CL

Responsable Assurance Qualité Expert

Montréal, Québec
On-site
Full-time
No salary posted5 days ago
Employment type
Full-time · On-site
Posted
October 30, 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 is only part of this posting — the job board it came from publishes a short summary. Read the full posting.
Job Description Job Description Chez CLEIO, nous repoussons les frontières de l'innovation pour créer des produits médicaux et de hautes technologies qui changeront l'avenir. Notre équipe multidisciplinaire de plus de 60 experts en stratégie, design, ingénierie, développement applicatif, et bien plus encore, collaborent afin de contribuer au développement des produits technologiques. Nous travaillons tous ensemble pour développer des produits numériques et physiques qui auront un impact positif…

This role is based in Quebec. CLEIO 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 Responsable Assurance Qualité Expert 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

  • Expertise in Quality Assurance
  • Knowledge of medical device industry standards
  • Regulatory compliance experience
  • Leadership experience
  • Technical documentation skills

Fit check

Is this role right for you?

Top skills this posting asks for:

  • Quality Assurance
  • Medical Device Regulations
  • Testing & Validation

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What you'll do

  • Lead quality assurance initiatives
  • Ensure compliance with medical device regulations
  • Develop and implement quality standards and processes
  • Collaborate with multidisciplinary teams on product development
  • Conduct testing and validation of products
  • Manage quality documentation and risk assessments
  • Drive innovation within quality frameworks
  • Ensure positive impact of technological products

What you'll need

  • Expertise in Quality Assurance
  • Knowledge of medical device industry standards
  • Regulatory compliance experience
  • Leadership experience
  • Technical documentation skills
  • Multidisciplinary team collaboration experience

About the Company

CL

CLEIO