This role requires a minimum of 40% 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: 9236
Employment status: Temporary full-time
Position's anticipated start date: 2026-10-19
Position's anticipated end date: 2028-04-18
Salary/Rate of pay: $86,400 - $101,700
Application deadline: 2026-09-30
- 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.About the roleCanadian Blood Services is looking for a
Temporary Full-time Regulatory Affairs Associate to join our dynamic
Quality and Regulatory Affairs team.
The
Quality and Regulatory Affairs division is responsible for providing daily support and subject-matter expertise to Canadian Blood Services in regulatory and quality matters, helping the organization to thrive as a biologics manufacturer and provider of transfusion and transplantation services.
In this role, you will integrate and apply your knowledge of domestic and international regulations governing all aspects of Canadian Blood Services' biological products (fresh blood products, plasma protein products, stem cells, tissues and organs) and services.
Formula for success- Leveraging your expertise in compliance management, you will, assist in the development, implementation, and continuous improvement of the national Regulatory Submissions process as it relates to submissions.
- Harnessing your proficiency in regulatory oversight, you will develop, review, and evaluate regulatory filings for submission to regulatory authorities.
- Drawing on your acumen in governance and compliance, you will participate in the review of change requests and customer letters submitted by the organization.
- Leveraging your understanding of industry protocols, you will participate in reviews of industry regulations and standards.
- Harnessing your mastery of statutory compliance, you will provide interpretation of regulations and standards.
- Drawing on your aptitude for regulatory navigation, you will assist in the definition, collection, analysis, and review of performance monitoring metrics.
Desired education and skills- Bachelor's degree in science (biology, chemistry, microbiology, immunology, medical technology).
- Minimum of 2 years' regulatory experience.
- Knowledge of domestic and international regulatory requirements, specific to fresh blood components, stem cells, tissues & organs.
- Thorough understanding of Good Manufacturing Practices.
- Demonstrated organizational, analytical, problem solving, time management and decision making skills are required.
- Ability to work on cross-functional teams and the ability to communicate effectively, verbally and in writing, with diverse audiences and personnel.
- Proficient in writing and editing technical documents.
- Respect for the sensitivity and confidentiality of documents received and reviewed.
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 a hybrid environment with requirements to be onsite at Canadian Blood Services location 40% of the time.
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.#LI-HYBRID
#LI-MB1
#LI-Ontario
#INDCBS
