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Canadian Blood Services

Quality Control Associate

Brampton, ON, L6T 5M1, Canada
Ottawa, ON, K1G 4J5, Canada

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

Apply About employer

Applications open in a new tab.

Job details

Pay: Salary/Rate of pay: $86,400 - $101,700
Apply by: Nov 10, 2026
Working hours: 37.5 hours a week
Posting language: English
Posted: Nov 4, 2026

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: 9412

Employment status: Temporary full-time
Position's anticipated start date: 2027-01-05

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

Application deadline: 2026-11-10

This external job posting may close earlier than the advertised deadline. We recommend applying as soon as possible.

Application requirements:

Your up-to-date resume.
Job specific cover letter.
We recommend you save a copy of the job posting for reference throughout the recruitment process.

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 a Temporary full-time Quality Control Associate to join our dynamic Quality Assurance team for a term of 3 years.

The Quality Control Associate (QCA), within the Quality Control (QC) department, under the direction of the Quality Control Manager (QCM), supports the implementation and monitoring of the performance and activities of the Corporate QC Program. This program is used to fulfil regulatory requirements related to the manufacturing and testing of blood and blood components.

This position ensures, by means of sound application or Risk Management principles, the safety, efficacy and quality of all blood products, blood components and services offered by Canadian Blood Services through full compliance with Good Manufacturing Practices and all other applicable regulatory and legislative requirements.

The QCA, QC, ensures that the Corporate QC Program supports the requirements and standards for quality control in the manufacturing process. The QCA ensures that Canadian Blood Service sites have Operating Procedures necessary to perform inspection, product component testing, results evaluation, and reporting. The QCA Leverages the Quality Event Management program when required for product or process deviations and acts as a QC resource for the organization.

Formula for success

Working in a regulatory environment, you will develop, establish and maintain Canadian Blood Services' Corporate QC program and the Quality Control Component Testing database ensuring that the component QC program meets regulatory requirements, and all elements of the QC processes are consistent and controlled.
Leveraging your analytical and continuous improvement skills, you will collaborate with cross-functional teams to support initiatives that modernize Quality Control reporting processes, including the evaluation and implementation of data management, reporting, and data visualization solutions to improve efficiency, reduce manual data manipulation, and enhance access to quality performance metrics.
Drawing on your knowledge of investigation and inspection processes, you will develop and maintain the QC operating procedures for the inspection and release of incoming materials and supplies.
You will assist in the design, implement and manage the National Proficiency Testing Program.
You will assist the Quality Control Manager and the organization to monitor and improve the quality of its products by collecting and analyzing data to evaluate/demonstrate process control in manufacturing.
Utilizing your interpersonal and communication skills, you will provide ongoing guidance and support to site/functional staff in the application of the Corporate Quality Control Program in daily operations, QC and Corporate initiatives.

Desired education and skills

Completion of post-secondary degree in a related discipline from a recognized academic institution.
Minimum 3 - 5 years' experience within a GMP manufacturing or pharmaceutical environment.
Minimum of 1 - 3 years of Quality Management and Continuous Improvement experience.
Working knowledge of statistical analysis methods, SPC techniques and experience using software tools such as Minitab, JMP, SAS, or equivalent to analyze data, identify trends, and support quality and process improvement activities.
Experience with business intelligence, data visualization, or reporting tools (e.g., Power BI, Tableau, SQL, Alteryx, or similar platforms) is considered an asset.
In-depth knowledge of Health Canada, CSA, and AABB standards.
Knowledge of blood product manufacturing or lab testing experience is considered an asset.

What we offer you

Payment in lieu of vacation.
Annual performance award up to 6%.
Payment in lieu of benefits.
Defined benefit pension plan.
Employee discounts, wellness program, professional resources.

What you can expect

This role will work in an on-site presence with requirements to be on-site at Canadian Blood Services location 60% - 80% of the time/3-4 days of the week. Prefered location would be Brampton, ON or Ottawa ON.
Shift/hours - Monday to Friday, 37.5 hours a week/7.5 hours a day.
Travel requirements - travel will be required for onsite visits or occasonial meetings and training needs.

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.

(hashtags for LinkedIn (LI) and Indeed (IND) - delete these instructions
- keep all hashtags on separate lines
- select only one hashtag for each category
- change the hashtag's font colour to white, to prevent it showing on the posting
- pick either hybrid or onsite
- TAS with Recruiter Seat - pick your initials, this will associate the posting with your profile
- if you want the LinkedIn posting location to display a province choose one OR use the CBS Locations.xlsx (right click, open in new tab) document to add the city you would like posted, a location hashtag is not required if the posting only has one location
- Indeed *reach out to Lisa to sponsor the job*)

Apply About employer

More about this job

Responsibilities

The Quality Control Associate supports the implementation and monitoring of the Corporate Quality Control Program to ensure compliance with regulatory requirements for blood and blood component manufacturing. This role involves developing operating procedures, managing quality events, and collaborating with cross-functional teams to modernize reporting and data management processes.

Requirements

Candidates must possess a post-secondary degree in a related discipline and 3-5 years of experience within a GMP manufacturing or pharmaceutical environment. Proficiency in statistical analysis methods and experience with quality management and continuous improvement are required.

Skills

Quality control
Quality assurance
GMP manufacturing
Pharmaceutical environment
Continuous improvement
Statistical analysis
SPC techniques
Minitab
JMP
SAS
Data visualization
Power BI
Tableau
SQL
Alteryx
Risk management

Benefits

Payment in lieu of vacation
Annual performance award
Payment in lieu of benefits
Defined benefit pension plan
Employee discounts
Wellness program
Professional resources

Visa sponsorship

Not detected in the job text

Keywords

Quality Control
Quality Assurance
GMP
Pharmaceutical
Continuous Improvement
Statistical Analysis
SPC
Minitab
JMP
SAS
Data Visualization
Power BI
Tableau
SQL
Alteryx
Risk Management
Health Canada
CSA
AABB
Blood Product Manufacturing
Laboratory Testing
Regulatory Compliance
Quality Event Management
Proficiency Testing
Data Management

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