Quality Assurance and Regulatory Affairs Manager
- Employment type
- Full-time · On-site
- Posted
- October 15, 2026
- Province
- Quebec (QC)
Hiring confidence: Sparse posting · 22/100
This posting is missing most of the signals we look for, or shows patterns common to listings that are not actively being filled. Check with the employer before applying. How this is scored
Job Overview
This role is based in Quebec. Eli Health is hiring for this full-time position through Jobily, where you can check how well your resume matches the posting before you apply.
Market context
About this role in Quebec
Average salary for Quality Assurance and Regulatory Affairs Manager in Quebec
We do not have a salary benchmark for this title in Quebec yet. The posting does not state a salary either.
NOC code
This posting has not been matched to a NOC 2021 unit group yet. Use the NOC finder to identify the code from the duties listed above.
Typical qualifications for Canadian employers
- Experience in Quality Assurance and Regulatory Affairs
- Knowledge of FDA regulations and medical device compliance
- Understanding of quality management systems
- Documentation and record-keeping skills
- Experience with regulatory submissions
Fit check
Is this role right for you?
Top skills this posting asks for:
- Quality Assurance
- Regulatory Affairs
- Compliance
Jobily reads your resume against this posting and scores the fit — the skills you already have, the gaps, and what to change before applying. Signed-in Premium members see the score at the top of this page.
Scan your resume to see your fitKeep looking
Similar jobs
- SP
Sperry Rail
Copy of Technicien/Apprenti Certifié en Détection des Défauts de Rail (RFD)
Montréal, Québec · On-site
- MD
MDA Space Canada
Intermediate Technician, Maintenance & Calibration - Evening Shift
Baie-d'Urfé, Montréal · On-site
- SK
Skyservice Business Aviation
Level II Technician, NDT (Non- Destructive Testing)
Dorval, Montréal · On-site
What you'll do
- Manage quality assurance processes
- Oversee regulatory compliance and affairs
- Ensure product meets regulatory standards
- Develop and maintain quality documentation
- Coordinate with regulatory bodies
- Manage product testing and validation
- Support product development lifecycle
What you'll need
- Experience in Quality Assurance and Regulatory Affairs
- Knowledge of FDA regulations and medical device compliance
- Understanding of quality management systems
- Documentation and record-keeping skills
- Experience with regulatory submissions