214 Chief Quality Officer jobs in Canada

• Work Term: Permanent
• Work Language: English
• Hours: 35 to 44 hours per week
• Education: College, CEGEP or other non-university certificate or diploma from a program of 1 year to 2 years
• Experience: 2 years to less than 3 years
• or equivalent experience
• Tasks
  
• Develop and conduct production, inventory and quality assurance programs
• Inspect processes
• Conduct work measurement or other studies
• Collect and compile operational or experimental data
• Collect and analyze data and samples
• Assist in preparing estimates, schedules, specifications and reports
• Read blueprints and drawings
• Certificates, licences, memberships, and courses
  
• Certification by a provincial or territorial association
• Computer and technology knowledge
  
• MS Excel
• MS Outlook
• MS PowerPoint
• MS Word
• MS Windows
• Area of specialization
  
• Development of quality assurance programs
• Work planning, estimating, measuring and scheduling
• Security and safety
  
• Criminal record check
• Transportation/travel information
  
• Travel expenses not paid by employer
• Public transportation is available
• Work conditions and physical capabilities
  
• Fast-paced environment
• Work under pressure
• Attention to detail
• Ability to distinguish between colours
• Sitting
• Combination of sitting, standing, walking
• Standing for extended periods
• Personal suitability
  
• Efficient interpersonal skills
• Excellent oral communication
• Excellent written communication
• Initiative
• Organized
• Team player
• Values and ethics
• Screening questions
  
• Are you available for the advertised start date?
• Are you currently legally able to work in Canada?
• Do you currently reside in proximity to the advertised location?
• Do you have previous experience in this field of employment?
• Do you have the above-indicated required certifications?
• Green job
  
• Involves duties and responsibilities that lead to positive environmental outcomes
• Health benefits
  
• Dental plan
• Health care plan
• Vision care benefits

Job Title: Quality Assurance (QA) Personnel

Conduct inspections and tests to ensure product or service quality meets internal standards and customer expectations.

Identify, document, and track quality issues or defects.

Collaborate with production, development, or operations teams to resolve quality-related issues.

Maintain accurate QA documentation and reports.

Ensure compliance with relevant regulations and standards (e.g., ISO, GMP, etc., if applicable).

Recommend improvements to existing QA processes and procedures.

Participate in audits and support internal/external assessments.

High school diploma or equivalent required; a degree or certification in a relevant field is a plus.

Previous experience in a quality assurance role preferred.

Strong attention to detail and problem-solving skills.

Familiarity with QA tools, techniques, and industry best practices.

Good communication and teamwork abilities.

Ability to work independently and manage time effectively.

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 Title:
Quality Assurance Specialist

Location:
Toronto, Canada

Job Summary

The Quality Assurance Specialist plays a key role in maintaining and improving operational standards within JD Sports Canada's distribution centers. This role ensures that all warehouse activities align with company policies, compliance requirements, and service-level agreements. The Quality Assurance Specialist is responsible for conducting audits, identifying risks, and supporting continuous improvement initiatives to drive accuracy, efficiency, and consistency across operations.

Key Responsibilities

• Monitor daily warehouse activities to ensure compliance with company policies, standard operating procedures, and service-level agreements.
• Conduct regular audits of inbound, outbound, and inventory processes to validate accuracy, safety, and adherence to quality standards.
• Identify and document areas of non-compliance or risk, and work with Warehouse Managers, Supervisors, and Team Leads to implement corrective and preventive actions.
• Develop and maintain quality metrics, dashboards, and reports to track performance trends and highlight opportunities for improvement.
• Partner with Operations, Supply Chain, Loss Prevention, Merchandising, Planning, and Buying teams to resolve recurring issues and support cross-functional process improvements.
• Lead training sessions and provide ongoing coaching to warehouse staff on quality standards, compliance requirements, and best practices.
• Assist in the development and refinement of standard operating procedures, ensuring they remain up to date and aligned with industry and company standards.
• Support incident investigations and root cause analysis to prevent reoccurrence of issues.
• Act as a liaison between the distribution centers and corporate teams on matters related to quality, compliance, and operational risk.

Qualifications

• Minimum 3–5 years of experience in quality assurance, operations compliance, or process improvement within a warehouse, distribution center, or logistics environment.
• Strong understanding of quality management systems, audit processes, and regulatory compliance in a supply chain setting.
• Proven ability to analyze operational data, identify trends, and develop actionable recommendations.
• Excellent communication, interpersonal, and collaboration skills to influence stakeholders at all levels.
• Detail-oriented with strong organizational and time-management skills.
• Ability to balance independent work with cross-functional collaboration in a fast-paced environment.

Education

• Bachelor's degree in Supply Chain Management, Operations, Quality Assurance, or a related field, or equivalent work experience.
• Certifications in quality or process management (such as Six Sigma, Lean, or ISO standards) are considered an asset.

Location: Calgary, Alberta

Type of Employment: Permanent – Full time

About Us:

Northern RNA Inc. is a Canadian CDMO specializing in the production of nucleic acid products that support life-enabling work. Our goal is to work alongside our customers to provide scalable manufacturing capacity and to help them accelerate innovation in bringing their products from benchtop to bedside or field.

About Our Opportunity:

Quality Assurance Associate will be an individual who is seasoned in the field of Good Manufacturing Practices (GMP) manufacturing. This candidate will support NRNA's quality assurance team to and provide quality expertise. This Candidate will help to ensure compliance and continuous improvement of the Quality Management Systems.

Primary Responsibilities:

• Prepare, review, approve master documents, executed documents, and summary reports as applicable (i.e., Batch records, specifications, qualification/validation protocols, etc.)
• Prepare, review, approve deviations, CAPA, Change Controls, SOPs, etc. as applicable
• Support cross functional teams when issues arise. On-call support may be required.
• Conduct quality line clearance sign offs
• Coordinate/perform material release
• CoA/CoC review and approval
• Liaise with all departments to ensure products are released on time
• Work with team to maintain GMP in everyday practice
• Act as a mentor and coach for team members and new employees.
• Support Quality Head in all aspects of the Quality Management System
• Identify and implement process improvement to enhance systems and continuously improve
• Monitor and analyze quality metrics to identify trends and areas for improvement.
• Review and approve supplier qualification
• Support/host with internal/external audits
• Work with cross functional teams for validation activities associated with new equipment, processes, methods, or system upgrades.
• Provide quality oversight for activities such as design of systems and equipment to ensure that they comply with applicable regulations & International Standards.
• Additional duties as assigned

Education, Work Experience, Knowledge, and Skills:

Formal Education:

• Minimum Bachelor's degree in science (bioengineering, chemical engineering, bioprocess, biotechnology, cell biology, microbiology, chemistry etc.)

Work Experience:

• 5 years of experience in GMP production within the pharmaceutical, biotechnology, medical technologies, biologics, or similar industries.

  
  
• Experience working for a Contract Manufacturing Organization (CMO), a third-party testing facility, or a biotechnology company performing similar activities.

Knowledge and Skills:

• Strong English written and oral communication.
• Advanced understanding of quality management systems
• Strong knowledge and experience in GMP requirements.
• Sound knowledge of applicable regulatory frameworks
• Independent, detail-oriented, self-starter with excellent analytical skills, high level of critical thinking, and the ability to multitask and succeed in a team environment.
• Excellent time management
• Experience in establishing customer-facing organizations and service models.
• Demonstrated initiative and the ability to oversee delivery of high-quality outcomes.

Working conditions:

• Physical environment: Majority of time spent in a comfortable position with frequent opportunity to move about at will.
• Physical effort: May have to lift/move materials during release, move documents
• Sensory Attention: Work activities involve need to concentrate on a variety of sensory inputs specifically visual attention for long durations, requiring close attention several times daily.
• Mental Pressures: High – Must have strong attention to details, be able to make decision with information present. Be able to approve documents and risk assess as required

What we offer?

We offer a highly competitive salary and company-paid benefits. Additionally, there are excellent opportunities for learning and growth while working alongside our teams of experts who are bright, collegial, and highly motivated and who are on the cusp of the mRNA vaccine science and technology era.

Benefits:

Northern RNA Inc. offers its employees a wide range of benefits such as Health, Dental, Basic Life Insurance, General Illness (Long Term Disability), Vacation, Performance Bonus, on-site parking and Accidental Death and Dismemberment.

Additional Information:

• Location for this position is in Calgary, Alberta. Candidates must be located within commuting distance or be willing to relocate to this area. Canadian citizens and those legally entitled to work in Canada are encouraged to apply. We are currently unable to sponsor.

Northern RNA Inc. is committed to a diverse and inclusive workplace. Northern RNA Inc. is an equal opportunity employer and does not discriminate on the basis of race, religion, color, national origin, gender, gender identity, gender expression, sexual orientation, age, marital or veteran status, pregnancy or disability or other legally protected status. In accordance with applicable law, we make reasonable accommodations for applicants' and employees' religious practices and beliefs, as well as any mental health or physical disability needs.

Offer of employment is conditional upon the completion of all applicable background checks and confirmation of credentials, the results of which must be satisfactory to the employer. We thank all applicants for the interest, however, only those selected for an interview will be contacted.

Job Types: Full-time, Permanent

Pay: Up to $70,000.00 per year

Benefits:

• Dental care
• Extended health care
• On-site parking
• Paid time off
• Vision care
• Wellness program

Ability to commute/relocate:

• Calgary, AB T2A 7H8: reliably commute or plan to relocate before starting work (required)

Education:

• Bachelor's Degree (required)

Experience:

• GMP: 5 years (preferred)

Work Location: In person

Summary

Assures product quality and safety by monitoring and auditing raw ingredients and finished products, as well as all operational procedures in food manufacturing. Verifies all daily HACCP and SQF and production records to ensure they are complete and accurate.

Raw ingredients :

Inspects and evaluates raw incoming ingredients by verifying conformance to specifications.

Follows up with the decision to accept or reject the raw product by reviewing CoA. Initiates product returns as needed.

Communication with suppliers on nonconformance of specifications and/or other quality issues and coordinating with material management staff.

Finished products :

Coordinates taste panels and assess the finished product. Prepares reports related to finished product quality as needed.

Updates quality attributes for new products and as required.

Actively investigates product deviations and recommends follow-up action plans to manufacture.

Conducts random quality and food safety inspections on products and/or procedures to ensure standards are maintained.

Investigate consumer complaints and develop an action plan.

Validate production instruments and tools as per HACCP requirements.

Sanitation & Food Safety:

Conducts scheduled sanitation inspections as per HACCP guidelines.

Conducts onsite verifications of equipment sanitation.

Verifies critical control point information needed for early release.

Maintains sanitation of test kitchen area.

Performs swab tests to monitor equipment cleanliness (environmental swabbing, allergen swabbing).

Provides relief for bacteriological testing of finished products and assessment of lab results.

Recommends operating methods and procedures or equipment designed to eliminate operating problems and improve product quality.

Communicates, trains, and conducts on-site with staff on established Food Safety Management System procedures.

Conducts inspections including operational, coding monitoring, storage, equipment, and utensils on a daily/ monthly basis.

Education and/or Experience

College diploma in Applied Food Science or equivalent and 1-3 years related experience; or equivalent combination of education and experience.

Experience with HACCP or SQF is required.

Job Types: Full-time, Permanent

Pay: $19.00-$27.00 per hour

Benefits:

• Casual dress
• Company events
• Dental care
• Disability insurance
• Extended health care
• On-site parking
• Paid time off
• Store discount
• Vision care

Experience:

• Quality assurance in food processing: 2 years (required)

Work Location: In person

Would you like to put your quality assurance analyst skills to work on a large-scale project in collaboration with an exciting client Are you skilled at planning, organizing, and carrying out software testing? Do you enjoy sharing ideas, exploring new approaches, and taking on stimulating challenges? If this sounds like you, we can't wait to meet you Join an outstanding team and become part of a community of professionals who are truly passionate about software development.

• Review business requirements, system requirement specifications, design and other project documents to ensure adequate test coverage;
• Develop testing strategies, and identify tools and processes to optimize overall quality assurance activities;
• Create a complete quality assurance validation cycle;
• Create and update testing plans according to project progress;
• Run test scenarios and participate in quality assurance validation;
• Identify and document bugs found during testing;
• Contribute to advance the internal QA practice by sharing knowledge with others, harmonizing QA processes and defining good practices and guidelines;
• Participate in customer meetings and present QA work.

• Bilingual (French and English, written and spoken)*
• Attention to detail
• Analytical and resourceful
• User-oriented perspective
• Ability to do manual testing;
• Ability to develop test cases;
• Experience with bug tracking tools (ex: Azure DevOps, Xray for Jira);
• Experience in API testing;
• Significant experience with manual testing;
• Knowledge of Agile methodology and solid understanding of the software development life cycle (SDLC)
• Asset: Experience with database testing
• Asset : Experience with test automation tools (Selenium or equivalent)
• Asset: Experience with version control (Git, Azure DevOps or equivalent).

• Flexible work arrangements (remote, hybrid, or in-person), because what truly matters is not where you are, but what you do.
• Salary range: $65 000 to $2 000, based on a 37.5-hour workweek.

• 100% hybrid work policy, because it's usually not about where you are, but what you do;
• In addition to vacation weeks, our HUG program allows for unlimited leave when things aren't going your way, plus additional vacation days during the Christmas period;
• DPSP-RRSP program with employer contribution;
• Complete group insurance plan, including telemedicine;
• Spiri-Flex program to ensure a healthy body, mind and environment, we offer a total reimbursement of 300 per year for expenses related to health, wellness or work at home.

Work Environment

We believe work-life balance is essential. We make this possible through a flexible work organization and a personalized working style. Whether you're at the office or in your location of choice, what matters most is the impact of your work, not where you're doing it from.

About Us

At Spiria, we're a team of over 150 professionals across Canada. For more than 20 years, we've been building custom software solutions driven by a strong commitment to code quality, technological excellence, collaborative creation, and customer satisfaction.

• Bilingualism is essential for this role. The person in this role will need to collaborate with internal and external clients across North America in both French and English for all tasks.

At Spiria, we believe diversity is a major strength. We therefore adhere to the principle of employment equity and encourage applications from women, visible minorities, Indigenous people, persons with disabilities, LGBTQIA2S+ individuals, and other marginalized communities.

AI Notice

Our recruitment tools use AI to assist in the initial screening of applications, but never replace the intuition and expertise of our recruitment teams.

Combining the spirit of achievement with human and social values has always been a priority at SciCan. Add to this our proven track record of innovation, high quality and dependability, and you'll find a powerful combination that has ensured our growth as a company. We maintain our position as a leader in the health care industry by using a management structure that balances trusting relationships with a creative, dynamic environment.

Being a member of the SciCan family means taking an interest in exploring new paths and using your leadership and strategic planning skills. If you thrive in an exciting, active environment and value quality of life as much as quality of work, we'd like to hear from you. Feel free to send us your resume to if you're interested in pursuing an opportunity with SciCan in the future.

This position will be responsible for executing a range of quality assurance activities, including but not limited to; managing the calibration and maintenance program for tools and measuring equipment; coordinating and conducting final inspection procedures for finished products; monitoring and resolving open Temporary Deviation Notices (TDNs); and organizing training initiatives for newly onboarded personnel. This role plays a critical part in ensuring compliance with quality standards and supporting continuous improvement across the organization.

• Communication
• Problem Solving, Mathematical Reasoning
• Teamwork
• Result Focus
• Quality Oriented
• Accountability and Dependability
• Time Management
• Ethics and Integrity
• Adaptability/Flexibility
• Providing Consultation
• Creative and Innovative Thinking
• Enforcing Regulations
• Decision Making and Judgement
• Continual Learning
• Planning and Organizing

• Review, update, and maintain quality documentation including procedures, manufacturing instructions, and forms.
• Oversee the Calibration and Maintenance Program for all tools and measuring equipment.
• Notify relevant departments of upcoming calibration deadlines.
• Coordinate the shipment and receipt of equipment with external test and calibration facilities.
• Organize and perform final inspection activities for finished products in collaboration with QA personnel, in accordance with the production schedule.
• Assist in validating production processes to ensure compliance and efficiency.
• Facilitate supplier onboarding and manage periodic evaluations and re-evaluations.
• Collaborate with cross-functional teams to address product quality concerns and support related initiatives.
• Prepare and analyze production quality reports; investigate root causes of failures and recommend corrective actions.
• Develop and manage training programs for the Quality Assurance department.
• Conduct in-process inspections of finished products as scheduled.
• Monitor and resolve open Temporary Deviation Notices (TDNs).
• Develop and maintain various Quality departmental KPIs
• Investigate customer complaints and coordinate root cause analysis.
• Perform internal audits of the Quality Management System and supplier audits as required.
• Provide support and backup coverage for QA team members.
• Support various Quality projects as required
• Execute additional tasks as assigned by the Quality Assurance Manager to uphold the Quality Management System and departmental objectives.

• Degree in Quality Engineering or Engineering Degree plus Quality Certificate
• Minimum of 2 years related experience in a Medical Device manufacturing environment preferably with technology related products
• Extensive familiarity with ISO 13485, preferably the 2016 version; MDSAP experience and application an asset; MDR experience is an asset
• Internal auditing and risk management experience an asset
• Strong communication skills both verbal and written
• Ability to work in groups as well as independently with minimal supervision
• Strong analytical and problem-solving skills are essential
• Computer skills: MS Office, ERP (SAP preferred)
• Proven ability to deliver presentations and training, effectively and efficiently with clear communication skills and delivery

Join Jones Healthcare Group - Where Innovation Meets Purpose

At Jones, we're committed to the environment, our team, communities, and consumers, and we're inspired to make a meaningful impact through advanced packaging and medication dispensing solutions.

Learn more about us here:

Summary of position:

If you love ensuring products meet the highest standards and thrive in environments where precision matters, this role is for you.

If you get inspired by supporting teams to follow cGMP and quality processes that protect patients and consumers, you'll feel right at home here.

If you are driven by the challenge of solving problems, maintaining compliance, and keeping quality at the core of operations, you can make a real impact with us.

As a Quality Assurance Inspector, your responsibilities will include carrying out inspections using established procedures to ensure product quality, reviewing and verifying packaging operations, supporting production teams with compliance, and maintaining documentation in line with cGMP. You'll be an integral member of the Quality Assurance team, ensuring quality is at the forefront of every step of our packaging process.

More about your responsibilities:

• Production Start-Up: Participate in start-up meetings, confirm specifications for each job, and approve the production run.
• Line Clearance & Verification: Perform area clearances and cleaning checks, verifying that previous product and packaging materials are fully removed.
• Product & Materials Checks: Verify correct product, packaging, lot numbers, and control numbers against orders and release records.
• In-Process Inspections: Conduct sampling, inspection, and testing to ensure packaged product meets required specifications.
• Training & Support: Guide operators on sampling and testing requirements and promote adherence to quality plans.
• Documentation & Audits: Review and audit batch records, ensure results align with specifications, and support investigations into discrepancies with CAPAs and root cause analysis.
• Good Documentation Practices: Act as a champion on the shop floor, addressing issues and providing guidance to ensure traceability and compliance.
• Validation & Release: Carry out validation sampling and testing per protocol, document results, and support product release for both incoming and finished goods.
• Collaboration & Flexibility: Work closely with Production and QA teams to maintain a strong quality culture and take on additional duties as needed.

What you'll bring

• Values that mirror ours, from the Inside Out: Ingenuity, Nimble, Supportive, Inclusive, Driven, Empathetic
• High school diploma required; post-secondary diploma or bachelor's degree in a science-related field preferred.
• Additional training or certification in cGMP Quality Assurance is an asset.
• 1+ years of experience in quality assurance within a cGMP pharmaceutical environment preferred.
• Strong knowledge of cGMP and Good Documentation Practices (GDP).
• Excellent communication skills, with strong attention to detail and accuracy.
• Ability to manage time, prioritize tasks, and adapt to changing demands.
• Proficiency with Microsoft Office (Excel, Word, Outlook).
• Flexibility to work rotating shifts, including days, afternoons, midnights, and continental schedules.
• Experience within a pharmaceutical or food environment
• Understanding/familiarity of cGMP
• Experience within a regulated environment packaging/food/pharmaceutical (FDA, Health Canada)

We care about our colleagues, some benefits we offer are:

• A safe, respectful, diverse, and inclusive environment
• Competitive compensation and equitable people practices
• Comprehensive benefits and an RRSP program where we match up to 5% of your earnings
• Opportunities to grow and develop, alongside a supportive team
• Employee and family assistance program
• Referral bonuses
• Education reimbursement program
• Colleague appreciation events
• and more

Join us in shaping the future of healthcare Apply now to join our dynamic team and make a meaningful impact in a collaborative environment.

Please submit a resume and let us know why you are interested.

While we thank all candidates for their interest, only those selected for an interview will be contacted.

As part of our commitment to accessibility for all persons with disabilities, Jones Healthcare Group will, upon the request of the applicant, provide accommodation during the recruitment process to ensure equal access to applicants with disabilities. Please contact the Jones Human Resources department at about your needs, and we will consult with you to ensure suitable accommodation is provided.

For all feedback on equity and accommodation needs, please also contact the Human Resources department.