improving life by transforming the spaces where people live, work , and meet with electrical and digital infrastructures and connected solutions that are simple, innovative , and sustainable. Legrand is a global, publicly traded company listed on the Euronext ( Legrand SA EPA: LR ). For more information, visit

About Legrand North And Central America
Legrand, North & Central America (LNCA) is a leader in the AV, Lighting & Controls, Electrical , and Data Center markets . LNCA offers comprehensive medical, dental , and vision coverage, as well as distinctive benefits like a high employer 401K match, paid time off (PTO) and holiday pay, short-term and long-term disability benefit plans, above-benchmark paid maternity and parental leave, bonus opportunities in accordance with the Company's incentive plans, paid time off to volunteer, and an active/growing Employee Resource Group network. For more information, visit

About Legrand's Electrical Wiring Systems Division
Legrand's Electrical Wiring Systems (EWS) division provides the most complete line of residential, commercial, and industrial electrical wiring devices in the world. Through commitment to innovation and quality, EWS maintains the position of industry leader in wire and cable management and wiring devices categories, specializing in raceways, flexible floor, open space and outdoor power solutions, wire mesh cable trays and systems, and designer switches and outlets. With this comprehensive offering, EWS serves a range of exciting vertical markets, including commercial office and commercial interior, data centers, education, healthcare, hospitality, manufacturing, mixed-use developments and residential. For more information, visit wiring devices

Equal Opportunity Employer

Inspection & Monitoring

• Conduct daily site inspections of civil works including excavation, concreting, formwork, reinforcement, backfilling, roadworks, and finishing
• Verify that construction activities comply with project specifications, drawings, and applicable codes (e.g., CSA, ASTM, ACI, AASHTO, or local standards)
• Inspect and record quality of materials delivered to site (cement, aggregates, steel, concrete, etc.)
• Monitor batching, mixing, placement, curing of concrete, and other critical civil operations
• Ensure proper compaction, levels, alignment, and tolerances for earthworks and structural works

Documentation & Reporting

• Maintain daily inspection logs, checklists, and quality records
• Prepare Non-Conformance Reports (NCRs) when work does not meet specifications and follow up on corrective actions
• Verify and maintain records of test results (soil compaction, slump test, cube/cylinder compressive strength, asphalt density, etc.)
• Assist in preparing quality reports for submission to the client/consultant

Compliance & Coordination

• Ensure contractors implement approved Inspection & Test Plans (ITPs), Method Statements, and Quality Control Procedures
• Coordinate with site engineers, contractors, and third-party labs for material and field testing
• Support internal and external audits of quality systems
• Ensure compliance with safety regulations while performing inspections

Problem-Solving

• Identify potential quality risks and recommend preventive measures
• Stop work (if authorized) in case of critical quality non-compliance until corrective action is taken
• Provide technical support to construction teams on quality-related matters

Requirements

• Diploma or Bachelor's degree in Civil Engineering, Construction Management, or related field
• Minimum 3-7 years of experience in civil construction quality inspection (depending on project scale)
• Strong knowledge of civil construction standards, specifications, and testing procedures
• Familiarity with QA/QC documentation and ISO 9001 quality management systems
• Proficiency in MS Office (Word, Excel) and basic understanding of project management software
• Attention to detail, problem-solving skills, and ability to work independently
• Effective communication skills to coordinate with contractors, consultants, and clients