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Quality Assurance Associate

  • Winnipeg, MB, R3E 3R4, Canada
  • Vancouver, BC, V6H 2N9, Canada

Salary/Rate of pay: $86,400 - $101,700

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Job details

Pay
Salary/Rate of pay: $86,400 - $101,700
Apply by
Working hours
37.5 hours a week
Positions available
2
Posting language
English
Posted

Original job description

This role requires a minimum of 60% - 80% on-site presence. Additional on-site work may be required based on business needs. On-site expectations are subject to change and may be adjusted on a temporary or permanent basis.

Job posting ID: 9440

​Employment status: Regular full-time
Position's anticipated start date: 2026-12-07 
Number of positions available: 2 

Salary/Rate of pay: $86,400 - $101,700

Application deadline: 2026-11-17 

  • This external job posting may close earlier than the advertised deadline. We encourage you to apply as soon as possible.
  • We recommend you save a copy of the job posting for reference throughout the recruitment process.

Application requirements:

  • Your up-to-date resume.
  • Job specific cover letter.

Do you currently work for Canadian Blood Services? All employees must apply via the internal career page.

Together, the work we do connects people and changes lives - including your own. 

Be part of a dynamic, collaborative and caring organization committed to saving and improving lives. Thousands of patients depend on us every day for reliable access to safe blood, plasma, stem cells and organs and tissues.

About the role

Canadian Blood Services is looking for 2 Regular full-time Quality Assurance Associates (QAAs) to join our dynamic Quality Assurance team in Winnipeg, Manitoba and Vancouver, British Columbia.

In this role, you will be providing the organizational assurance that we meet safety, quality identity, purity, potency and accessibility requirements of our products and services.

You will utilize your knowledge of Good Manufacturing Practices (GMP), this includes Blood Regulations as defined by Health Canada, CSA Blood and Blood Component Standards as well as relevant Cell, Tissues and Organs (CTO) regulations and standards as well as the theory and application of quality systems elements to the products and services provided by Canadian Blood Services.

Formula for success

  • Utilizing your expertise in Quality Assurance, you will ensure compliance and quality by maintaining controlled processes and applying Quality Management System principles across deviations, document management, retrieval/recall, validation, change control, audits, training, and corrective and preventive actions (CAPA).
  • Leveraging your excellent communication skills, you will educate staff as to "why" GMP, as defined by Canadian Blood Services Quality Management System, are necessary and how these ideologies apply to the activities Canadian Blood Services undertakes.
  • Drawing from your analytical and problem-solving skills, you will monitor and enhance product and service quality by analyzing data, conducting root cause investigations, and tracking improvements.
  • Leading and supporting audit activities for internal/external audits, accreditation assessments, and Health Canada inspections, including inspection readiness activities, ensuring timely completion of assigned corrective actions within agreed timelines.
  • Act as a subject matter resource for Testing quality processes by providing coaching, informal training, and knowledge-sharing sessions on GMP, Good Documentation Practices, investigations, and risk-based decision making.
  • Identify recurring quality issues, documentation gaps, and potential risks and share recommendations to support continuous improvement.
  • Performing all work in accordance with Canadian Blood Services Corporate Health and Safety Policies and Procedures, you will contribute to a safe and compliant work environment.

Desired education and skills

  • Completion of post-secondary education in a relevant discipline or equivalent experience.
  • Minimum 10 years' experience in a GMP manufacturing or pharmaceutical environment.
  • Minimum 5 years' experience in Quality Management and Continuous Improvement
  • Minimum of 3 years' experience in the quality assurance function of a testing or diagnostics program or organization following Good Manufacturing Practices is preferred.
  • In-depth knowledge of Health Canada, CSA, and AABB standards.
  • Technical skills in Quality Management Systems and Microsoft Office.

What we offer you

  • 4 weeks' vacation.
  • Annual performance award up to 6%. 
  • Comprehensive group health, dental and vision benefits for you and your family.
  • Defined benefit pension plan. 
  • Employee discounts, wellness program, professional resources. 

What you can expect

  • This role will work in an on-site environment with requirements to be on-site at Canadian Blood Services location 60% - 80% of the time/3 to 4 days of the week.
  • You will work 37.5 hours a week, with variable shifts, evenings and weekends with occasional on-call requirements.


If this role resonates with you, we encourage you to apply by providing your up-to-date resume. This could be your first step towards a meaningful and inspiring career. Come to work each day knowing that you save lives. 

We acknowledge that the work of Canadian Blood Services spans many Territories and Treaty areas across the country, and we are grateful for the Traditional Knowledge Keepers and Elders who have guided us in this important work. We recognize the land and waters that have inspired our work and offer gratitude to those Indigenous peoples on whose territory we work, live and play.

Diversity and inclusion play a vital role in ensuring health equity for patients across Canada. We are committed to reflecting Canada’s population in our organization and fostering an environment where all employees can be their authentic selves, with equal opportunities to succeed and contribute.

Canadian Blood Services may use an Artificial Intelligence (AI) tool to support the screening stage of its recruitment process. All AI use is performed in accordance with our privacy policies. AI supports the screening process; hiring leaders retain discretion over which applications move forward.

We thank all applicants for their interest. However, only those considered for an interview or those invited to participate in an assessment will be contacted. Emails are sent directly from our system, to ensure you receive them please add donotreply@blood.ca and system@successfactors.com to your safe senders list.

Applicants who require accommodation should discuss their needs with us.

More about this job

Responsibilities

The Quality Assurance Associate ensures organizational compliance with safety, quality, and regulatory standards by maintaining controlled processes and applying Quality Management System principles. They also lead audit activities, conduct root cause investigations, and provide coaching on GMP and documentation practices to support continuous improvement.

Requirements

Candidates must have post-secondary education and at least 10 years of experience in a GMP manufacturing or pharmaceutical environment. Proficiency in Quality Management Systems, Health Canada regulations, and CSA/AABB standards is essential for this role.

Skills

  • Quality Assurance
  • Good Manufacturing Practices
  • Quality Management Systems
  • Compliance
  • Root cause investigation
  • Audit support
  • Risk-based decision making
  • Document management
  • Corrective and preventive actions
  • Data analysis
  • Communication
  • Problem-solving
  • Validation
  • Change control
  • Coaching
  • Training

Benefits

  • 4 weeks' vacation
  • Annual performance award
  • Comprehensive group health benefits
  • Dental benefits
  • Vision benefits
  • Defined benefit pension plan
  • Employee discounts
  • Wellness program
  • Professional resources

Visa sponsorship

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Categories

  • Healthcare
  • Science & Research
  • Manufacturing
  • Management & Leadership

Keywords

  • Quality Assurance
  • GMP
  • Good Manufacturing Practices
  • Health Canada
  • CSA Blood and Blood Component Standards
  • CTO
  • Quality Management System
  • Deviations
  • Document management
  • Retrieval/recall
  • Validation
  • Change control
  • Audits
  • CAPA
  • Root cause investigation
  • Testing
  • Diagnostics
  • AABB
  • Microsoft Office
  • Pharmaceutical
  • Continuous Improvement
  • Compliance
  • Risk management
  • Health and Safety
  • Manufacturing

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