GE

Computerized Systems Validation Specialist

Montréal, Québec
On-site
Full-time
No salary postedYesterday
Employment type
Full-time · On-site
Posted
November 4, 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 Le Groupe Uni3T est une société informatique jeune et dynamique qui est active dans les secteurs des sciences de la vie et de l'industrie pharmaceutique. L'entreprise est née d'une volonté de réunir et d'unifier sous un même toit une expertise complète dans le domaine des sciences de la vie. Notre mission est d'améliorer l'accès aux soins et aux produits de santé en fournissant des services de consultation et des solutions technologiques aux entreprises des scien…

This role is based in Quebec. GenAIz 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 Computerized Systems Validation Specialist 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 computerized systems validation
  • Knowledge of pharmaceutical or life sciences industry
  • Understanding of GxP regulations and compliance
  • Ability to develop and execute validation protocols
  • Technical documentation and reporting skills

Fit check

Is this role right for you?

Top skills this posting asks for:

  • Computerized Systems Validation
  • GxP Compliance
  • CSV Documentation

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What you'll do

  • Validate computerized systems in life sciences and pharmaceutical environments
  • Develop and execute CSV protocols and documentation
  • Ensure compliance with regulatory requirements and GxP standards
  • Test and validate system functionality and performance
  • Collaborate with IT teams and business stakeholders
  • Document validation activities and maintain compliance records

What you'll need

  • Experience in computerized systems validation
  • Knowledge of pharmaceutical or life sciences industry
  • Understanding of GxP regulations and compliance
  • Ability to develop and execute validation protocols
  • Technical documentation and reporting skills
  • French language proficiency (based on job posting language)

About the Company

GE

GenAIz